Part-Time Clinical Research Coordinator
Actalent•New Brunswick, NJ
29d•$25 - $30•Onsite
About The Position
We are seeking a skilled Clinical Research Coordinator with strong experience in clinical research to support a research site involved in an oncology trial. The candidate is expected to be onsite 2-3 days a week.
Requirements
- Experience as a Clinical Research Coordinator.
- Minimum of 2 years of experience in EDC data entry.
- Training in HIPAA & GCP.
- Experience in oncology.
Responsibilities
- Collect and enter data into the Electronic Data Capture (EDC) system.
- Resolve queries related to clinical trial data.
Benefits
- Medical, dental & vision
- Critical Illness, Accident, and Hospital
- 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
- Life Insurance (Voluntary Life & AD&D for the employee and dependents)
- Short and long-term disability
- Health Spending Account (HSA)
- Transportation benefits
- Employee Assistance Program
- Time Off/Leave (PTO, Vacation or Sick Leave)
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What This Job Offers
Job Type
Part-time
Career Level
Entry Level
Industry
Administrative and Support Services
Education Level
No Education Listed
Number of Employees
1,001-5,000 employees
