Busy clinical research site seeking an experienced Clinical Research Coordinator (CRC) to join our research team. Applicant must have at least 1 year experience as a CRC conducting Pharmaceutical-Sponsored Clinical Trials. Be self-motivated and organized. Able to work independently yet as part of a team in a fast-paced environment.
Responsibilities:
Under the direction and guidance of the PI and Clinical Research Site Manager, the CRC will be responsible for facilitating, coordinating, conducting, and documenting all aspects of the clinical studies from start to successful completion in accordance with the study Protocols, Sponsor requirements and Site SOP’s. (Recruitment and regulatory support are provided.)
Qualifications:
- Bachelor’s degree or equivalent medical experience
- At least 1 year of experience as a Clinical Research Coordinator is required
- Good knowledge of medical terminology and pharmaceutical sciences
- Excellent interpersonal and presentation skills to effectively work with clinicians, patients, administrators, auditors, and sponsor representatives.
- Proficient computer skills, Word, Excel, data and software programs
- Ability to multi-task while focusing on attention to detail
- Exceptional organizational skills to independently manage workflow
- Clinical skills including Phlebotomy, ECG and vital signs collection experience or willingness to learn is a plus.
- Current documentation of GCP, IATA, OHRP, and HIPAA training a plus
Competitive pay based on Clinical Research experience
Job Type: Full-time
Pay: $36,500.00 - $75,000.00 per year
Benefits:
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Schedule:
Application Question(s):
- Live in or able to commute to the Winter Haven, FL area
Education:
Experience:
- Clinical Research Coordinator: 2 years (Preferred)
Location:
- Winter Haven, FL 33880 (Preferred)
Work Location: In person
