Sr. Clinical Trial Manager

3 weeks ago


Boston, United States Proclinical Staffing Full time

Proclinical is seeking a dedicated Senior Clinical Trial Manager (CTM) to join our global Clinical Operations Department. The successful candidate will play a crucial role in managing and executing clinical trials, ensuring compliance with regulations, maintaining timelines, and overseeing data collection and review. The Senior CTM will also be responsible for managing the Clinical Operations study team, Clinical Research Organizations (CROs), and third-party vendors.

Responsibilities:
- Lead day-to-day Clinical Operations activities for a clinical trial, including start-up, maintenance, and closure.
- Manage compliance and quality of a clinical trial, including maintaining accurate documentation of trial progress.
- Define and execute quality control steps, including study quality and performance metrics and reporting.
- Coordinate data review activities required of Clinical Operations team members.
- Contribute to the development of study protocols and understand study protocol objectives.
- Lead development of clinical trial-related documents, including approving and maintaining study plans.
- Conduct study feasibility and ensure proper site selection and setup.
- Manage and drive processes for outsourcing to CROs and other third-party vendors.

Key Skills and Requirements:
- Bachelor's degree in life sciences required; master's degree preferred.
- Relevant clinical operations experience with a focus on trial management.
- Excellent understanding and application of ICH/GCP guidelines.
- Strong interpersonal and communication skills.
- Ability to travel up to 25%.
- Proactive, organized, with attention to detail and excellent problem-solving skills.

If you are having difficulty in applying or if you have any questions, please contact Bo Forsen at b.forsen@proclinical.com

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.



  • Boston, United States Clinical Dynamix Full time

    Responsible for oversight, coordination, and execution of clinical trials in support of clinical operations programs in Phases I‐IV of development.RESPONSIBILITIESClinical Operations team member: works closely with the Sr. CTM and/or Director of Clinical Operations and is responsible for oversight, planning, and execution of assigned clinical studies,...


  • Boston, United States Clinical Dynamix Full time

    Responsible for oversight, coordination, and execution of clinical trials in support of clinical operations programs in Phases I‐IV of development.RESPONSIBILITIESClinical Operations team member: works closely with the Sr. CTM and/or Director of Clinical Operations and is responsible for oversight, planning, and execution of assigned clinical studies,...


  • Boston, United States Argenx SE Full time

    PURPOSE OF THE FUNCTION The Senior Clinical Trial Manager (CTM) is responsible for all operational aspects of the assigned clinical studies from monitoring initiation till closure of the studies. The successful candidate will have clinical trial operational experience in phase I, II and III drug development phases and is an operational expert in the...


  • Boston, United States Argenx SE Full time

    PURPOSE OF THE FUNCTION The Senior Clinical Trial Manager (CTM) is responsible for all operational aspects of the assigned clinical studies from monitoring initiation till closure of the studies. The successful candidate will have clinical trial operational experience in phase I, II and III drug development phases and is an operational expert in the...


  • Boston, United States Argenx Full time

    PURPOSE OF THE FUNCTIONThe Senior Clinical Trial Manager (CTM) is responsible for all operational aspects of the assigned clinical studies from monitoring initiation till closure of the studies. The successful candidate will have clinical trial operational experience in phase I, II and III drug development phases and is an operational expert in the clinical...


  • Boston, United States Argenx Full time

    PURPOSE OF THE FUNCTIONThe Senior Clinical Trial Manager (CTM) is responsible for all operational aspects of the assigned clinical studies from monitoring initiation till closure of the studies. The successful candidate will have clinical trial operational experience in phase I, II and III drug development phases and is an operational expert in the clinical...


  • Boston, United States Meet Full time

    Are you an experienced Clinical Operations professional looking to advance your career in a dynamic and innovative environment? Do you thrive in a fast-paced setting and excel at managing clinical trials from start to finish? If so, we have an exciting opportunity for you to join a prominent biopharmaceutical company dedicated to advancing novel therapies...


  • Boston, United States Meet Full time

    Are you an experienced Clinical Operations professional looking to advance your career in a dynamic and innovative environment? Do you thrive in a fast-paced setting and excel at managing clinical trials from start to finish? If so, we have an exciting opportunity for you to join a prominent biopharmaceutical company dedicated to advancing novel therapies...


  • Boston, United States Proclinical Staffing Full time

    Proclinical is seeking a dedicated Senior Clinical Trial Manager (CTM) to join our global Clinical Operations Department. The successful candidate will play a crucial role in managing and executing clinical trials, ensuring compliance with regulations, maintaining timelines, and overseeing data collection and review. The Senior CTM will also be responsible...


  • Boston, United States ProClinical Full time

    Proclinical is seeking a dedicated Senior Clinical Trial Manager (CTM) to join our global Clinical Operations Department. The successful candidate will play a crucial role in managing and executing clinical trials, ensuring compliance with regulations, maintaining timelines, and overseeing data collection and review. The Senior CTM will also be responsible...


  • Boston, United States Proclinical Staffing Full time

    Proclinical is seeking a dedicated Senior Clinical Trial Manager (CTM) to join our global Clinical Operations Department. The successful candidate will play a crucial role in managing and executing clinical trials, ensuring compliance with regulations, maintaining timelines, and overseeing data collection and review. The Senior CTM will also be responsible...


  • Boston, United States ProClinical Full time

    Proclinical is seeking a dedicated Senior Clinical Trial Manager (CTM) to join our global Clinical Operations Department. The successful candidate will play a crucial role in managing and executing clinical trials, ensuring compliance with regulations, maintaining timelines, and overseeing data collection and review. The Senior CTM will also be responsible...


  • Boston, United States Proclinical Staffing Full time

    Proclinical is seeking a dedicated Senior Clinical Trial Manager (CTM) to join our global Clinical Operations Department. The successful candidate will play a crucial role in managing and executing clinical trials, ensuring compliance with regulations, maintaining timelines, and overseeing data collection and review. The Senior CTM will also be responsible...


  • Boston, United States CRISPR Therapeutics Full time

    Company Overview Since its inception over a decade ago, CRISPR Therapeutics has transformed from a research-stage company advancing programs in the field of gene editing, to a company with a diverse portfolio of product candidates across a broad range of disease areas including hemoglobinopathies, oncology, regenerative medicine, cardiovascular and...


  • Boston, United States Meet Full time

    Are you an experienced Clinical Operations professional looking to advance your career in a dynamic and innovative environment? Do you thrive in a fast-paced setting and excel at managing clinical trials from start to finish? If so, we have an exciting opportunity for you to join a prominent biopharmaceutical company dedicated to advancing novel therapies...


  • Boston, United States Planet Pharma Full time

    MUST HAVEStudy Start upSponsor / Biotech (HIGHLY Preferred)TMF spot check Reviewed monitoring reportsTracking documents for review from CROReview of Pharmacy ManualAble to perform preliminary document reviewHighly Organized and "on the ball"Role summaryThe CTA/ iCRA, reporting to the Director, Clinical Operations, will be responsible for supporting the...


  • Boston, United States Planet Pharma Full time

    MUST HAVEStudy Start upSponsor / Biotech (HIGHLY Preferred)TMF spot check Reviewed monitoring reportsTracking documents for review from CROReview of Pharmacy ManualAble to perform preliminary document reviewHighly Organized and "on the ball"Role summaryThe CTA/ iCRA, reporting to the Director, Clinical Operations, will be responsible for supporting the...


  • Boston, United States Planet Pharma Full time

    MUST HAVEStudy Start upSponsor / Biotech (HIGHLY Preferred)TMF spot check Reviewed monitoring reportsTracking documents for review from CROReview of Pharmacy ManualAble to perform preliminary document reviewHighly Organized and "on the ball"Role summaryThe CTA/ iCRA, reporting to the Director, Clinical Operations, will be responsible for supporting the...


  • Boston, United States Beacon Hill Full time

    Position Overview: Reporting to the Director of Clinical Operations, this individual will have primary responsibility for trial management for a first-in-human trial in both healthy volunteers and patients. This person will manage cross-functional relationships with internal and external stakeholders and be the primary driver of all clinical study related...


  • Boston, United States Beacon Hill Full time

    Position Overview: Reporting to the Director of Clinical Operations, this individual will have primary responsibility for trial management for a first-in-human trial in both healthy volunteers and patients. This person will manage cross-functional relationships with internal and external stakeholders and be the primary driver of all clinical study related...