Senior Clinical Research Specialist - Chinese Speaking

Teckro

Sep 6

Applications are closed

Job
Full-time
Mid Level
Dublin

Requirements

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.

Responsibilities

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
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

FAQs

What is the primary purpose of the Senior Clinical Research Specialist role at Teckro?

The primary purpose of this role is to simplify and modernize clinical trials, leading to faster, safer, and more efficient clinical trials, ultimately improving quality of life and saving lives.

Is Chinese language proficiency a requirement for this position?

Yes, fluency in Chinese, including reading, writing, listening, and speaking, is a requirement for this role.

What is the required experience for applicants?

Applicants should have a minimum of 3 years of clinical operations/clinical research experience within a hospital or CRO setting or have completed an ‘In-House Clinical Trial Training programme’ with proven competencies from CRS Level 3.

What type of educational background is preferred for this position?

A degree in biological science, nursing, or another health-related discipline is required, and a postgraduate qualification in Clinical Research is preferred.

Where is the role located?

The role can be based in either Dublin or Limerick City in Ireland.

What is the hybrid work policy?

The hybrid work policy allows for flexibility to work both at home and on-site, with currently set expectations of 3 days per week onsite.

Are there opportunities for mentoring in this role?

Yes, the Senior Clinical Research Specialist will assist in the induction, training, and upskilling of junior team members while providing mentorship and insight into Clinical Trial Operations.

What benefits does Teckro offer to its employees?

Teckro offers 25 days of holidays, pension, healthcare, life insurance, share options, maternity and paternity leave schemes, a bike-to-work scheme, gym/wellness allowance, and a sports and social club.

Is international travel a requirement for this position?

Yes, there is a willingness to travel internationally as required for the role.

Does Teckro support work permit sponsorship for this role?

No, Teckro does not support work permit/sponsorship; eligible applicants must already hold a valid and legal work permit for Ireland.

Teckro

Redefining Site Engagement

Technology

Industry

51-200

Employees

2015

Founded Year

Mission & Purpose

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.