Our Clinical Research Manager job description includes the responsibilities, duties, skills, education, qualifications, and experience.
About the Clinical Research Manager role
Clinical Research Managers are responsible for planning, coordinating, and directing clinical research projects in the pharmaceutical and biotechnology industries. They monitor the progress of clinical trials and ensure compliance with government regulations. They also recruit and train clinical trial staff, review and analyze research data, and communicate with research sponsors and other stakeholders.
Role Purpose
The purpose of a Clinical Research Manager is to plan, coordinate, and oversee a variety of clinical research projects. They ensure that studies are conducted in accordance with applicable regulatory requirements, ethical standards, and good clinical practice guidelines. Clinical Research Managers also provide guidance and support to research staff, participating sites, and sponsors, and work to ensure that research projects are completed on time and within budget. Additionally, they are responsible for managing data collection, analysis, and reporting, as well as for preparing and submitting study documentation to regulatory agencies.
Clinical Research Manager Summary
The Clinical Research Manager is responsible for the execution and oversight of clinical research studies. This includes the design, implementation and management of clinical research studies from start to finish. The Clinical Research Manager is responsible for identifying and assessing potential study sites, developing protocols, obtaining regulatory and ethical approvals, developing study budgets, recruiting study participants, collecting and analyzing data, and reporting results. Additionally, the Clinical Research Manager will ensure compliance with all applicable research regulations and laws. The ideal candidate should possess strong analytical, problem-solving, and organizational skills.
Clinical Research Manager Duties
- Plan and coordinate clinical studies, managing timelines and resources
- Develop, review and manage clinical trial protocols and related documents
- Ensure clinical studies comply with relevant regulations and standards
- Monitor clinical data to ensure accuracy and quality
- Provide regular updates on clinical study status
- Interact with investigators and other stakeholders
- Prepare and present clinical study results
Clinical Research Manager Skills
- Organizational and project management
- Strong communication and interpersonal skills
- Knowledge of relevant regulations and requirements
- Ability to train and manage staff
- Knowledge of clinical research terminology and processes
Clinical Research Manager Requirements
- Bachelor's degree in a relevant field
- Strong attention to detail
- Project management experience
- Ability to work independently
- Knowledge of clinical research processes
Personal Traits
- Organizational skills
- Strong communication skills
- Ability to manage budgets
- Ability to interpret data
- Attention to detail