Donor Research Coordinator jobs in Daytona Beach, FL

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

Medical specialties:

• Rheumatology

Schedule:

• Monday to Friday

Work setting:

• In-person

Experience:

• Medical Assistant/Coordinator: 1 year (Required)
• Clinical Research Associates & Coordinators: 1 year (Preferred)

Work Location: In person