Entry-Level Clinical Research Coordinator – Trials

Cooper Norcross Health; Camden (NJ); On-site; USD 40,000 - 52,000; Full time

Job summary

Cooper Norcross Health in Camden, NJ seeks a research support role to assist the Principal Investigator and the research team with preparing IRB protocols, consent forms, and developing study budgets. You will complete and maintain study documents, assist with participant identification and recruitment, and collaborate with all study personnel.

0-2 years of research experience is preferred; a Medical Assistant, LPN or Phlebotomist background (or high school/GED) is acceptable.

Qualifications

• Assists with preparation of IRB protocols, consent forms, and study budgets.
• Completes and maintains all study documents as required.
• Assists with identification and recruitment of study participants.
• Works as a team with all involved in the studies.

Responsibilities

• Assist the Principal Investigator and research team with IRB protocol preparation.
• Prepare consent forms and support development of budgets for studies.
• Identify and recruit study participants and maintain study documentation.

Skills

Research experience

Education

High School Diploma or GED

Medical Assistant training

LPN training

Phlebotomy training

Job description

Cooper Norcross Health in Camden, NJ seeks a research support role to assist the Principal Investigator and the research team with preparing IRB protocols, consent forms, and developing study budgets. You will complete and maintain study documents, assist with participant identification and recruitment, and collaborate with all study personnel.

0-2 years of research experience is preferred; a Medical Assistant, LPN or Phlebotomist background (or high school/GED) is acceptable.