What are the responsibilities and job description for the Clinical Research Nephrologist position at Protouch Staffing?
Job Title: Part-Time Clinical Research Nephrologist
Compensation: $100 - $250 per hour
Schedule: Part-Time (0-8 hours)
start date: 0-6 months
About The Role
We are seeking a board-certified to serve as a Clinical Research gastroenterologist
You will oversee protocol compliance, ensure patient safety, and collaborate with sponsors, CROs, and cross-functional teams to drive the success of Phase I-IV clinical trials.
Key Responsibilities
Compensation: $100 - $250 per hour
Schedule: Part-Time (0-8 hours)
start date: 0-6 months
About The Role
We are seeking a board-certified to serve as a Clinical Research gastroenterologist
You will oversee protocol compliance, ensure patient safety, and collaborate with sponsors, CROs, and cross-functional teams to drive the success of Phase I-IV clinical trials.
Key Responsibilities
- Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for dermatology-focused and multi-therapeutic clinical trials.
- Conduct medical screenings, dermatological assessments, and physical examinations for study participants.
- Provide clinical oversight and medical care to study subjects in accordance with protocols, ICH-GCP, and regulatory requirements.
- Collaborate with study coordinators, nurses, and research staff to ensure compliance and accurate documentation.
- Document all patient interactions, adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems.
- Establish and maintain strong working relationships with sponsors, CROs, monitors, and IRBs.
- Participate in site initiation visits (SIVs), monitoring visits, and audits.
- Contribute to protocol feasibility reviews, study design input, and recruitment strategies.
- Attend investigator meetings and provide medical expertise on dermatology-related endpoints and safety monitoring.
- Stay current on clinical research regulations and advances in dermatology and investigational therapies.
- M.D. or D.O. with an active, unrestricted NC medical license.
- Board certification in required.
- Valid DEA license and BLS/ACLS certification.
- Prior experience in clinical research/clinical trials strongly preferred (training available for motivated candidates).
- Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS).
- Strong interpersonal and communication skills with the ability to work in a multidisciplinary, fast-paced environment.
- Commitment to ethical research practices and patient-centered care.
- Competitive hourly rate: $100 - $250 based on experience.
- Flexible part-time schedule.
Salary : $100 - $250