Sub-Investigator
Location: Wilson, NC (Onsite)
Type: Direct Hire, Full-time
Responsibilities:
- Reviews, comprehends, and adheres to assigned study protocol.
- Assists trial Investigators in screening and review of potential study participants' eligibility.
- Conducts subject visits.
- Maintains case report forms, patient charts and documentation.
- Ensures that all clinical activities are carried out in accordance with established research protocol and standards in compliance with all applicable laws, regulations, policies, and procedural requirements.
- Collects and enters data as necessary.
- Reviews lab results, imaging reports, and other study-specific reports.
- Completes required protocol training
Requirements:
- Master’s Degree required
- Licensed Nurse Practitioner/Physician Assistant
- At least 2 years of clinical research/ sub-investigator experience is strongly preferred.
- Trained in phlebotomy
- Family med and/or GI experience strongly preferred.
- Sound knowledge of FDA regulations, ICH-Good Clinical Practices (GCP) and ISOs
- Solid teamwork, organizational, interpersonal, attention to detail, and problem-solving skills
- Strong written and verbal communication skills
- Ability to multi-task, work under time constraints, work independently and cooperatively with interdisciplinary teams
- Strong computer skills in appropriate software and related company clinical systems is required
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