CLINICAL RESEARCH COORD I-PRN
Cooper Norcross Health
Camden, NJ0–2 yrs27m agovia LinkedIn
About the Role
Assists the Principal Investigator and other members of the research team with preparation of IRB protocols, consent forms, and development of study budget.
Completes and maintains all study documents as required.
Assists with the identification and recruitment of study participants.
Works as a team player with all involved in the studies.
Qualifications
- Medical Assistant, LPN, or Phlebotomist experience preferred.
- High School Diploma or GED