Flexible Work Environment

State-of-the-Art Offices

Workplace Journey

Training and Development

All the Perks

Health Insurance

Health Savings Account (HSA)

Vision Insurance

Disability Insurance

Mental Health Care

Supplemental Life Insurance

Dental Insurance

Large

People

Community

Compliance

Medpace is a UK-based clinical research organisation (CRO) that specializes in providing comprehensive and tailored services to pharmaceutical and biotechnology companies. Their ultimate mission is to accelerate the development of life-saving and life-improving therapies through high-quality and efficient clinical trials. Medpace's purpose is to collaborate with their clients to bring innovative medical treatments to market by offering expertise in study design, regulatory support, site management, and data analysis. They aim to advance medical knowledge and improve patient outcomes while upholding the highest ethical and scientific standards in clinical research within the UK and globally.

Science & Healthcare

Medpace

Pharmaceuticals

Accelerating Drug, Biologic and Medical Device Clinical Development

You need a Bachelor's in a healthcare field, clinical or pharmacovigilance experience, English proficiency, Microsoft Office skills, medical terminology knowledge, and strong organizational and communication skills.

You will manage incoming calls, track adverse events, write safety narratives, report safety data, and collaborate with departments and research sites to ensure compliance.

Research & Development

Healthcare

We are currently seeking a full-time, office-based Clinical Safety Coordinator to join our Clinical Safety department in India. This position will be focused on the handling and processing of adverse events from all sources, including clinical trials and post marketing surveillance. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you! Responsibilities * Determine plan of action for incoming calls; * Collect, process, and track incoming adverse and serious adverse events; * Write safety narratives; * Report on various safety data; and * Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes. Qualifications * Bachelor's degree in Healthcare related field; Nursing, Pharmacy, Pharmacology, etc * Clinical experience or Clinical Research, case processing and Post marketing Pharmacovigilance experience is preferred; * Proficient English is required * Proficient knowledge of Microsoft® Office; * Broad knowledge of medical terminology; and * Strong organizational and communication skills. Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company-sponsored employee appreciation events * Employee health and wellness initiatives Awards * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What To Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets

We are currently seeking a full-time, office-based Clinical Safety Coordinator to join our Clinical Safety department in India. This position will be focused on the handling and processing of adverse events from all sources, including clinical trials and post marketing surveillance.If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you!Responsibilities * Determine plan of action for incoming calls; * Collect, process, and track incoming adverse and serious adverse events; * Write safety narratives; * Report on various safety data; and * Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes.      Qualifications * Bachelor's degree in Healthcare related field; Nursing, Pharmacy, Pharmacology, etc * Clinical experience or Clinical Research, case processing and Post marketing Pharmacovigilance experience is preferred; * Proficient English is required * Proficient knowledge of Microsoft® Office; * Broad knowledge of medical terminology; and * Strong organizational and communication skills.      Medpace OverviewMedpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.Why Medpace?People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.Medpace Perks * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company-sponsored employee appreciation events * Employee health and wellness initiatives      Awards * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility      What To Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.EO/AA Employer M/F/Disability/Vets

Drug Safety Specialist - Medpace

We are currently seeking a full-time, office-based Clinical Safety Coordinator to join our Clinical Safety department in India. This position will be focused on the handling and processing of adverse events from all sources, including clinical trials and post marketing surveillance.&lt;br&gt;&lt;br&gt;If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you!&lt;br&gt;&lt;br&gt;&lt;strong&gt;Responsibilities&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Determine plan of action for incoming calls;&lt;/li&gt;&lt;li&gt;Collect, process, and track incoming adverse and serious adverse events;&lt;/li&gt;&lt;li&gt;Write safety narratives;&lt;/li&gt;&lt;li&gt;Report on various safety data; and&lt;/li&gt;&lt;li&gt;Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Qualifications&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Bachelor's degree in Healthcare related field; Nursing, Pharmacy, Pharmacology, etc &lt;/li&gt;&lt;li&gt;Clinical experience or Clinical Research, case processing and Post marketing Pharmacovigilance experience is preferred;&lt;/li&gt;&lt;li&gt;Proficient English is required &lt;/li&gt;&lt;li&gt;Proficient knowledge of Microsoft® Office;&lt;/li&gt;&lt;li&gt;Broad knowledge of medical terminology; and&lt;/li&gt;&lt;li&gt;Strong organizational and communication skills.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Medpace Overview&lt;br&gt;&lt;br&gt;&lt;/strong&gt;Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Why Medpace?&lt;br&gt;&lt;br&gt;&lt;/strong&gt;People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.&lt;br&gt;&lt;br&gt;The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Medpace Perks&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Flexible work environment &lt;/li&gt;&lt;li&gt;Competitive compensation and benefits package&lt;/li&gt;&lt;li&gt;Competitive PTO packages&lt;/li&gt;&lt;li&gt;Structured career paths with opportunities for professional growth&lt;/li&gt;&lt;li&gt;Company-sponsored employee appreciation events &lt;/li&gt;&lt;li&gt;Employee health and wellness initiatives&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Awards&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024&lt;/li&gt;&lt;li&gt;Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;What To Expect Next&lt;br&gt;&lt;br&gt;&lt;/strong&gt;A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.&lt;br&gt;&lt;br&gt;EO/AA Employer M/F/Disability/Vets

Drug Safety Specialist

You need 1 year as CRA/CRC, a science degree, bilingual in English/French, knowledge of clinical trial guidelines, strong communication skills, attention to detail, and 60-80% travel ability.

You will conduct site visits, manage correspondence and files, complete reports, oversee sites, and review patient charts and data throughout the research process.

Science

Toronto

Medpace is growing quickly and we are seeking a Clinical Research Associate to join our team in Canada. We are an innovative, scientifically oriented mid-sized CRO that is focused on full-service project work. This is a home-based position in Canada. Through our PACE Training Program, you will join other Professionals Achieving CRA Excellence and receive customized, expedited training, and efficient onboarding to familiarize experienced CRAs with Medpace systems. WE OFFER THE FOLLOWING * Competitive bonus plans including Resourcing Bonus (following training completion and successful assignment to studies) and Yearly Travel Incentives * Voluntary retirement scheme * Home office furniture allowance, mobile phone and hotspot for internet access anywhere * In-house travel agents, reimbursement for airline club and TSA pre-check * Customized PACE training program based on your experience and therapeutic background and interest * User friendly CTMS with electronic submission and approval of monitoring visit reports * Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts * National assignments with average of 2 protocols * In-house administrative support for all levels of CRAs * Opportunities to work with international team of CRAs * Low turnover rates for CRAs * No metric for minimum required days on site per month * Flexible work hours across days within a week * Opportunity for CRA leadership positions - Lead CRA, CRA Manager * Many additional perks unmatched by other CROs! Responsibilities * Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to Medpace/Sponsor SOPs and GCP; * Maintain ongoing site correspondence and site files; * Complete visit reports and maintaining study-related databases; * Oversight and interaction with clinical research sites; and * Review of patient charts and clinical research data. Qualifications * Minimum 1 year working as a Clinical Research Associate or Clinical Research Coordinator; * Bachelor’s degree in science from an accredited university; * Bilingual in English and French is preferred; * Thorough knowledge of the methodology related to the conduct and monitoring of clinical trials per ICH E-6 guidelines and per Part-C, Division 5 of the Health Canada Food and Drug regulations; * Excellent interpersonal, written and verbal communication skills; * Strong attention to detail and organization skills; * Highly motivated, independent, flexible; * Ability to travel between 60-80%; * Ability to prioritize workload to meet timelines across multiple studies; and * Proficient in Microsoft Office. Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks * Hybrid work-from-home options (dependent upon position and level) * Competitive PTO packages * Company-sponsored employee appreciation events * Employee health and wellness initiatives * Flexible work schedule * Competitive compensation and benefits package * Structured career paths with opportunities for professional growth Awards * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What To Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets

Medpace is growing quickly and we are seeking a Clinical Research Associate to join our team in Canada. We are an innovative, scientifically oriented mid-sized CRO that is focused on full-service project work.This is a home-based position in Canada.Through our PACE Training Program, you will join other Professionals Achieving CRA Excellence and receive customized, expedited training, and efficient onboarding to familiarize experienced CRAs with Medpace systems.WE OFFER THE FOLLOWING * Competitive bonus plans including Resourcing Bonus (following training completion and successful assignment to studies) and Yearly Travel Incentives * Voluntary retirement scheme * Home office furniture allowance, mobile phone and hotspot for internet access anywhere * In-house travel agents, reimbursement for airline club and TSA pre-check * Customized PACE training program based on your experience and therapeutic background and interest * User friendly CTMS with electronic submission and approval of monitoring visit reports * Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts * National assignments with average of 2 protocols * In-house administrative support for all levels of CRAs * Opportunities to work with international team of CRAs * Low turnover rates for CRAs * No metric for minimum required days on site per month * Flexible work hours across days within a week * Opportunity for CRA leadership positions - Lead CRA, CRA Manager * Many additional perks unmatched by other CROs!      Responsibilities * Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to Medpace/Sponsor SOPs and GCP; * Maintain ongoing site correspondence and site files; * Complete visit reports and maintaining study-related databases; * Oversight and interaction with clinical research sites; and * Review of patient charts and clinical research data.      Qualifications * Minimum 1 year working as a Clinical Research Associate or Clinical Research Coordinator; * Bachelor’s degree in science from an accredited university; * Bilingual in English and French is preferred; * Thorough knowledge of the methodology related to the conduct and monitoring of clinical trials per ICH E-6 guidelines and per Part-C, Division 5 of the Health Canada Food and Drug regulations; * Excellent interpersonal, written and verbal communication skills; * Strong attention to detail and organization skills; * Highly motivated, independent, flexible; * Ability to travel between 60-80%; * Ability to prioritize workload to meet timelines across multiple studies; and * Proficient in Microsoft Office.      Medpace OverviewMedpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.Why Medpace?People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.Medpace Perks * Hybrid work-from-home options (dependent upon position and level) * Competitive PTO packages * Company-sponsored employee appreciation events * Employee health and wellness initiatives * Flexible work schedule * Competitive compensation and benefits package * Structured career paths with opportunities for professional growth      Awards * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility      What To Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.EO/AA Employer M/F/Disability/Vets

Clinical Research Associate (CRA) - Canada - Medpace

Clinical Research Associate (CRA) - Canada

You should have a Bachelor’s in Computer Science or IT, 5+ years in IT support, and experience with Exchange Server Tools and Office 365 is beneficial.

You will manage user accounts, provide technical support for IT equipment and software, resolve issues, respond to requests, and collaborate with the IT team for timely solutions.

Customer Relations

IT & Cybersecurity

Munich

Join our growing team in Munich and take your IT support career to the next level! As an IT Support Specialist, you'll have the opportunity to work with cutting-edge technologies, collaborate with international colleagues and develop your skills in a dynamic and global environment, supporting over 400 end users across 6 countries. This is a fully office-based position. Responsibilities * Administrate user accounts for network, e-mail, and other applications; * Provide support to end users on Medpace IT equipment and software applications including computer hardware, peripherals, copiers, fax machines, mobile phones, scanners, building security systems, environment monitoring systems, computer operating systems, office applications; * Identify, research and resolve technical problems of IT equipment and software applications; * Respond to IT tickets, telephone calls, e-mails, and requests for technical support; and * Document, track, and monitor problems to ensure timely resolutions; and * Communicate and collaborate with a regional/global IT team members. Qualifications * Bachelor’s Degree in Computer Science or Information Technology; * Preferbaly 5+ years' experience in a help desk or IT Support role; and * Experience with Exchange Server Tools, Office 365 and other cloud-based applications a plus. Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company-sponsored employee appreciation events * Employee health and wellness initiatives Awards * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What To Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets

Join our growing team in Munich and take your IT support career to the next level! As an IT Support Specialist, you'll have the opportunity to work with cutting-edge technologies, collaborate with international colleagues and develop your skills in a dynamic and global environment, supporting over 400 end users across 6 countries. This is a fully office-based position.Responsibilities * Administrate user accounts for network, e-mail, and other applications; * Provide support to end users on Medpace IT equipment and software applications including computer hardware, peripherals, copiers, fax machines, mobile phones, scanners, building security systems, environment monitoring systems, computer operating systems, office applications; * Identify, research and resolve technical problems of IT equipment and software applications; * Respond to IT tickets, telephone calls, e-mails, and requests for technical support; and * Document, track, and monitor problems to ensure timely resolutions; and * Communicate and collaborate with a regional/global IT team members.      Qualifications * Bachelor’s Degree in Computer Science or Information Technology; * Preferbaly 5+ years' experience in a help desk or IT Support role; and * Experience with Exchange Server Tools, Office 365 and other cloud-based applications a plus.      Medpace OverviewMedpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.Why Medpace?People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.Medpace Perks * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company-sponsored employee appreciation events * Employee health and wellness initiatives      Awards * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility      What To Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.EO/AA Employer M/F/Disability/Vets

IT Support (Munich, Germany) - Medpace

IT Support (Munich, Germany)

You need a Bachelor's in Life Sciences, strong English skills, MS Office knowledge, experience in health/business, plus excellent organization, attention to detail, and prioritization abilities.

You will support the Project Manager, maintain status reports, interact with teams and vendors, manage documentation and supplies, create timelines, and coordinate meetings with minutes.

Due to continuous business growth and a strong study pipeline, we are currently looking to hire Project Coordinators to join our successful and growing German team and engage in clinical trial management on a day-to-day level. This position will work with our operational teams to accomplish tasks and projects that are instrumental to the company’s success. Responsibilities * Work closely with the Project Clinical Trial Manager for timely delivery of recurrent tasks consistently with a high degree of accuracy; * Compile and maintain project-specific status reports within the Clinical Trial Management System (CTMS); * Interact with the internal project team, Sponsor, study sites, and third-party vendors; * Ownership of the Trial Master File; * Manage initial and ongoing site supply shipments; * Create and maintain project timelines and enrolment projections; and * Coordinate project meetings and produce quality minutes. Qualifications * Bachelors’ Degree in Life Sciences, Master’s Degree preferred; * Excellent oral and written English Language communication skills, German knowledge desirable; * Knowledge of Microsoft Office programs; * Experience in a health sciences or business setting preferred; * Excellent organisational and prioritisation skills; * Strong attention to detail; * We kindly ask you to submit your application in English. Medpace Overview Medpace is a full-service clinical contract research organisation (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company-sponsored employee appreciation events * Employee health and wellness initiatives Awards * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What To Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets

Due to continuous business growth and a strong study pipeline, we are currently looking to hire Project Coordinators to join our successful and growing German team and engage in clinical trial management on a day-to-day level. This position will work with our operational teams to accomplish tasks and projects that are instrumental to the company’s success.Responsibilities * Work closely with the Project Clinical Trial Manager for timely delivery of recurrent tasks consistently with a high degree of accuracy; * Compile and maintain project-specific status reports within the Clinical Trial Management System (CTMS); * Interact with the internal project team, Sponsor, study sites, and third-party vendors; * Ownership of the Trial Master File; * Manage initial and ongoing site supply shipments; * Create and maintain project timelines and enrolment projections; and * Coordinate project meetings and produce quality minutes.      Qualifications * Bachelors’ Degree in Life Sciences, Master’s Degree preferred; * Excellent oral and written English Language communication skills, German knowledge desirable; * Knowledge of Microsoft Office programs; * Experience in a health sciences or business setting preferred; * Excellent organisational and prioritisation skills; * Strong attention to detail; * We kindly ask you to submit your application in English.      Medpace OverviewMedpace is a full-service clinical contract research organisation (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.Why Medpace?People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.Medpace Perks * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company-sponsored employee appreciation events * Employee health and wellness initiatives      Awards * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility      What To Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.EO/AA Employer M/F/Disability/Vets

Clinical Project Coordinator - Medpace

Due to continuous business growth and a strong study pipeline, we are currently looking to hire Project Coordinators to join our successful and growing German team and engage in clinical trial management on a day-to-day level. This position will work with our operational teams to accomplish tasks and projects that are instrumental to the company’s success.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Responsibilities&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Work closely with the Project Clinical Trial Manager for timely delivery of recurrent tasks consistently with a high degree of accuracy;&lt;/li&gt;&lt;li&gt;Compile and maintain project-specific status reports within the Clinical Trial Management System (CTMS);&lt;/li&gt;&lt;li&gt;Interact with the internal project team, Sponsor, study sites, and third-party vendors;&lt;/li&gt;&lt;li&gt;Ownership of the Trial Master File;&lt;/li&gt;&lt;li&gt;Manage initial and ongoing site supply shipments;&lt;/li&gt;&lt;li&gt;Create and maintain project timelines and enrolment projections; and&lt;/li&gt;&lt;li&gt;Coordinate project meetings and produce quality minutes.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Qualifications&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Bachelors’ Degree in Life Sciences, Master’s Degree preferred; &lt;/li&gt;&lt;li&gt;Excellent oral and written English Language communication skills, German knowledge desirable;&lt;/li&gt;&lt;li&gt;Knowledge of Microsoft Office programs;&lt;/li&gt;&lt;li&gt;Experience in a health sciences or business setting preferred;&lt;/li&gt;&lt;li&gt;Excellent organisational and prioritisation skills;&lt;/li&gt;&lt;li&gt;Strong attention to detail;&lt;/li&gt;&lt;li&gt;We kindly ask you to submit your application in English.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Medpace Overview&lt;br&gt;&lt;br&gt;&lt;/strong&gt;Medpace is a full-service clinical contract research organisation (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Why Medpace?&lt;br&gt;&lt;br&gt;&lt;/strong&gt;People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.&lt;br&gt;&lt;br&gt;The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Medpace Perks&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Flexible work environment &lt;/li&gt;&lt;li&gt;Competitive compensation and benefits package&lt;/li&gt;&lt;li&gt;Competitive PTO packages&lt;/li&gt;&lt;li&gt;Structured career paths with opportunities for professional growth&lt;/li&gt;&lt;li&gt;Company-sponsored employee appreciation events &lt;/li&gt;&lt;li&gt;Employee health and wellness initiatives&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Awards&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024&lt;/li&gt;&lt;li&gt;Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;What To Expect Next&lt;br&gt;&lt;br&gt;&lt;/strong&gt;A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.&lt;br&gt;&lt;br&gt;EO/AA Employer M/F/Disability/Vets

Clinical Project Coordinator

You need a Bachelor’s in Computer Science/IT, 5+ years in help desk/IT support, and experience with Exchange Server Tools, Office 365, and cloud applications is a plus.

You will manage user accounts, provide IT support for hardware/software, resolve technical issues, handle support requests, document problems, and collaborate with the global IT team.

Software Engineering

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.   * Administrate user accounts for network, e-mail, and other applications; * Provide support to end users on Medpace IT equipment and software applications including computer hardware, peripherals, copiers, fax machines, mobile phones, scanners, building security systems, environment monitoring systems, computer operating systems, office applications; * Identify, research and resolve technical problems of IT equipment and software applications; * Respond to IT tickets, telephone calls, e-mails, and requests for technical support; and * Document, track, and monitor problems to ensure timely resolutions; and * Communicate and collaborate with a regional/global IT team members.   * Bachelor’s Degree in Computer Science or Information Technology; * Preferbaly 5+ years' experience in a help desk or IT Support role; and * Experience with Exchange Server Tools, Office 365 and other cloud-based applications a plus.

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.  * Administrate user accounts for network, e-mail, and other applications; * Provide support to end users on Medpace IT equipment and software applications including computer hardware, peripherals, copiers, fax machines, mobile phones, scanners, building security systems, environment monitoring systems, computer operating systems, office applications; * Identify, research and resolve technical problems of IT equipment and software applications; * Respond to IT tickets, telephone calls, e-mails, and requests for technical support; and * Document, track, and monitor problems to ensure timely resolutions; and * Communicate and collaborate with a regional/global IT team members.  * Bachelor’s Degree in Computer Science or Information Technology; * Preferbaly 5+ years' experience in a help desk or IT Support role; and * Experience with Exchange Server Tools, Office 365 and other cloud-based applications a plus.

&lt;p&gt;&lt;span&gt;Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.&lt;/span&gt;&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;&lt;span&gt;Administrate user accounts for network, e-mail, and other applications;&lt;/span&gt;&lt;/li&gt;&lt;li&gt;&lt;span&gt;Provide support to end users on Medpace IT equipment and software applications including computer hardware, peripherals, copiers, fax machines, mobile phones, scanners, building security systems, environment monitoring systems, computer operating systems, office applications;&lt;/span&gt;&lt;/li&gt;&lt;li&gt;&lt;span&gt;Identify, research and resolve technical problems of IT equipment and software applications;&lt;/span&gt;&lt;/li&gt;&lt;li&gt;&lt;span&gt;Respond to IT tickets, telephone calls, e-mails, and requests for technical support; and&lt;/span&gt;&lt;/li&gt;&lt;li&gt;&lt;span&gt;Document, track, and monitor problems to ensure timely resolutions; and&lt;/span&gt;&lt;/li&gt;&lt;li&gt;&lt;span&gt;Communicate and collaborate with a regional/global IT team members.&lt;/span&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;&lt;span&gt;Bachelor&amp;rsquo;s Degree in Computer Science or Information Technology;&lt;/span&gt;&lt;/li&gt;&lt;li&gt;&lt;span&gt;Preferbaly 5+ years' experience in a help desk or IT Support role; and&lt;/span&gt;&lt;/li&gt;&lt;li&gt;&lt;span&gt;Experience with Exchange Server Tools, Office 365 and other cloud-based applications a plus.&lt;/span&gt;&lt;/li&gt;&lt;/ul&gt;