Elite Clinical Network
The role involves serving as a Principal Investigator or Sub-Investigator on multiple Phase I–IV clinical trials, conducting comprehensive physical exams and clinical assessments, and providing medical oversight for clinical trial participants. The position requires collaboration with clinical research teams to ensure protocol compliance and data integrity while managing patient care within a clinical research setting.
Key Responsibilities
- • Serve as Principal Investigator or Sub-Investigator on multiple Phase I–IV clinical trials.
- • Perform comprehensive physical exams and clinical assessments for protocol screening and enrollment.
- • Evaluate patient eligibility based on inclusion/exclusion criteria of clinical protocols.
- • Provide medical oversight for clinical trial participants, including safety assessments, adverse event evaluations, and ongoing care.
- • Collaborate closely with Clinical Research Coordinators, Sponsors, and Monitors to ensure protocol compliance and data integrity.
- • Review and sign off on source documents, case report forms (CRFs), and regulatory documentation.
- • Maintain detailed and accurate clinical trial documentation in compliance with ICH-GCP, FDA, and sponsor requirements.
- • Participate in Site Initiation Visits (SIVs), Monitoring Visits, and Audits as needed.
- • Manage chronic and acute conditions among study participants in alignment with standard care and protocol guidelines.
- • Educate and counsel patients on study procedures, informed consent, and potential side effects.
- • Support recruitment efforts and promote patient retention in trials.
Required
- • MD or DO degree from an accredited medical school.
- • Valid, unrestricted medical license in the state of employment.
- • Board Certified or Board Eligible (BC/BE) in Psychiatry.
- • BC/BE in Family Medicine or Geriatric Medicine will also be considered.
- • Current Good Clinical Practice (GCP) certification or willingness to obtain prior to start.
- • Minimum of 1 year of experience in clinical practice; prior clinical research experience preferred but not required.
Preferred
- • Familiarity with FDA, ICH-GCP, and clinical trial protocols.
- • Experience managing or participating in industry-sponsored clinical trials.
- • Strong attention to detail and ability to document accurately.
- • Excellent interpersonal and communication skills for patient interaction and sponsor collaboration.
- • Ability to work collaboratively with a cross-functional team in a fast-paced research environment.
- • Comfortable using electronic medical records (EMRs) and clinical trial management systems (CTMS).
- • DEA license (preferred).
Company Overview
Industry: Healthcare Technology
Company Size: 500-1,000 employees
Founded: 2015
Headquarters: San Francisco, CA
Company Links
Key Contacts
Contact information not available
About the Company
Leading healthcare technology company focused on improving patient outcomes through innovative digital solutions. We're transforming the way healthcare is delivered with cutting-edge technology and data-driven insights. Our platform serves over 10,000 healthcare professionals and has processed millions of patient interactions.
Recent News & Updates
Elite Clinical Network (ECN) is seeking a dedicated and research-oriented Physician – Psychiatrist to join our expanding team of clinical professionals. The ideal candidate will play a critical role in the conduct of clinical trials by serving as a Principal Investigator (PI) or Sub-Investigator, while continuing to provide high-quality medical care to adult patients within a clinical research setting. This is a part time/per diem position with a unique opportunity to contribute to the advancement of medicine through clinical studies.
Key Responsibilities
- Serve as Principal Investigator or Sub-Investigator on multiple Phase I–IV clinical trials.
- Perform comprehensive physical exams and clinical assessments for protocol screening and enrollment.
- Evaluate patient eligibility based on inclusion/exclusion criteria of clinical protocols.
- Provide medical oversight for clinical trial participants, including safety assessments, adverse event evaluations, and ongoing care.
- Collaborate closely with Clinical Research Coordinators, Sponsors, and Monitors to ensure protocol compliance and data integrity.
- Review and sign off on source documents, case report forms (CRFs), and regulatory documentation.
- Maintain detailed and accurate clinical trial documentation in compliance with ICH-GCP, FDA, and sponsor requirements.
- Participate in Site Initiation Visits (SIVs), Monitoring Visits, and Audits as needed.
- Manage chronic and acute conditions among study participants in alignment with standard care and protocol guidelines.
- Educate and counsel patients on study procedures, informed consent, and potential side effects.
- Support recruitment efforts and promote patient retention in trials.
- MD or DO degree from an accredited medical school.
- Valid, unrestricted medical license in the state of employment.
- Board Certified or Board Eligible (BC/BE) in Psychiatry.
- BC/BE in Family Medicine or Geriatric Medicine will also be considered.
- Current Good Clinical Practice (GCP) certification or willingness to obtain prior to start.
- Minimum of 1 year of experience in clinical practice; prior clinical research experience preferred but not required.
- Familiarity with FDA, ICH-GCP, and clinical trial protocols.
- Experience managing or participating in industry-sponsored clinical trials.
- Strong attention to detail and ability to document accurately.
- Excellent interpersonal and communication skills for patient interaction and sponsor collaboration.
- Ability to work collaboratively with a cross-functional team in a fast-paced research environment.
- Comfortable using electronic medical records (EMRs) and clinical trial management systems (CTMS).
- DEA license (preferred).
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