Gastroenterologist – Clinical Research Role | Flexible Schedule (San Jose, CA)
San Jose, CAFull-time, Part-time, and Contractor
Behavioral Health Market Context
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Benefits
Health Insurance
Job Description
ub-Investigator). This is an excellent opportunity for physicians passionate about advancing medicine through research while maintaining a flexible schedule.
Specialties of Interest
• Dermatology
• Cardiology
• Endocrinology
• Gastroenterology
• Hematology
• Infectious Disease
• Nephrology
• Neurology
• Oncology
• Obesity Medicine
• Pain Management
• PM&R
• Psychiatry
• Pulmonology
• Rheumatology
• Surgery (General & Subspecialties: Orthopedic, Cardiothoracic, etc.)
• Urology
• GI
Key Responsibilities
• Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) on clinical trials.
• Conduct medical screenings, physical examinations, and specialty-specific evaluations for study participants.
• Provide medical oversight and ensure patient safety throughout all trial phases.
• Monitor, document, and report adverse events (AEs/SAEs) in compliance with study protocols and regulatory standards.
• Collaborate with study coordinators, research staff, sponsors, CROs, and IRBs to ensure protocol compliance and data quality.
• Participate in site initiation visits, monitoring visits, audits, and investigator meetings.
• Contribute to protocol feasibility reviews, recruitment strategies, and study design discussions.
• Maintain compliance with GCP, FDA regulations, and institutional guidelines.
• Stay updated on clinical research practices and therapeutic advancements.
Requirements
• MD or DO degree with an active, unrestricted U.S. medical license (Colorado and/or Illinois preferred).
• Board certification in Dermatology or one of the listed specialties.
• DEA license and BLS/ACLS certification preferred.
• Prior clinical research experience strongly preferred (training available for motivated candidates).
• Proficiency with EHR, EDC, CTMS, and medical documentation systems.
• Strong communication and interpersonal skills; ability to thrive in a multidisciplinary, fast-paced environment.
• Commitment to ethical research and patient-centered care.
Compensation & Benefits
• Flexible scheduling: 0-8 hours/week part-time or full-time options.
• Opportunity to participate in cutting-edge clinical trials across multiple therapeutic areas.
• Professional growth in research leadership and investigator experience.
Specialties of Interest
• Dermatology
• Cardiology
• Endocrinology
• Gastroenterology
• Hematology
• Infectious Disease
• Nephrology
• Neurology
• Oncology
• Obesity Medicine
• Pain Management
• PM&R
• Psychiatry
• Pulmonology
• Rheumatology
• Surgery (General & Subspecialties: Orthopedic, Cardiothoracic, etc.)
• Urology
• GI
Key Responsibilities
• Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) on clinical trials.
• Conduct medical screenings, physical examinations, and specialty-specific evaluations for study participants.
• Provide medical oversight and ensure patient safety throughout all trial phases.
• Monitor, document, and report adverse events (AEs/SAEs) in compliance with study protocols and regulatory standards.
• Collaborate with study coordinators, research staff, sponsors, CROs, and IRBs to ensure protocol compliance and data quality.
• Participate in site initiation visits, monitoring visits, audits, and investigator meetings.
• Contribute to protocol feasibility reviews, recruitment strategies, and study design discussions.
• Maintain compliance with GCP, FDA regulations, and institutional guidelines.
• Stay updated on clinical research practices and therapeutic advancements.
Requirements
• MD or DO degree with an active, unrestricted U.S. medical license (Colorado and/or Illinois preferred).
• Board certification in Dermatology or one of the listed specialties.
• DEA license and BLS/ACLS certification preferred.
• Prior clinical research experience strongly preferred (training available for motivated candidates).
• Proficiency with EHR, EDC, CTMS, and medical documentation systems.
• Strong communication and interpersonal skills; ability to thrive in a multidisciplinary, fast-paced environment.
• Commitment to ethical research and patient-centered care.
Compensation & Benefits
• Flexible scheduling: 0-8 hours/week part-time or full-time options.
• Opportunity to participate in cutting-edge clinical trials across multiple therapeutic areas.
• Professional growth in research leadership and investigator experience.
Qualifications
- •This is an excellent opportunity for physicians passionate about advancing medicine through research while maintaining a flexible schedule
- •Dermatology
- •Cardiology
- •Endocrinology
- •Gastroenterology
- •Hematology
- •Infectious Disease
- •Neurology
- •Oncology
- •PM&R
- •Psychiatry
- •Surgery (General & Subspecialties: Orthopedic, Cardiothoracic, etc.)
- •Urology
- •GI
- •Board certification in Dermatology or one of the listed specialties
- •Proficiency with EHR, EDC, CTMS, and medical documentation systems
- •Strong communication and interpersonal skills; ability to thrive in a multidisciplinary, fast-paced environment
- •Commitment to ethical research and patient-centered care
Benefits
- •Schedule: Flexible | Part-Time (0-8 hours/week) or Full-Time options
- •Compensation: Based on specialty, experience, and contract type
- •Obesity Medicine
- •Pain Management
- •Compensation & Benefits
- •Flexible scheduling: 0-8 hours/week part-time or full-time options
- •Opportunity to participate in cutting-edge clinical trials across multiple therapeutic areas
- •Professional growth in research leadership and investigator experience
Responsibilities
- •Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) on clinical trials
- •Conduct medical screenings, physical examinations, and specialty-specific evaluations for study participants
- •Provide medical oversight and ensure patient safety throughout all trial phases
- •Monitor, document, and report adverse events (AEs/SAEs) in compliance with study protocols and regulatory standards
- •Collaborate with study coordinators, research staff, sponsors, CROs, and IRBs to ensure protocol compliance and data quality
- •Participate in site initiation visits, monitoring visits, audits, and investigator meetings
- •Contribute to protocol feasibility reviews, recruitment strategies, and study design discussions
- •Maintain compliance with GCP, FDA regulations, and institutional guidelines
- •Stay updated on clinical research practices and therapeutic advancements
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