Full-Time Research Coordinator

 certification and compliance, subject recruitment, conducting study specific tasks and assessments and adequate enrollment for multiple clinical trials.

Must show strong administrative and time management skills for clinical research.

Previous research experience is desired but not necessary.

Required Qualifications

· Ability to obtain required certifications (GCP, IATA, etc.)

· Must posses the inter personal skills needed to maintain patient retention during all studies.

· Time management skills to coordinate multiple clinical trials simultaneously and conduct multiple patient visits and screenings daily.

Job Duties
• Performing complex subject visits
• Electronic data collection (EDC) programs and ability to complete data entry in a timely manner
• Navigating Institutional Review Board (IRB) submissions, continuing reviews and reports.
• Working with multiple Clinical Research Associates (CRA) to conduct onsite and virtual monitoring visits.
• Project and clinical trial experience including regulatory and compliance responsibilities.
• Source document generation
• Maintaining FDA documentation and regulatory documents

Preferred Qualifications

· Phlebotomy license preferred.

Full Time, Non-Exempt.
• Benefits: Medical, Vision,401K,Paid Holidays, Staff Discounts

Job Type: Full-time

Pay: $25.00 - $35.00 per hour

Benefits:
• 401(k)
• 401(k) matching
• Employee discount
• Flexible spending account
• Health insurance
• Vision insurance

Application Question(s):
• How many years of experience do you have with clinical research/trials?
• Have you used electronic data collection programs?
• Do you have a phlebotomy license?

Education:
• Bachelor's (Preferred)

Work Location: In person