Teckro eliminates the barriers that stall clinical trials and frustrate research budgets and timelines. A single app for all clinical trial protocols, Teckro is the must have resource for centralized study communication and collaboration, enabling progress at pace and better patient care. Thousands of investigators around the world rely on Teckro for immediate answers anytime, anywhere. Available on Apple and Android devices, Teckro supports all phases, any trial setting, and every therapeutic area. A native Irish company, Teckro is headquartered in Limerick.

Technology

Teckro

You need 5+ years in clinical research and project management, strong stakeholder skills, attention to detail, and relevant degree or equivalent experience. PM training preferred.

You will manage client relationships, ensure timely delivery of products, develop use cases, track KPIs, and provide training while identifying issues and contributing to sales efforts.

Dublin

<div>
 About Teckro
 
 
 We founded Teckro to simplify and modernize clinical trials. In fact, thousands of clinical trial investigators and research site staff rely on Teckro to make the most informed decisions for their patients.
 
 
 That’s where you come in. We’re offering you a role with purpose. Your contribution at Teckro will lead to faster, safer and more efficient clinical trials. Quality of life will be improved. In the end, lives will be saved.
 
 
 Could you be our newest Teckronaut?
 
 
 Expectations include the ability to build relationships (internally and externally), identify client needs, deliver our strategic and innovative solutions, and ensure that client contracts are delivered on time and on budget. A program lead is responsible for ensuring a superior client experience and driving account growth. This experienced professional exhibits decision quality, action orientation, communication savvy, and resourcefulness to meet both Teckro and client needs. 
 What you’ll Do: 
 <ul> 
 <li>Ensure the ongoing successful and timely delivery of Teckro products and premium services to clients for the assigned programme/portfolio. Define use cases to support customer business</li> 
 <li>Oversee and ensure the timely and successful delivery of solutions both at implementation and throughout the trial’s lifecycle that align with service level agreements.</li> 
 <li>Establish and manage executive-level relationships with client decision makers and influencers.</li> 
 <li>Develop and manage governance model and issue escalation pathway for assigned client. </li>
 <li>Establish standards/operating framework that aligns with client needs/expectations to promote standardization and drive efficiency</li> 
 <li>Manage relationships with key existing clients through frequent communication, including formal and informal meetings and client visits.</li> 
 <li>Work with internal teams as well as external stakeholders to identify, monitor and manage risks during the development of the programme and adhere to change control process where applicable. </li>
 <li>Track, review and assess the implementation and ongoing Teckro KPIs for the programme and identify areas of improvement </li>
 <li>Working with the client, develop the business case and ROI metrics to demonstrate the value of the Teckro platform across the elements of speed, cost and quality. Ensure access to client data/metrics in order to develop the business case.</li> 
 <li>Regularly contribute ideas for innovation and product, quality, and process improvements </li>
 <li>Develop long-term relationships with your portfolio of assigned clients, connecting with key business development executives and other stakeholders.</li> 
 <li>Educate clients for assigned programmes on products, new solutions and best practices</li> 
 <li>Ensure that training is provided on Teckro products as needed to clients and new users at a programme level</li> 
 <li>Operate as the lead point of contact for all matters specific to the managed clients for the assigned programme/portfolio/client</li> 
 <li>Proactively identify issues in client service relationships, address these directly and intervene when necessary to ensure client satisfaction.</li> 
 <li>Being an active contributor of the sales team to reach and exceed the sales quota while achieving sales targets. </li>
 <li>Manage Account Plan development activities for assigned clients and own the development and delivery of the operational delivery plan</li> 
 <li>Participate in conferences and support other Marketing activities to share Teckro’s ROI and use cases for the platform</li> 
 <li>Participate in use case development for Teckro products by phase, stage of development, therapeutic area and study role.</li> 
 <li>Ability and willingness to travel (approximately 20-30%) </li>
 <li>Undertake other duties in-line with your role and business requirements as required and requested by the hiring manager.</li>
 </ul>
 
 The Ideal candidate will have: 
 <ul> 
 <li>Extensive clinical research and clinical trial experience required, preferably across various a variety of therapeutic areas. Minimum 5 years of clinical research experience.</li> 
 <li>Minimum of 5 years relevant project management experience, preferably in the Lifesciences, Clinical Research and Development space with experience in complex and critical projects</li> 
 <li>Possesses a forward-thinking approach to the management of various internal and external stakeholders. </li>
 <li>A proven ability to take ownership of projects and achieve required deliverables ensuring projects are delivered to the highest quality.</li> 
 <li>Excellent presentation and communication skills, and ability to demonstrate knowledge of the company products and technology to internal and external stakeholders</li> 
 <li>Highly motivated and organised individual, with particular attention to detail</li> 
 <li>Ability to work on one’s own initiative, whilst also being able to take direction</li>
 </ul>
 
 
 Qualifications Required: 
 <ul>
 <li>Degree in related field(s); or equivalent combination of relevant work experience and education</li> 
 <li>PM Training – e.g. Applied PM, Commercial PM, or equivalent combination of relevant work experience and education</li>
 </ul>
 
 
 Location and Travel: 
 (Dublin/Limerick) 
 <ul> 
 <li>Hybrid work option with the flexibility to work in our Irish offices located in Dublin or Limerick City. Currently this is set to 3 days per week onsite.</li> 
 <li>We also offer flexible start/ end times, allowing your schedule to suit your lifestyle</li> 
 <li>Willingness to travel internationally as required</li> 
 <li>Please note: Regrettably we cannot offer work permit/sponsorship or self-sponsorship for this role. Eligible applicants must already hold valid and legal work permit for Ireland</li>
 </ul>
 
 
 Teckro Benefits:
 
 
 <ul> 
 <li>25 days holidays</li> 
 <li>Pension</li> 
 <li>Healthcare</li> 
 <li>Life Insurance</li> 
 <li>Share Options</li> 
 <li>50% Maternity leave pay after capped length of service</li> 
 <li>Paid Paternity leave scheme</li> 
 <li>Bike to Work/ Tax Saver Scheme</li> 
 <li>Gym/Wellness Allowance</li> 
 <li>Sports and Social Club</li>
 </ul>
 
 
 We are always looking for amazing people to join our growing team. If you are curious, passionate and motivated, then we want to talk to you!
 
 
 By submitting your application, you agree that Teckro may collect your personal data for recruiting and related purposes. Teckro's Recruitment Privacy Statement explains what personal information Teckro may process, where Teckro may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Teckro’s use of your personal information.
</div>


 About Teckro
  
  
  We founded Teckro to simplify and modernize clinical trials. In fact, thousands of clinical trial investigators and research site staff rely on Teckro to make the most informed decisions for their patients.
  
  
  That’s where you come in. We’re offering you a role with purpose. Your contribution at Teckro will lead to faster, safer and more efficient clinical trials. Quality of life will be improved. In the end, lives will be saved.
  
  
  Could you be our newest Teckronaut?
  
  
  Expectations include the ability to build relationships (internally and externally), identify client needs, deliver our strategic and innovative solutions, and ensure that client contracts are delivered on time and on budget. A program lead is responsible for ensuring a superior client experience and driving account growth. This experienced professional exhibits decision quality, action orientation, communication savvy, and resourcefulness to meet both Teckro and client needs. 
   What you’ll Do: 
  
  Ensure the ongoing successful and timely delivery of Teckro products and premium services to clients for the assigned programme/portfolio. Define use cases to support customer business 
  Oversee and ensure the timely and successful delivery of solutions both at implementation and throughout the trial’s lifecycle that align with service level agreements. 
  Establish and manage executive-level relationships with client decision makers and influencers. 
  Develop and manage governance model and issue escalation pathway for assigned client. 
  Establish standards/operating framework that aligns with client needs/expectations to promote standardization and drive efficiency 
  Manage relationships with key existing clients through frequent communication, including formal and informal meetings and client visits. 
  Work with internal teams as well as external stakeholders to identify, monitor and manage risks during the development of the programme and adhere to change control process where applicable. 
  Track, review and assess the implementation and ongoing Teckro KPIs for the programme and identify areas of improvement 
  Working with the client, develop the business case and ROI metrics to demonstrate the value of the Teckro platform across the elements of speed, cost and quality. Ensure access to client data/metrics in order to develop the business case. 
  Regularly contribute ideas for innovation and product, quality, and process improvements 
  Develop long-term relationships with your portfolio of assigned clients, connecting with key business development executives and other stakeholders. 
  Educate clients for assigned programmes on products, new solutions and best practices 
  Ensure that training is provided on Teckro products as needed to clients and new users at a programme level 
  Operate as the lead point of contact for all matters specific to the managed clients for the assigned programme/portfolio/client 
  Proactively identify issues in client service relationships, address these directly and intervene when necessary to ensure client satisfaction. 
  Being an active contributor of the sales team to reach and exceed the sales quota while achieving sales targets. 
  Manage Account Plan development activities for assigned clients and own the development and delivery of the operational delivery plan 
  Participate in conferences and support other Marketing activities to share Teckro’s ROI and use cases for the platform 
  Participate in use case development for Teckro products by phase, stage of development, therapeutic area and study role. 
  Ability and willingness to travel (approximately 20-30%) 
  Undertake other duties in-line with your role and business requirements as required and requested by the hiring manager.
 
  
  The Ideal candidate will have: 
  
  Extensive clinical research and clinical trial experience required, preferably across various a variety of therapeutic areas. Minimum 5 years of clinical research experience. 
  Minimum of 5 years relevant project management experience, preferably in the Lifesciences, Clinical Research and Development space with experience in complex and critical projects 
  Possesses a forward-thinking approach to the management of various internal and external stakeholders. 
  A proven ability to take ownership of projects and achieve required deliverables ensuring projects are delivered to the highest quality. 
  Excellent presentation and communication skills, and ability to demonstrate knowledge of the company products and technology to internal and external stakeholders 
  Highly motivated and organised individual, with particular attention to detail 
  Ability to work on one’s own initiative, whilst also being able to take direction
 
  
  
  Qualifications Required: 
 
  Degree in related field(s); or equivalent combination of relevant work experience and education 
  PM Training – e.g. Applied PM, Commercial PM, or equivalent combination of relevant work experience and education
 
  
  
  Location and Travel: 
  (Dublin/Limerick) 
  
  Hybrid work option with the flexibility to work in our Irish offices located in Dublin or Limerick City. Currently this is set to 3 days per week onsite. 
  We also offer flexible start/ end times, allowing your schedule to suit your lifestyle 
  Willingness to travel internationally as required 
  Please note: Regrettably we cannot offer work permit/sponsorship or self-sponsorship for this role. Eligible applicants must already hold valid and legal work permit for Ireland
 
  
  
  Teckro Benefits:
  
  
  
  25 days holidays 
  Pension 
  Healthcare 
  Life Insurance 
  Share Options 
  50% Maternity leave pay after capped length of service 
  Paid Paternity leave scheme 
  Bike to Work/ Tax Saver Scheme 
  Gym/Wellness Allowance 
  Sports and Social Club
 
  
  
  We are always looking for amazing people to join our growing team. If you are curious, passionate and motivated, then we want to talk to you!
  
  
  By submitting your application, you agree that Teckro may collect your personal data for recruiting and related purposes. Teckro's Recruitment Privacy Statement explains what personal information Teckro may process, where Teckro may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Teckro’s use of your personal information.



Programme Lead - Teckro

Teckro Limited

Programme Lead

You need 8+ years in clinical research and project management, strong stakeholder management, communication skills, attention to detail, and relevant education or equivalent experience.

You will oversee successful delivery of solutions, manage client relationships, track KPIs, ensure training, identify risks, contribute to sales, and participate in marketing activities.

<div>
 About Teckro
 
 
 We founded Teckro to simplify and modernize clinical trials. In fact, thousands of clinical trial investigators and research site staff rely on Teckro to make the most informed decisions for their patients.
 
 
 That’s where you come in. We’re offering you a role with purpose. Your contribution at Teckro will lead to faster, safer and more efficient clinical trials. Quality of life will be improved. In the end, lives will be saved.
 
 
 Could you be our newest Teckronaut?
 
 
 Expectations include the ability to build relationships (internally and externally), identify client needs, deliver our strategic and innovative solutions, and ensure that client contracts are delivered on time and on budget. A program director is responsible for ensuring a superior client experience and driving account growth. 
 This experienced professional exhibits decision quality, action orientation, communication savvy, and resourcefulness to meet both Teckro and client needs. 
 What you’ll Do: 
 <ul> 
 <li>Ensure the ongoing successful and timely delivery of Teckro products and premium services to clients for the assigned programme/portfolio.</li> 
 <li>Oversee and ensure the timely and successful delivery of solutions both at implementation and throughout the trial’s lifecycle that align with service level agreements.</li> 
 <li>Establish and manage executive-level relationships with client decision makers and influencers.</li> 
 <li>Develop and manage governance model and issue escalation pathway for assigned client. Establish standards/operating framework that aligns with client needs/expectations</li> 
 <li>Manage relationships with key existing clients through frequent communication, including formal and informal meetings and client visits.</li> 
 <li>Work with internal teams as well as external stakeholders to identify, monitor and manage risks during the development of the programme and adhere to change control process where applicable. </li>
 <li>Track, review and assess the implementation and ongoing Teckro KPIs for the programme and identify areas of improvement </li>
 <li>Working with the client, develop the business case and ROI metrics to demonstrate the value of the Teckro platform across the elements of speed, cost and quality. Ensure access to client data/metrics in order to develop the business case.</li> 
 <li>Ensure sponsor/programme specific KPIs and requirements are met/delivered consistently by the Professional Services team assigned to the programme</li> 
 <li>Regularly contribute ideas for innovation and product, quality, and process improvements </li>
 <li>Develop long-term relationships with your portfolio of assigned clients, connecting with key business development executives and other stakeholders.</li> 
 <li>Educate clients for assigned programmes on products, new solutions and best practices</li> 
 <li>Ensure that training is provided on Teckro products as needed to clients and new users at a programme level</li> 
 <li>Operate as the lead point of contact for all matters specific to the managed clients for the assigned programme/portfolio/client</li> 
 <li>Proactively identify issues in client service relationships, address these directly and intervene when necessary to ensure client satisfaction.</li> 
 <li>Being an active contributor of the sales team to reach and exceed the sales quota while achieving sales targets. </li>
 <li>Manage Account Plan development activities for assigned clients and own the development and delivery of the operational delivery plan</li> 
 <li>Participate in conferences and support other Marketing activities to share Teckro’s ROI and use cases for the platform</li> 
 <li>Participate in use case development for Teckro products by phase, stage of development, therapeutic area and study role.</li> 
 <li>Ability and willingness to travel (approximately 20-30%) </li>
 <li>Undertake other duties in-line with your role and business requirements as required and requested by the hiring manager.</li>
 </ul>
 
 
 The Ideal candidate will have: 
 <ul> 
 <li>Extensive clinical research and clinical trial experience required, preferably across various a variety of therapeutic areas. Minimum of 8 years of clinical research experience.</li> 
 <li>Minimum of 8 years relevant project management experience, preferably in the Lifesciences, Clinical Research and Development space with experience in complex and critical projects</li> 
 <li>Possesses a forward-thinking approach to the management of various internal and external stakeholders. </li>
 <li>A proven ability to take ownership of projects and achieve required deliverables ensuring projects are delivered to the highest quality.</li> 
 <li>Excellent presentation and communication skills, and ability to demonstrate knowledge of the company products and technology to internal and external stakeholders</li> 
 <li>Highly motivated and organised individual, with particular attention to detail</li> 
 <li>Ability to work on one’s own initiative, whilst also being able to take direction</li>
 </ul>
 
 
 Qualifications Required: 
 <ul>
 <li>Degree in related field(s); or equivalent combination of relevant work experience and education</li> 
 <li>PM Training – e.g. Applied PM, Commercial PM, or equivalent combination of relevant work experience and education</li>
 </ul>
 
 
 Location and Travel: 
 (Dublin/Limerick) 
 <ul> 
 <li>Hybrid work option with the flexibility to work in our Irish offices located in Dublin or Limerick City. Currently this is set to 3 days per week onsite.</li> 
 <li>We also offer flexible start/ end times, allowing your schedule to suit your lifestyle</li> 
 <li>Willingness to travel internationally as required</li> 
 <li>Please note: Regrettably we cannot offer work permit/sponsorship or self-sponsorship for this role. Eligible applicants must already hold valid and legal work permit for Ireland</li>
 </ul>
 
 
 Teckro Benefits:
 
 
 <ul> 
 <li>25 days holidays</li> 
 <li>Pension</li> 
 <li>Healthcare</li> 
 <li>Life Insurance</li> 
 <li>Share Options</li> 
 <li>50% Maternity leave pay after capped length of service</li> 
 <li>Paid Paternity leave scheme</li> 
 <li>Bike to Work/ Tax Saver Scheme</li> 
 <li>Gym/Wellness Allowance</li> 
 <li>Sports and Social Club</li>
 </ul>
 
 We are always looking for amazing people to join our growing team. If you are curious, passionate and motivated, then we want to talk to you!
 
 
 By submitting your application, you agree that Teckro may collect your personal data for recruiting and related purposes. Teckro's Recruitment Privacy Statement explains what personal information Teckro may process, where Teckro may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Teckro’s use of your personal information.
</div>


 About Teckro
  
  
  We founded Teckro to simplify and modernize clinical trials. In fact, thousands of clinical trial investigators and research site staff rely on Teckro to make the most informed decisions for their patients.
  
  
  That’s where you come in. We’re offering you a role with purpose. Your contribution at Teckro will lead to faster, safer and more efficient clinical trials. Quality of life will be improved. In the end, lives will be saved.
  
  
  Could you be our newest Teckronaut?
  
  
  Expectations include the ability to build relationships (internally and externally), identify client needs, deliver our strategic and innovative solutions, and ensure that client contracts are delivered on time and on budget. A program director is responsible for ensuring a superior client experience and driving account growth. 
  This experienced professional exhibits decision quality, action orientation, communication savvy, and resourcefulness to meet both Teckro and client needs. 
   What you’ll Do: 
  
  Ensure the ongoing successful and timely delivery of Teckro products and premium services to clients for the assigned programme/portfolio. 
  Oversee and ensure the timely and successful delivery of solutions both at implementation and throughout the trial’s lifecycle that align with service level agreements. 
  Establish and manage executive-level relationships with client decision makers and influencers. 
  Develop and manage governance model and issue escalation pathway for assigned client. Establish standards/operating framework that aligns with client needs/expectations 
  Manage relationships with key existing clients through frequent communication, including formal and informal meetings and client visits. 
  Work with internal teams as well as external stakeholders to identify, monitor and manage risks during the development of the programme and adhere to change control process where applicable. 
  Track, review and assess the implementation and ongoing Teckro KPIs for the programme and identify areas of improvement 
  Working with the client, develop the business case and ROI metrics to demonstrate the value of the Teckro platform across the elements of speed, cost and quality. Ensure access to client data/metrics in order to develop the business case. 
  Ensure sponsor/programme specific KPIs and requirements are met/delivered consistently by the Professional Services team assigned to the programme 
  Regularly contribute ideas for innovation and product, quality, and process improvements 
  Develop long-term relationships with your portfolio of assigned clients, connecting with key business development executives and other stakeholders. 
  Educate clients for assigned programmes on products, new solutions and best practices 
  Ensure that training is provided on Teckro products as needed to clients and new users at a programme level 
  Operate as the lead point of contact for all matters specific to the managed clients for the assigned programme/portfolio/client 
  Proactively identify issues in client service relationships, address these directly and intervene when necessary to ensure client satisfaction. 
  Being an active contributor of the sales team to reach and exceed the sales quota while achieving sales targets. 
  Manage Account Plan development activities for assigned clients and own the development and delivery of the operational delivery plan 
  Participate in conferences and support other Marketing activities to share Teckro’s ROI and use cases for the platform 
  Participate in use case development for Teckro products by phase, stage of development, therapeutic area and study role. 
  Ability and willingness to travel (approximately 20-30%) 
  Undertake other duties in-line with your role and business requirements as required and requested by the hiring manager.
 
  
  
  The Ideal candidate will have: 
  
  Extensive clinical research and clinical trial experience required, preferably across various a variety of therapeutic areas. Minimum of 8 years of clinical research experience. 
  Minimum of 8 years relevant project management experience, preferably in the Lifesciences, Clinical Research and Development space with experience in complex and critical projects 
  Possesses a forward-thinking approach to the management of various internal and external stakeholders. 
  A proven ability to take ownership of projects and achieve required deliverables ensuring projects are delivered to the highest quality. 
  Excellent presentation and communication skills, and ability to demonstrate knowledge of the company products and technology to internal and external stakeholders 
  Highly motivated and organised individual, with particular attention to detail 
  Ability to work on one’s own initiative, whilst also being able to take direction
 
  
  
  Qualifications Required: 
 
  Degree in related field(s); or equivalent combination of relevant work experience and education 
  PM Training – e.g. Applied PM, Commercial PM, or equivalent combination of relevant work experience and education
 
  
  
  Location and Travel: 
  (Dublin/Limerick) 
  
  Hybrid work option with the flexibility to work in our Irish offices located in Dublin or Limerick City. Currently this is set to 3 days per week onsite. 
  We also offer flexible start/ end times, allowing your schedule to suit your lifestyle 
  Willingness to travel internationally as required 
  Please note: Regrettably we cannot offer work permit/sponsorship or self-sponsorship for this role. Eligible applicants must already hold valid and legal work permit for Ireland
 
  
  
  Teckro Benefits:
  
  
  
  25 days holidays 
  Pension 
  Healthcare 
  Life Insurance 
  Share Options 
  50% Maternity leave pay after capped length of service 
  Paid Paternity leave scheme 
  Bike to Work/ Tax Saver Scheme 
  Gym/Wellness Allowance 
  Sports and Social Club
 
 
  We are always looking for amazing people to join our growing team. If you are curious, passionate and motivated, then we want to talk to you!
  
  
  By submitting your application, you agree that Teckro may collect your personal data for recruiting and related purposes. Teckro's Recruitment Privacy Statement explains what personal information Teckro may process, where Teckro may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Teckro’s use of your personal information.



Programme Director - Teckro

Programme Director

You must be a fluent Chinese speaker with 3+ years in clinical research, strong critical thinking, and tech-savvy. Hold a relevant degree; postgraduate qualification preferred.

You will advise on clinical trials, review protocols, analyze risks, present findings, mentor junior members, assist in training, provide feedback on the platform, and contribute to process improvements.

<div>
 About Teckro
 
 We founded Teckro to simplify and modernize clinical trials. In fact, thousands of clinical trial investigators and research site staff rely on Teckro to make the most informed decisions for their patients.
 
 That’s where you come in. We’re offering you a role with purpose. Your contribution at Teckro will lead to faster, safer and more efficient clinical trials. Quality of life will be improved. In the end, lives will be saved.
 
 Could you be our newest Teckronaut? 
 
 Expectations include the ability to build relationships (internally and externally), identify client needs, deliver our strategic and innovative solutions, and ensure that client contracts are delivered on time and on budget. A program director is responsible for ensuring a superior client experience and driving account growth.
 This experienced professional exhibits decision quality, action orientation, communication savvy, and resourcefulness to meet both Teckro and client needs.
 
 What you’ll Do:
 <ul>
 <li>Act as a clinical trial advisor and subject matter expert, providing clinical oversight on a multidisciplinary team, to ensure timely delivery of high quality solutions</li>
 <li>Review study protocols/documents to identify areas of vulnerability and operational importance; customizing the platform to meet the requirements of individual studies</li>
 <li>Review projects from an End Users perspective to ensure quality, accuracy and relevance before being deployed to the client</li>
 <li>Review/analyze program/study-level risk registers/RACTs to assist in defining messaging campaigns or other use cases for the Teckro platform in order to help client study teams meet study objectives and minimize study risks.</li>
 <li>Present findings/suggestions to client study teams with support from Project Manager and/or Program Lead/Director for assigned account</li>
 <li>Monitoring/analyzing of platform searches: identification of trends and unanticipated key variables; providing data to the development teams for product improvements.</li>
 <li>Act as a clinical trials resource for the Product team: assisting with testing new functions and providing insight into the day to day work of a clinical research professional.</li>
 <li>Contribute to maintaining and improving in-house templates, SOPs and guides.</li>
 <li>Where required, assist in the Induction, training and upskilling of junior team members, mentoring and providing insight into Clinical Trial Operations.</li>
 <li>Undertake other duties in-line with your role and business requirements as required</li>
 <li>Regularly contribute ideas for innovation and product, quality and process improvements and additions</li>
 </ul> 
 
 Multilingual CRS:
 <ul>
 <li>Assist with translation tasks across various departments within the company</li>
 <li>To perform study demos of Teckro, to join Investigator’s Meetings (IMs) and to provide training in local languages to study teams and/or relevant users</li>
 </ul> 
 
 The Ideal candidate will have:
 <ul>
 <li>Chinese speaker, with the ability to communicate fluently; including reading, writing, listening and speaking.</li>
 <li>In dept knowledge of global drug development, clinical trial processes, ICH-GCP, regulations and documentation</li>
 <li>Minimum 3 years of clinical operations/clinical research experience within a hospital or CRO setting (study coordinator, research nurse, CRA/study monitor) or if applicable, have completed and successfully passed ‘In-House Clinical Trial Training programme’ and have proven competencies from CRS Level 3.</li>
 <li>Broad clinical research experience from working within a variety of therapeuticises preferred.</li>
 <li>Keen interest in technology solutions and Software as a Service (SaaS)</li>
 <li>Experience with clinical operations/industry-related technology solutions and a keen ability to learn new software preferred.</li>
 <li>Strong critical thinking and problem solving skills</li>
 <li>Strong multi-tasking and time management skills including the ability to effectively prioritise tasks, depending on timelines and demands</li>
 <li>Ability to work both independently and in a team-orientated, collaborative environment – able to get the work done, with minimal or no supervision</li>
 <li>Strong interpersonal, verbal and written communication skills</li>
 <li>Results and performance driven</li>
 <li>Adaptable and flexible</li>
 </ul> 
 
 Qualifications Required:
 <ul>
 <li>Degree in biological science, nursing, or other health-related discipline.</li>
 <li>Post graduate qualification in Clinical Research preferred.</li>
 <li>Proven competencies with Clinical Research methodologies and operational day to day activities.</li>
 </ul>
 
 Location and Travel:
 (Dublin/Limerick)
 <ul>
 <li>Hybrid work option with the flexibility to work in our Irish offices located in Dublin or Limerick City. Currently this is set to 3 days per week onsite.</li>
 <li>We also offer flexible start/ end times, allowing your schedule to suit your lifestyle</li>
 <li>Willingness to travel internationally as required</li>
 <li>Please note: Regrettably we cannot offer work permit/sponsorship or self-sponsorship for this role. Eligible applicants must already hold valid and legal work permit for Ireland</li>
 </ul> 
 
 Teckro Benefits: 
 
 <ul>
 <li>25 days holidays</li>
 <li>Pension</li>
 <li>Healthcare</li>
 <li>Life Insurance</li>
 <li>Share Options</li>
 <li>50% Maternity leave pay after capped length of service</li>
 <li>Paid Paternity leave scheme</li>
 <li>Bike to Work/ Tax Saver Scheme</li>
 <li>Gym/Wellness Allowance</li>
 <li>Sports and Social Club</li>
 </ul> 
 
 We are always looking for amazing people to join our growing team. If you are curious, passionate and motivated, then we want to talk to you!
 
 By submitting your application, you agree that Teckro may collect your personal data for recruiting and related purposes. Teckro's Recruitment Privacy Statement explains what personal information Teckro may process, where Teckro may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Teckro’s use of your personal information.
</div>


 About Teckro
 
  We founded Teckro to simplify and modernize clinical trials. In fact, thousands of clinical trial investigators and research site staff rely on Teckro to make the most informed decisions for their patients.
 
  That’s where you come in. We’re offering you a role with purpose. Your contribution at Teckro will lead to faster, safer and more efficient clinical trials. Quality of life will be improved. In the end, lives will be saved.
 
  Could you be our newest Teckronaut?
 
 Expectations include the ability to build relationships (internally and externally), identify client needs, deliver our strategic and innovative solutions, and ensure that client contracts are delivered on time and on budget. A program director is responsible for ensuring a superior client experience and driving account growth.
 This experienced professional exhibits decision quality, action orientation, communication savvy, and resourcefulness to meet both Teckro and client needs.
 
  What you’ll Do:
 
  Act as a clinical trial advisor and subject matter expert, providing clinical oversight on a multidisciplinary team, to ensure timely delivery of high quality solutions
  Review study protocols/documents to identify areas of vulnerability and operational importance; customizing the platform to meet the requirements of individual studies
  Review projects from an End Users perspective to ensure quality, accuracy and relevance before being deployed to the client
  Review/analyze program/study-level risk registers/RACTs to assist in defining messaging campaigns or other use cases for the Teckro platform in order to help client study teams meet study objectives and minimize study risks.
  Present findings/suggestions to client study teams with support from Project Manager and/or Program Lead/Director for assigned account
  Monitoring/analyzing of platform searches: identification of trends and unanticipated key variables; providing data to the development teams for product improvements.
  Act as a clinical trials resource for the Product team: assisting with testing new functions and providing insight into the day to day work of a clinical research professional.
  Contribute to maintaining and improving in-house templates, SOPs and guides.
  Where required, assist in the Induction, training and upskilling of junior team members, mentoring and providing insight into Clinical Trial Operations.
  Undertake other duties in-line with your role and business requirements as required
  Regularly contribute ideas for innovation and product, quality and process improvements and additions
 
 
  Multilingual CRS:
 
  Assist with translation tasks across various departments within the company
  To perform study demos of Teckro, to join Investigator’s Meetings (IMs) and to provide training in local languages to study teams and/or relevant users
 
 
  The Ideal candidate will have:
 
  Chinese speaker, with the ability to communicate fluently; including reading, writing, listening and speaking.
  In dept knowledge of global drug development, clinical trial processes, ICH-GCP, regulations and documentation
  Minimum 3 years of clinical operations/clinical research experience within a hospital or CRO setting (study coordinator, research nurse, CRA/study monitor) or if applicable, have completed and successfully passed ‘In-House Clinical Trial Training programme’ and have proven competencies from CRS Level 3.
  Broad clinical research experience from working within a variety of therapeuticises preferred.
  Keen interest in technology solutions and Software as a Service (SaaS)
  Experience with clinical operations/industry-related technology solutions and a keen ability to learn new software preferred.
  Strong critical thinking and problem solving skills
  Strong multi-tasking and time management skills including the ability to effectively prioritise tasks, depending on timelines and demands
  Ability to work both independently and in a team-orientated, collaborative environment – able to get the work done, with minimal or no supervision
  Strong interpersonal, verbal and written communication skills
  Results and performance driven
  Adaptable and flexible
 
 
  Qualifications Required:
 
  Degree in biological science, nursing, or other health-related discipline.
  Post graduate qualification in Clinical Research preferred.
  Proven competencies with Clinical Research methodologies and operational day to day activities.
 
 
  Location and Travel:
 (Dublin/Limerick)
 
  Hybrid work option with the flexibility to work in our Irish offices located in Dublin or Limerick City. Currently this is set to 3 days per week onsite.
  We also offer flexible start/ end times, allowing your schedule to suit your lifestyle
  Willingness to travel internationally as required
  Please note: Regrettably we cannot offer work permit/sponsorship or self-sponsorship for this role. Eligible applicants must already hold valid and legal work permit for Ireland
 
 
  Teckro Benefits:
 
 
  25 days holidays
  Pension
  Healthcare
  Life Insurance
  Share Options
  50% Maternity leave pay after capped length of service
  Paid Paternity leave scheme
  Bike to Work/ Tax Saver Scheme
  Gym/Wellness Allowance
  Sports and Social Club
 
 
 We are always looking for amazing people to join our growing team. If you are curious, passionate and motivated, then we want to talk to you!
 
  By submitting your application, you agree that Teckro may collect your personal data for recruiting and related purposes. Teckro's Recruitment Privacy Statement explains what personal information Teckro may process, where Teckro may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Teckro’s use of your personal information.



Senior Clinical Research Specialist - Chinese Speaking - Teckro

Senior Clinical Research Specialist - Chinese Speaking

You should have a degree in a health-related field, strong communication skills, critical thinking, adaptability, and a keen interest in clinical research. Excellent computer skills are essential.

You will analyze complex scientific information, collaborate with teams for solutions, structure clinical data, monitor user feedback, and perform additional duties as needed.

<div>
 About Teckro 
 
 We founded Teckro to simplify and modernize clinical trials. In fact, thousands of clinical trial investigators and research site staff rely on Teckro to make the most informed decisions for their patients. 
 
 That’s where you come in. We’re offering you a role with purpose. Your contribution at Teckro will lead to faster, safer and more efficient clinical trials. Quality of life will be improved. In the end, lives will be saved. 
 
 Could you be our newest Teckronaut? 
 
 Expectations include the ability to build relationships (internally and externally), identify client needs, deliver our strategic and innovative solutions, and ensure that client contracts are delivered on time and on budget. A program director is responsible for ensuring a superior client experience and driving account growth.
 This experienced professional exhibits decision quality, action orientation, communication savvy, and resourcefulness to meet both Teckro and client needs.
 
 What you’ll Do:
 <ul>
 <li>Analyse, understand, and process complex scientific/medical/pharmaceutical information</li>
 <li>Work with study teams and internal project teams to ensure timely delivery of high-quality solutions</li>
 <li>Execute the layout and structure of clinical information required to utilize our products efficiently and effectively</li>
 <li>Monitor, analyse, and action end user feedback and usage analysis metrics to evaluate and improve usability and accuracy of our products</li>
 <li>Undertake other duties in-line with your role expertise and business requirements as required</li>
 </ul> 
 
 The Ideal candidate will have:
 <ul>
 <li>Genuine interest in clinical research, medical advancement and drug and biotechnology development highly beneficial as there is room for advancement within the Clinical Trials area in Teckro</li>
 <li>Superb editorial skills with a keen eye for text and graphic layouts</li>
 <li>Strong critical thinking and problem solving skills</li>
 <li>Strong multi-tasking and time management skills including the ability to effectively prioritise tasks, depending on timelines and demands</li>
 <li>Strong interpersonal, verbal and written communication skills</li>
 <li>Proven ability to organize information in a logical and systematic way</li>
 <li>Ability to focus on fine details and the wider system at the same time</li>
 <li>Highly adaptable and flexible</li>
 <li>Ability to quickly and easily switch contexts, particularly between creative and analytical work</li>
 <li>Passion for creative solutions, innovation, and divergent thinking</li>
 <li>Demonstrated ability to work well as part of a team</li>
 <li>Where a candidate is carry out duties in a specific language, proven spoken and written fluency is essential</li>
 </ul> 
 
 Qualifications Required:
 <ul>
 <li>Degree in biological science, nursing, pharmacology, other health-related field or prior qualifications or experience in technical communications preferred</li>
 <li>Genuine interest in clinical research, medical advancement and drug and biotechnology development highly beneficial as there is room for advancement within the Clinical Trials area in Teckro.</li>
 <li>Excellent computer skills</li>
 </ul>
 Location and Travel:
 (Dublin/Limerick)
 <ul>
 <li>Hybrid work option with the flexibility to work in our Irish offices located in Dublin or Limerick City. Currently this is set to 3 days per week onsite.</li>
 <li>We also offer flexible start/ end times, allowing your schedule to suit your lifestyle</li>
 <li>Willingness to travel internationally as required</li>
 <li>Please note: Regrettably we cannot offer work permit/sponsorship or self-sponsorship for this role. Eligible applicants must already hold valid and legal work permit for Ireland</li>
 </ul> 
 
 Teckro Benefits: 
 
 <ul>
 <li>25 days holidays</li>
 <li>Pension</li>
 <li>Healthcare</li>
 <li>Life Insurance</li>
 <li>Share Options</li>
 <li>50% Maternity leave pay after capped length of service</li>
 <li>Paid Paternity leave scheme</li>
 <li>Bike to Work/ Tax Saver Scheme</li>
 <li>Gym/Wellness Allowance</li>
 <li>Sports and Social Club</li>
 </ul> 
 
 We are always looking for amazing people to join our growing team. If you are curious, passionate and motivated, then we want to talk to you! 
 
 By submitting your application, you agree that Teckro may collect your personal data for recruiting and related purposes. Teckro's Recruitment Privacy Statement explains what personal information Teckro may process, where Teckro may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Teckro’s use of your personal information.
</div>


 About Teckro
 
 We founded Teckro to simplify and modernize clinical trials. In fact, thousands of clinical trial investigators and research site staff rely on Teckro to make the most informed decisions for their patients.
 
 That’s where you come in. We’re offering you a role with purpose. Your contribution at Teckro will lead to faster, safer and more efficient clinical trials. Quality of life will be improved. In the end, lives will be saved.
 
 Could you be our newest Teckronaut?
 
 Expectations include the ability to build relationships (internally and externally), identify client needs, deliver our strategic and innovative solutions, and ensure that client contracts are delivered on time and on budget. A program director is responsible for ensuring a superior client experience and driving account growth.
 This experienced professional exhibits decision quality, action orientation, communication savvy, and resourcefulness to meet both Teckro and client needs.
 
  What you’ll Do:
 
  Analyse, understand, and process complex scientific/medical/pharmaceutical information
  Work with study teams and internal project teams to ensure timely delivery of high-quality solutions
  Execute the layout and structure of clinical information required to utilize our products efficiently and effectively
  Monitor, analyse, and action end user feedback and usage analysis metrics to evaluate and improve usability and accuracy of our products
  Undertake other duties in-line with your role expertise and business requirements as required
 
 
  The Ideal candidate will have:
 
  Genuine interest in clinical research, medical advancement and drug and biotechnology development highly beneficial as there is room for advancement within the Clinical Trials area in Teckro
  Superb editorial skills with a keen eye for text and graphic layouts
  Strong critical thinking and problem solving skills
  Strong multi-tasking and time management skills including the ability to effectively prioritise tasks, depending on timelines and demands
  Strong interpersonal, verbal and written communication skills
  Proven ability to organize information in a logical and systematic way
  Ability to focus on fine details and the wider system at the same time
  Highly adaptable and flexible
  Ability to quickly and easily switch contexts, particularly between creative and analytical work
  Passion for creative solutions, innovation, and divergent thinking
  Demonstrated ability to work well as part of a team
  Where a candidate is carry out duties in a specific language, proven spoken and written fluency is essential
 
 
  Qualifications Required:
 
  Degree in biological science, nursing, pharmacology, other health-related field or prior qualifications or experience in technical communications preferred
  Genuine interest in clinical research, medical advancement and drug and biotechnology development highly beneficial as there is room for advancement within the Clinical Trials area in Teckro.
  Excellent computer skills
 
 Location and Travel:
 (Dublin/Limerick)
 
  Hybrid work option with the flexibility to work in our Irish offices located in Dublin or Limerick City. Currently this is set to 3 days per week onsite.
  We also offer flexible start/ end times, allowing your schedule to suit your lifestyle
  Willingness to travel internationally as required
  Please note: Regrettably we cannot offer work permit/sponsorship or self-sponsorship for this role. Eligible applicants must already hold valid and legal work permit for Ireland
 
 
  Teckro Benefits:
 
 
  25 days holidays
  Pension
  Healthcare
  Life Insurance
  Share Options
  50% Maternity leave pay after capped length of service
  Paid Paternity leave scheme
  Bike to Work/ Tax Saver Scheme
  Gym/Wellness Allowance
  Sports and Social Club
 
 
 We are always looking for amazing people to join our growing team. If you are curious, passionate and motivated, then we want to talk to you!
 
 By submitting your application, you agree that Teckro may collect your personal data for recruiting and related purposes. Teckro's Recruitment Privacy Statement explains what personal information Teckro may process, where Teckro may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Teckro’s use of your personal information.



Clinical Research Specialist (Entry Level) - Teckro

Clinical Research Specialist (Entry Level)

You need 5+ years in healthcare project or account management, 3+ years in clinical trial management, strong client relations, organizational skills, and a BA/BS degree; international travel may be required.

You will manage client relationships, ensure product delivery, identify issues, educate clients, support sales, mentor team members, and collaborate across departments while traveling as needed.

Customer Relations

<div>
 About Teckro 
 
 We founded Teckro to simplify and modernize clinical trials. In fact, thousands of clinical trial investigators and research site staff rely on Teckro to make the most informed decisions for their patients. 
 
 That’s where you come in. We’re offering you a role with purpose. Your contribution at Teckro will lead to faster, safer and more efficient clinical trials. Quality of life will be improved. In the end, lives will be saved. 
 
 Could you be our newest Teckronaut?
 
 What you’ll Do:
 <ul>
 <li>Ensure the ongoing successful delivery of Teckro products to clients by building strong and productive relationships with clients and co-workers.</li>
 <li>As lead point of contact for key existing clients, manage day to day relationships with these teams to ensure ongoing client satisfaction through frequent communication, meetings and client visits.</li>
 <li>Develop long-term relationships with clients to help grow these accounts within Teckro by connecting with key business executives and stakeholders.</li>
 <li>Proactively identify potential and existing issues in client service relationships, address these directly and intervene when necessary to ensure client satisfaction. Recommend Teckro solutions to help solve these where possible.</li>
 <li>Develop site engagement strategies with the clinical study team using Teckro solutions, data and communication channels.</li>
 <li>Leverage Teckro data and metrics for clients with the objective of adding value to the clinical trial or programme.</li>
 <li>Responsible for educating clients on products, new solutions and best practices.</li>
 <li>Ensure the timely and successful delivery of our solutions according to customer needs and objectives.</li>
 <li>Provide support to Head of Clinical Engagement and/or Senior Management in the areas of engagement/growth strategy, process and reporting.</li>
 <li>Be an active contributor to the sales team to reach and exceed the sales quota while achieving sales targets.</li>
 <li>Provide training and mentoring support to assigned members of the Engagement Project Management team.</li>
 <li>Contribute to the Engagement Project Management team process creation and process improvement.</li>
 <li>Ensure successful collaboration of the Engagement PM team with other departments, as required.</li>
 <li>Ability to travel (approximately 20-30%)</li>
 <li>Undertake other duties in-line with your role and business needs as required.</li>
 </ul> 
 The Ideal candidate will have: 
 
 <ul>
 <li>5+ years of healthcare project management, account management and/or clinical research experience.</li>
 <li>3+ years’ experience in clinical trial management or similar.</li>
 <li>Experience in delivering client-focused solutions based on customer needs.</li>
 <li>Proven ability to manage multiple projects at a time while paying strict attention to detail.</li>
 <li>Ability to form strong and constructive internal as well as external professional relationships.</li>
 <li>Demonstrated ability to shape, and deliver results to, customer expectations.</li>
 <li>Strong influencing, negotiation skills and presentation skills.</li>
 <li>Excellent communication, interpersonal, organizational and telephone skills.</li>
 </ul> 
 
 Qualifications Required: 
 
 <ul>
 <li>BA/BS degree in related field; or equivalent combination of relevant work experience and education.</li>
 </ul> 
 
 Location and Travel: 
 (Dublin/Limerick)
 <ul>
 <li>Hybrid work option with the flexibility to work in our Irish offices located in Dublin or Limerick City. Currently this is set to 3 days per week onsite.</li>
 <li>We also offer flexible start/ end times, allowing your schedule to suit your lifestyle</li>
 <li>Willingness to travel internationally as required</li>
 <li>Please note: Regrettably we cannot offer work permit/sponsorship or self-sponsorship for this role. Eligible applicants must already hold valid and legal work permit for Ireland</li>
 </ul> 
 
 Teckro Benefits: 
 
 <ul>
 <li>25 days holidays</li>
 <li>Pension</li>
 <li>Healthcare</li>
 <li>Life Insurance</li>
 <li>Share Options</li>
 <li>50% Maternity leave pay after capped length of service</li>
 <li>Paid Paternity leave scheme</li>
 <li>Bike to Work/ Tax Saver Scheme</li>
 <li>Gym/Wellness Allowance</li>
 <li>Sports and Social Club</li>
 </ul>
 
 We are always looking for amazing people to join our growing team. If you are curious, passionate and motivated, then we want to talk to you! 
 
 By submitting your application, you agree that Teckro may collect your personal data for recruiting and related purposes. Teckro's Recruitment Privacy Statement explains what personal information Teckro may process, where Teckro may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Teckro’s use of your personal information.
</div>


 About Teckro
 
 We founded Teckro to simplify and modernize clinical trials. In fact, thousands of clinical trial investigators and research site staff rely on Teckro to make the most informed decisions for their patients.
 
 That’s where you come in. We’re offering you a role with purpose. Your contribution at Teckro will lead to faster, safer and more efficient clinical trials. Quality of life will be improved. In the end, lives will be saved.
 
 Could you be our newest Teckronaut?
 
  What you’ll Do:
 
  Ensure the ongoing successful delivery of Teckro products to clients by building strong and productive relationships with clients and co-workers.
  As lead point of contact for key existing clients, manage day to day relationships with these teams to ensure ongoing client satisfaction through frequent communication, meetings and client visits.
  Develop long-term relationships with clients to help grow these accounts within Teckro by connecting with key business executives and stakeholders.
  Proactively identify potential and existing issues in client service relationships, address these directly and intervene when necessary to ensure client satisfaction. Recommend Teckro solutions to help solve these where possible.
  Develop site engagement strategies with the clinical study team using Teckro solutions, data and communication channels.
  Leverage Teckro data and metrics for clients with the objective of adding value to the clinical trial or programme.
  Responsible for educating clients on products, new solutions and best practices.
  Ensure the timely and successful delivery of our solutions according to customer needs and objectives.
  Provide support to Head of Clinical Engagement and/or Senior Management in the areas of engagement/growth strategy, process and reporting.
  Be an active contributor to the sales team to reach and exceed the sales quota while achieving sales targets.
  Provide training and mentoring support to assigned members of the Engagement Project Management team.
  Contribute to the Engagement Project Management team process creation and process improvement.
  Ensure successful collaboration of the Engagement PM team with other departments, as required.
  Ability to travel (approximately 20-30%)
  Undertake other duties in-line with your role and business needs as required.
 
  The Ideal candidate will have: 
 
 
  5+ years of healthcare project management, account management and/or clinical research experience.
  3+ years’ experience in clinical trial management or similar.
  Experience in delivering client-focused solutions based on customer needs.
  Proven ability to manage multiple projects at a time while paying strict attention to detail.
  Ability to form strong and constructive internal as well as external professional relationships.
  Demonstrated ability to shape, and deliver results to, customer expectations.
  Strong influencing, negotiation skills and presentation skills.
  Excellent communication, interpersonal, organizational and telephone skills.
 
 
  Qualifications Required: 
 
 
  BA/BS degree in related field; or equivalent combination of relevant work experience and education.
 
 
  Location and Travel:  
 (Dublin/Limerick)
 
  Hybrid work option with the flexibility to work in our Irish offices located in Dublin or Limerick City. Currently this is set to 3 days per week onsite.
  We also offer flexible start/ end times, allowing your schedule to suit your lifestyle
  Willingness to travel internationally as required
  Please note: Regrettably we cannot offer work permit/sponsorship or self-sponsorship for this role. Eligible applicants must already hold valid and legal work permit for Ireland
 
 
  Teckro Benefits:
 
 
  25 days holidays
  Pension
  Healthcare
  Life Insurance
  Share Options
  50% Maternity leave pay after capped length of service
  Paid Paternity leave scheme
  Bike to Work/ Tax Saver Scheme
  Gym/Wellness Allowance
  Sports and Social Club
 
 
  We are always looking for amazing people to join our growing team. If you are curious, passionate and motivated, then we want to talk to you!
 
 By submitting your application, you agree that Teckro may collect your personal data for recruiting and related purposes. Teckro's Recruitment Privacy Statement explains what personal information Teckro may process, where Teckro may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Teckro’s use of your personal information.



Teckro

navigation.mission