Clinical Research Physician (Internal Medicine)
ProTouch Staffing
180–200 an hour
Behavioral Health Market Context
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Job Description
ompliance, and regulatory adherence while collaborating closely with research teams, sponsors, and CROs. The physician will provide clinical oversight for dermatology-focused and multi-therapeutic studies in a professional research environment.
Key Responsibilities:
Serve as PI or Sub-I on assigned clinical trials.
Conduct medical screenings, physical examinations, and participant assessments.
Ensure compliance with study protocols, ICH-GCP guidelines, and regulatory standards.
Monitor patient safety, including documentation and management of AEs/SAEs.
Review and approve study-related documentation in EHR/EDC/CTMS systems.
Collaborate with coordinators, nurses, and research staff to ensure data accuracy and protocol adherence.
Participate in site initiation visits (SIVs), monitoring visits, audits, and investigator meetings.
Support feasibility assessments, recruitment strategies, and study implementation.
Maintain professional relationships with sponsors, CROs, monitors, and IRBs.
Stay current with advancements in clinical research and therapeutic areas.
Qualifications:
MD or DO with an active, unrestricted Colorado medical license.
Board Certification in Internal Medicine.
Active DEA license and current BLS/ACLS certification.
Prior clinical research experience preferred (training available for motivated candidates).
Proficiency with EHR systems and clinical research platforms (EDC/CTMS).
Strong clinical judgment, communication skills, and attention to detail.
For more information, please reach out to Riju : at (469) 378-4213 or by Email: at [email protected].
Key Responsibilities:
Serve as PI or Sub-I on assigned clinical trials.
Conduct medical screenings, physical examinations, and participant assessments.
Ensure compliance with study protocols, ICH-GCP guidelines, and regulatory standards.
Monitor patient safety, including documentation and management of AEs/SAEs.
Review and approve study-related documentation in EHR/EDC/CTMS systems.
Collaborate with coordinators, nurses, and research staff to ensure data accuracy and protocol adherence.
Participate in site initiation visits (SIVs), monitoring visits, audits, and investigator meetings.
Support feasibility assessments, recruitment strategies, and study implementation.
Maintain professional relationships with sponsors, CROs, monitors, and IRBs.
Stay current with advancements in clinical research and therapeutic areas.
Qualifications:
MD or DO with an active, unrestricted Colorado medical license.
Board Certification in Internal Medicine.
Active DEA license and current BLS/ACLS certification.
Prior clinical research experience preferred (training available for motivated candidates).
Proficiency with EHR systems and clinical research platforms (EDC/CTMS).
Strong clinical judgment, communication skills, and attention to detail.
For more information, please reach out to Riju : at (469) 378-4213 or by Email: at [email protected].
Qualifications
- •MD or DO with an active, unrestricted Colorado medical license
- •Board Certification in Internal Medicine
- •Active DEA license and current BLS/ACLS certification
- •Proficiency with EHR systems and clinical research platforms (EDC/CTMS)
- •Strong clinical judgment, communication skills, and attention to detail
Benefits
Responsibilities
- •Clinical Research Physician (Internal Medicine) - 0-8 Hours per Week
- •Schedule: Flexible Part-Time (0-8 hours per week)
- •This role focuses on ensuring patient safety, protocol compliance, and regulatory adherence while collaborating closely with research teams, sponsors, and CROs
- •The physician will provide clinical oversight for dermatology-focused and multi-therapeutic studies in a professional research environment
- •Serve as PI or Sub-I on assigned clinical trials
- •Conduct medical screenings, physical examinations, and participant assessments
- •Ensure compliance with study protocols, ICH-GCP guidelines, and regulatory standards
- •Monitor patient safety, including documentation and management of AEs/SAEs
- •Review and approve study-related documentation in EHR/EDC/CTMS systems
- •Collaborate with coordinators, nurses, and research staff to ensure data accuracy and protocol adherence
- •Participate in site initiation visits (SIVs), monitoring visits, audits, and investigator meetings
- •Support feasibility assessments, recruitment strategies, and study implementation
- •Maintain professional relationships with sponsors, CROs, monitors, and IRBs
- •Stay current with advancements in clinical research and therapeutic areas
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