Part-Time 6 8 Hours/Week Greensboro NC
Position Overview
This is a permanent part-time position requiring approximately 6 8 clinical hours per week (flexible; one weekday morning and one weekday afternoon). The Investigator will provide medical oversight and leadership for ongoing and upcoming clinical trials in Phases II IV. The role involves evaluating participant safety conducting study-related exams and assessments and collaborating closely with our research staff and sponsor partners to ensure the highest standards of clinical and regulatory compliance.
Key Responsibilities
- Serve as Principal Investigator (PI) or Sub-Investigator for assigned clinical trials.
- Provide medical and scientific oversight throughout all stages of the study.
- Evaluate and determine study participant eligibility per protocol criteria.
- Conduct physical examinations and clinical assessments as required.
- Review diagnostic results and provide clinical interpretation and direction to the study team.
- Ensure protocol adherence and regulatory compliance with FDA ICH and GCP standards.
- Collaborate with internal teams in Clinical Operations Regulatory Affairs and Patient Engagement.
- Communicate study-related information clearly to participants and clinical staff.
- Complete all required sponsor and industry training in a timely manner.
Qualifications
- MD or DO currently licensed to practice medicine in the State of North Carolina with no history of license suspension or debarment.
- 2 years of experience as a clinical investigator on pharma-sponsored clinical trials (highly preferred).
- Board certification preferred.
- Excellent interpersonal and communication skills; ability to build rapport with study participants sponsors and team members.
- Strong attention to detail organizational ability and commitment to quality and compliance.
Why Join Us
- Flexible schedule (one weekday morning and one weekday afternoon 6 8 hours/week).
- Opportunity to contribute to innovative research improving patient outcomes.
- Supportive experienced clinical research team.
- Collaborative community-focused environment with a strong reputation for excellence
Part-Time 6 8 Hours/Week Greensboro NC Position Overview This is a permanent part-time position requiring approximately 6 8 clinical hours per week (flexible; one weekday morning and one weekday afternoon). The Investigator will provide medical oversight and leadership for ongoing and upco...
Part-Time 6 8 Hours/Week Greensboro NC
Position Overview
This is a permanent part-time position requiring approximately 6 8 clinical hours per week (flexible; one weekday morning and one weekday afternoon). The Investigator will provide medical oversight and leadership for ongoing and upcoming clinical trials in Phases II IV. The role involves evaluating participant safety conducting study-related exams and assessments and collaborating closely with our research staff and sponsor partners to ensure the highest standards of clinical and regulatory compliance.
Key Responsibilities
- Serve as Principal Investigator (PI) or Sub-Investigator for assigned clinical trials.
- Provide medical and scientific oversight throughout all stages of the study.
- Evaluate and determine study participant eligibility per protocol criteria.
- Conduct physical examinations and clinical assessments as required.
- Review diagnostic results and provide clinical interpretation and direction to the study team.
- Ensure protocol adherence and regulatory compliance with FDA ICH and GCP standards.
- Collaborate with internal teams in Clinical Operations Regulatory Affairs and Patient Engagement.
- Communicate study-related information clearly to participants and clinical staff.
- Complete all required sponsor and industry training in a timely manner.
Qualifications
- MD or DO currently licensed to practice medicine in the State of North Carolina with no history of license suspension or debarment.
- 2 years of experience as a clinical investigator on pharma-sponsored clinical trials (highly preferred).
- Board certification preferred.
- Excellent interpersonal and communication skills; ability to build rapport with study participants sponsors and team members.
- Strong attention to detail organizational ability and commitment to quality and compliance.
Why Join Us
- Flexible schedule (one weekday morning and one weekday afternoon 6 8 hours/week).
- Opportunity to contribute to innovative research improving patient outcomes.
- Supportive experienced clinical research team.
- Collaborative community-focused environment with a strong reputation for excellence
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