Clinical Research Coordinator Job Description

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

Last update : July 14, 2023

Clinical Research Coordinator Job Description

Clinical research coordinators organize, implement, and manage clinical research studies.

Clinical research coordinators manage research projects that involve human subjects.

They typically study diseases or medical conditions that are caused by disease.

Clinical research coordinators may work for pharmaceutical companies, biotechnology or pharmaceutical companies, hospitals, government agencies, or research institutions.

Clinical research coordinators oversee many aspects of clinical research studies, including patient recruitment, data management, and monitoring of patients.

Job Brief:

We’re looking for a Clinical Research Coordinator to join our team and help us conduct important research that could improve the lives of many people. As a Clinical Research Coordinator, you will be responsible for overseeing all aspects of our clinical research studies, from start to finish. This will include working with our team of doctors, nurses, and other medical staff to ensure that our studies are conducted safely and efficiently. If you have a passion for helping others and a strong interest in medical research, then we want you on our team!

Clinical Research Coordinator Duties:

  • Assist in clinical trial recruitment by proactively seeking out potential participants
  • Communicate with clinical professionals, patients, and family members
  • Interview potential participants to assess eligibility
  • Read and research clinical study materials and literature
  • Perform basic administrative tasks related to clinical trials
  • Edit clinical documents and forms
  • Conduct basic administrative functions

Clinical Research Coordinator Responsibilities:

  • Process patient enrollments and data entry, maintain SOP documentation, and report adverse events
  • Conduct pre- and post-study visits with patients to monitor safety and efficacy
  • Provide administrative support for study sponsors or investigators
  • Generate and maintain SOPs and training materials
  • Update and manage documentation in electronic databases
  • Conduct patient surveys, perform data compilation and analysis, and submit reports to sponsors
  • Assist in clinical trial recruitment

Requirements And Skills:

  • Bachelor’s degree in medical or related field
  • 1+ years’ clinical research experience
  • Strong team player with excellent interpersonal skills
  • Ability to maintain accurate and organized records
  • Effective communicator and presenter
  • Highly proficient with electronic medical records

At [Company Name], we believe that diversity and inclusion are key to success. We are committed to building a team that is reflective of the many different backgrounds, perspectives, and experiences that make up our community. We encourage applications from people of all races, religions, national origins, genders, and ages, as well as veterans and individuals with disabilities.

Share this article :