Clinical Research Coordinator

Must Haves

Must have 2+ years of CRC experience working as a clinical research Coordinator, ideally have experience working as the sole coordinator

40 hours per week, Monday-Friday 9am-5pm, fully onsite

Medical, Dental, Vision, time off, paid holidays, bonus, 401k, growth opportunities (into Site Director role), etc.

Main responsibilities include patient recruitment, enrollment, consenting, conducting patient visits, and entering data into the EDC. The site currently has 3-4 trials (8 active patients, with potential to increase enrollment following a clean monitoring report) and a cap of 5 total trials. (

Note:

Director will handle startup, budgets, and most regulatory duties remotely).

2 to 3 years of clinical research experience. Must have industry/pharmaceutical-sponsored experience (hospital-only research is not sufficient). Must be GCP (Good Clinical Practice) and IATA trained.

Phlebotomy experience (highly preferred as the current backup cannot draw blood), Medical Assistant (MA) background (familiarity with medical terminology, vitals, EKGs), and Dermatology experience.

An independent, proactive coordinator capable of seeing the bigger clinical picture, taking initiative, spotting medical trends (e.g., bad EKGs), and eventually stepping into a Site Manager role.

High level of patience, tact, and professionalism. Must be able to manage professional relationships diplomatically and work with a disorganized Sub-Investigator without letting personal feelings show through.