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.
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
Reading Comprehension
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
Participate in the development of study protocols including guidelines for administration or data collection procedures.
Solicit industry-sponsored trials through contacts and professional organizations.
Direct the requisition, collection, labeling, storage, or shipment of specimens.
Develop advertising and other informational materials to be used in subject recruitment.
Arrange for research study sites and determine staff or equipment availability.