Serve as PI or Sub-I across clinical trials in diverse therapeutic areas.
Conduct medical screenings, specialty assessments, and physical examinations.
Ensure participant safety and protocol adherence in compliance with ICH-GCP, FDA, and regulatory standards.
Collaborate with coordinators, nurses, and research staff for accurate documentation and trial execution.
Document patient interactions, monitor adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems.
Engage with sponsors, CROs, monitors, and IRBs to support trial success.
Participate in site initiation visits, monitoring visits, and audits.
Provide medical expertise during feasibility reviews, recruitment strategies, and study design discussions.
Stay updated on clinical research regulations and advances in investigational therapies.
M.D. or D.O. with an active, unrestricted California medical license.
Board-certified in Nephrology
Valid DEA license and current BLS/ACLS certification.
Prior clinical research experience preferred (training available).
Proficiency with EHR systems and clinical trial platforms (EDC, CTMS).
Strong communication and interpersonal skills with a collaborative mindset.
Commitment to ethical, patient-centered research.
Competitive hourly rate: $100 - $250 based on specialty and experience.
Highly flexible, part-time schedule (ideal for supplemental income or work-life balance).
Gain or expand experience in clinical research.
Contribute to the advancement of medical innovation and patient care.
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ProTouch Staffing
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Clinical Research Physician - Long Beach - ProTouch Staffing
Description
Job Description
Clinical Research Physician (Nephrologist) - Long Beach, CA
Schedule: Flexible Part-Time (8 hours per week)
About the Role
We are seeking board-certified Nephrologist to join our Long Beach, CA clinical research site.
This part-time position offers physicians the opportunity to contribute to groundbreaking medical research while maintaining a flexible schedule. You will serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I), overseeing clinical trial activities and ensuring the highest standards of patient safety and protocol compliance across Phase I-IV studies.
Key Responsibilities
Qualifications
Compensation & Benefits
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