What does a Clinical Research Coordinator do?
Learn all about Clinical Research Coordinator duties, skills and much more. Get expert advice on how to become a Clinical Research Coordinator.
Published 3 min read
A Clinical Research Coordinator is responsible for the coordination and management of clinical research studies. They work with investigators to develop study protocols, identify and recruit participants, and ensure that studies are conducted according to protocol. They also collect and manage data, monitor participant safety, and report results.
Clinical Research Coordinator job duties include:
- Identifies potential subjects for clinical research studies.
- Informs subjects of study purpose, procedures, risks and benefits.
- Obtains informed consent from subjects.
- Schedules and monitors subject participation in studies.
- Collects data from subjects according to protocol.
- Maintains accurate and complete study records.
- Assists with the development of clinical research protocols.
- Coordinates the activities of the clinical research team.
- Monitors compliance with federal regulations and institutional policies.
- Performs quality control checks on data collected.
Clinical Research Coordinator Job Requirements
A Clinical Research Coordinator (CRC) is responsible for the day-to-day operations of a clinical research study. A CRC works with the Principal Investigator (PI) to develop the protocol, obtain IRB approval, and recruit and screen participants. A CRC also manages the study budget, monitors participant safety, and ensures that data is collected and recorded accurately.
Most CRC positions require a bachelor’s degree in a scientific discipline, such as biology or nursing. Some employers may prefer candidates who have a master’s degree or certification in clinical research. Many CRC positions also require at least 2 years of experience working in a clinical research setting.
Clinical Research Coordinator Skills
- Strong communication skills
- Organizational skills
- Time management skills
- Writing skills
- Research skills
- Data analysis skills
- Critical thinking skills
- Problem-solving skills
- Detail oriented
- Team player
How to become a Clinical Research Coordinator
A Clinical Research Coordinator (CRC) is a professional who manages and oversees clinical trials. As a CRC, you will be responsible for ensuring that trials are conducted according to protocol and that patient safety is always a priority. In order to become a CRC, you will need to have at least a bachelor’s degree in a health-related field. Additionally, experience in research and/or the healthcare industry is highly beneficial. Strong communication and organizational skills are essential in this role, as you will be coordinating between different teams and individuals. If you are interested in becoming a CRC, start by researching clinical trials that are currently recruiting participants. Once you find a trial that you are eligible for, reach out to the study coordinator and express your interest in being involved. From there, you can inquire about any open positions or volunteer opportunities that may be available.