About the Role
The role involves conducting health assessments, managing study-related medical procedures, ensuring regulatory compliance, and supporting research protocols under physician oversight.
Responsibilities
- Perform physical exams and medical evaluations for research participants
- Collect and document clinical data according to study protocols
- Ensure adherence to safety and regulatory standards
- Administer study-related treatments or interventions
- Monitor participant health and report adverse events
- Collaborate with research coordinators and physicians
- Maintain accurate and timely medical records
- Review inclusion and exclusion criteria for participant screening
- Support protocol-specific procedures and testing
- Provide education to participants about study requirements
- Assist in the development of clinical procedures
- Participate in site visits and sponsor meetings
- Ensure proper handling of investigational products
- Follow ethical guidelines for human subject research
- Contribute to audit and inspection readiness
Nice to Have
- Prior experience in clinical trials
- Exposure to early-phase or outpatient research
- Background in internal medicine or primary care
- Experience with lab and ECG interpretation
- Training in research ethics and compliance
- Familiarity with adverse event reporting
- Previous work in a research-intensive setting
Compensation
Competitive hourly rate
Work Arrangement
On-site with flexible scheduling
Team
Collaborative research team with clinical and operational staff
About the Role
This position supports clinical trial execution by delivering medical care within protocol guidelines. The practitioner ensures participant safety and data integrity across multiple studies.
Work Schedule
Part-time hours with variable scheduling based on study needs, typically during daytime hours. Availability may include occasional weekends or extended shifts.
Physical Requirements
Ability to stand for prolonged periods, move between exam rooms, and assist participants with mobility. Manual dexterity for clinical equipment use is required.
Compliance and Training
Completion of GCP, HIPAA, and site-specific training is mandatory. Ongoing education and protocol-specific training will be provided.
Equal Opportunity Employer
We provide employment opportunities without regard to race, color, religion, sex, national origin, age, disability, or any other protected status.
Not available
