What are the responsibilities and job description for the Principal Investigator position at Proclinical Staffing?
Principal Investigator - Contract - Oceanside, CA
Lead cutting-edge clinical research while delivering exceptional patient care at the forefront of medical innovation.
Proclinical is seeking a Principal Investigator to oversee clinical trials at an assigned site in the US. This position is ideal for a physician passionate about direct patient interaction and committed to advancing therapeutic options through clinical research.
Primary Responsibilities:
The successful candidate will provide medical expertise and leadership to ensure safe, high-quality research while maintaining a patient-centered approach. You will evaluate participants for eligibility, monitor their safety and well-being, and ensure compliance with protocols and regulatory standards.
Skills & Requirements:
- MD or DO with an active, unrestricted California medical license.
- Experience conducting clinical research with knowledge of ICH-FDA-GCP guidelines and regulatory requirements.
- Proven ability to lead and collaborate with a multidisciplinary clinical research team.
- Strong communication skills with patients, caregivers, clinical staff, and sponsor representatives.
- High ethical standards, professional integrity, and a passion for direct patient care.
- Preferred: Established relationships with community physicians or patient populations in the San Diego area.
- Preferred: Familiarity with CTMS platforms and electronic data capture systems.
The Principal Investigator's responsibilities will be:
- Serve as the physician of record for clinical trials, ensuring safe and compliant study conduct.
- Evaluate participants for enrollment eligibility and monitor their safety and response to therapy throughout the trial.
- Provide clinical leadership and oversight to the on-site research team, delegating responsibilities appropriately.
- Maintain thorough knowledge of each protocol, including visit schedules, endpoint criteria, and investigational product requirements.
- Oversee informed consent processes, adverse event documentation, and required safety reporting to sponsors and IRBs.
- Ensure data accuracy and completeness across case report forms and source documents.
- Support site readiness for monitoring visits and audits.
- Collaborate effectively with sponsors, IRBs, and the research team throughout the trial lifecycle.
If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at j.cerchio@proclinical.com.
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy