Part-Time Bilingual Clinical Research Coordinator
About The Position
Looking to hire an individual with clinical research experience to act as a consultant CRC to support an ongoing clinical trial. The main job duties for this position will be chart review, phone screening and patient recruitment. This CRC must be experienced in being able to work independently. You will act as one of the main CRC's for this study. Please note, as the position and study progress, additional job duties will likely be added that are not listed in this description. A candidate must be flexible to help the site and study wherever needed. This role requires research experience
Requirements
- Minimum of 2+ years' experience as a Clinical Research Coordinator.
- Electronic medical records (EMR) systems
- Proven track record in patient recruitment for clinical trials.
Responsibilities
- Medical Record Review: Conduct thorough reviews of patient medical records.
- Participant Screening: Perform phone screenings or prescreen participants for eligibility.
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
Mid Level
Industry
Administrative and Support Services
Education Level
No Education Listed
Number of Employees
1,001-5,000 employees
