Clinical Trial Manager Job Description

clinical trial manager job description includes a detailed overview of the key requirements, duties, responsibilities, and skills for this role.

Last update : July 14, 2023

Clinical Trial Manager Job Description

A clinical project manager is a type of manager that organizes and manages clinical trials.

Clinical project managers coordinate all elements of clinical trials, including planning, tracking, budget, and contract management.

Clinical project managers oversee the planning, organization, management, and execution of clinical trials for any new product.

They also set up and maintain clinical trial management systems that are used by study coordinators and monitors.

Clinical project managers often work with prospective trial patients or study coordinators.

Clinical project managers also serve as a liaison between sponsors and contract research organizations (CROs).

CROs help sponsors design and execute

Job Brief:

We’re looking for a Clinical Trial Manager who can help us to organize and manage the clinical work.

Clinical Trial Manager Duties:

  • Manage the recruitment and enrollment of participants in clinical trials
  • Identify, cultivate, and maintain relationships with healthcare providers, physicians, research physicians, patients, and patients’ caregivers
  • Communicate with study sponsors, published sources, and researchers regarding enrollment requirements, clinical trial regulations, and timelines
  • Design, implement, and track processes, protocols, and timelines for ongoing projects
  • Manage reminder/recall lists for participants
  • Maintain databases, spreadsheets, and documents for ongoing projects

Clinical Trial Manager Responsibilities:

  • Operate and coordinate clinical trials involving human subjects, including obtaining and maintaining physiological data, overseeing preparation and storage of study materials, and directing equipment, personnel, and supplies
  • Monitor activities at assigned study sites, identify problems, and resolve issues
  • Prepare reports for funding agencies, sponsors, and regulatory bodies
  • Perform statistical analyses on collected data
  • Develop study protocols and budgets
  • Maintain and manage project schedules
  • Maintain professional relationships with healthcare practitioners, governmental and regulatory agencies, and sponsor representatives
  • Maintain professional documentation

Requirements And Skills:

  • Bachelor’s degree in biology, nursing, or a related field
  • 3+ years’ proven experience in clinical research operations
  • Experience with clinical research-related software
  • Strong knowledge of Good Clinical Practice and federal regulations
  • Proven ability to run clinical trials from first concept through completion

At [Company Name], we believe that a diverse and inclusive team is key to success. We encourage applications from people of all races, religions, national origins, genders, and ages, as well as veterans and individuals with disabilities.

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