Clinical Research Coordinator

Duties:

• Coordination of study protocols under the direction of the Principal Investigator
• Patient-related procedures such as: scheduling and completing participant visits using source documents; vitals, height, weight and ECG collection, phlebotomy/specimen collection; serving as the first point of contact for participant concerns; working with investigational products
• Data entry and maintaining study files
• Communicating with sponsors and meeting sponsor demands
• Traveling for new study start-up up to 4x/year
• The type of employee we are looking for:
• Organized and able to handle fast-paced, occasionally stressful situations
• Calm under pressure and capable of solving sudden problems that may not have clear answers or readily available resources
• Personable
• Trusted to work independently
• An effective communicator who can cooperate as a member of a team
• Ability to prioritize and multitask
• Ability to work within a hierarchy

Required:

• BS/BA, RN, or higher
• Ability to navigate technology and programs independently and adeptly
• COVID-19 Vaccination
• Must be able to commute to both West Chester, PA and Media, PA

Preferred, but not necessary:

• Experience in clinical research
• Background in behavioral techniques, such as a case management worker or therapeutic staff support