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Clinical Research Project Coordinators

Clinical Research Project Coordinators organize and manage medical studies that test new drugs, devices, or treatments on volunteer patients. They help design the study plan, create data collection forms, set up research sites, schedule patient visits, and train nurses and other staff to follow strict safety and documentation rules. They also track every dose, side effect, and lab result in databases, watch for problems in the protocol, and work with doctors, sponsors, and regulators to keep the study on budget, on schedule, and in full compliance with medical and legal standards.

Clinical Research Project Coordinators

Did you know?

Most positions require a bachelor's degree in life sciences and professional certification from organizations like ACRP or SoCRA to demonstrate competency in clinical research protocols.

At a glance

Typical average pay

$136,400 Avg/yr

Growth

Fast growing

Top skill

Active Listening

Things to consider

Regulatory Compliance Expertise

Success requires thorough knowledge of FDA regulations, Good Clinical Practice guidelines, and HIPAA compliance to ensure trials meet strict American regulatory standards.

Career Growth and Salary Potential

The role offers strong advancement opportunities with median salaries ranging from $45,000-$75,000, with potential progression to senior coordinator or clinical research management positions.

Key responsibilities

  • Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, or potential subject risks.

  • Collaborate with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions.

  • Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts, such as protocol revisions.

  • Maintain contact with sponsors to schedule and coordinate site visits or to answer questions about issues such as incomplete data.

  • Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.

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