MR is looking for a Clinical Research Coordinator to manage clinical research protocols. This individual will work directly with the investigators, and other research staff to ensure protocol visits are being conducted according to ICH GCP guidelines.
Duties
- Comprehend study design of each protocol that is assigned
- Perform procedures in compliance with the study protocol
- Recruit and screen study subjects according to specific protocol requirements
- Collect and record study data in source documents via electronic system (CRIO)
- Manage study related activities
- Adherence to protocol requirements
- Review laboratory data
- Assess and document compliance
- Manage investigational product
- Assess, record, and report Adverse Events as outlined in the protocol
- Manage/train ancillary staff
. Requirements:Qualifications
Education:
- Experience and training in conducting clinical trials with knowledge of ICH GCP
OR
- Two years of college in a health-related program or LPN
- Phlebotomy Skills
Benefits:
Health insurance
- Paid time off
- Dental insurance
- 401(k)
- Vision insurance
- Bonus
Key Words: Clinical Research, Research Coordinator, Research Assistant, Medical Assistant, Coordinator, Certified Medical Assistant, Phlebotomist, Medical, Health Care, Medical Office, Phlebotomy, Assistant, Medical Research, Laboratory Medical
Job Types: Full-time, Contract
Pay: $17.00 - $25.00 per hour
Benefits:
- 401(k)
- Dental insurance
- Health insurance
- Life insurance
- Paid time off
- Vision insurance
Schedule:
Experience:
- Clinical Research Associates & Coordinators: 1 year (Required)
- Medical Assistant/Coordinator: 1 year (Required)
Work Location: In person