Clinical Trial Physician (Specialized Fields) at Protouch Staffing Pomona, CA
Behavioral Health Market Context
Apply Nowvia The Art Of Ed Whitmore
Benefits
Health Insurance
Job Description
g clinical trials:
• Endocrinologist/Obesity Medicine
Physicians will oversee study participants, ensure protocol compliance, monitor patient safety, and collaborate with research teams to deliver high-quality trial outcomes.
Key Responsibilities
• Serve as Sub-Investigator or Principal Investigator
• Conduct medical evaluations and assess participant eligibility
• Monitor patient safety, adverse events, and outcomes
• Review and sign study-related documentation
• Collaborate with research coordinators and staff
• Maintain compliance with Good Clinical Practice (GCP)
Qualifications
• MD or DO with an active state medical license
• Board-certified in one of the listed specialties
• Clinical research interest (experience preferred)
• Strong communication and organizational skills
Compensation & Benefits
• Flexible scheduling (0-8 hrs/week)
• Research training and professional growth opportunities
• Impactful contribution to advancing medical science
For more details:
Contact: ???? 469-991-3805 (or) Email me at: [email protected]
Company Description
We are one of the leading healthcare staffing companies in the US. Our ethos is to deliver the best healthcare staffing solutions to both job seekers and employers.
The experts at Protouch are specialized in sourcing highly skilled healthcare professionals. Company Description
We are one of the leading healthcare staffing companies in the US. Our ethos is to deliver the best healthcare staffing solutions to both job seekers and employers.
The experts at Protouch are specialized in sourcing highly skilled healthcare professionals.
• Endocrinologist/Obesity Medicine
Physicians will oversee study participants, ensure protocol compliance, monitor patient safety, and collaborate with research teams to deliver high-quality trial outcomes.
Key Responsibilities
• Serve as Sub-Investigator or Principal Investigator
• Conduct medical evaluations and assess participant eligibility
• Monitor patient safety, adverse events, and outcomes
• Review and sign study-related documentation
• Collaborate with research coordinators and staff
• Maintain compliance with Good Clinical Practice (GCP)
Qualifications
• MD or DO with an active state medical license
• Board-certified in one of the listed specialties
• Clinical research interest (experience preferred)
• Strong communication and organizational skills
Compensation & Benefits
• Flexible scheduling (0-8 hrs/week)
• Research training and professional growth opportunities
• Impactful contribution to advancing medical science
For more details:
Contact: ???? 469-991-3805 (or) Email me at: [email protected]
Company Description
We are one of the leading healthcare staffing companies in the US. Our ethos is to deliver the best healthcare staffing solutions to both job seekers and employers.
The experts at Protouch are specialized in sourcing highly skilled healthcare professionals. Company Description
We are one of the leading healthcare staffing companies in the US. Our ethos is to deliver the best healthcare staffing solutions to both job seekers and employers.
The experts at Protouch are specialized in sourcing highly skilled healthcare professionals.
Qualifications
- •Start Date: Within 0-6 months
- •MD or DO with an active state medical license
- •Board-certified in one of the listed specialties
- •Strong communication and organizational skills
Benefits
- •Compensation & Benefits
- •Flexible scheduling (0-8 hrs/week)
- •Research training and professional growth opportunities
- •Impactful contribution to advancing medical science
Responsibilities
- •Endocrinologist/Obesity Medicine
- •Physicians will oversee study participants, ensure protocol compliance, monitor patient safety, and collaborate with research teams to deliver high-quality trial outcomes
- •Serve as Sub-Investigator or Principal Investigator
- •Conduct medical evaluations and assess participant eligibility
- •Monitor patient safety, adverse events, and outcomes
- •Review and sign study-related documentation
- •Collaborate with research coordinators and staff
- •Maintain compliance with Good Clinical Practice (GCP)
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