Job Description: Sub-investigator in Clinical Research
We are seeking a detail-oriented and collaborative Sub-Investigator to support clinical trials at our research site. The Sub-Investigator will work closely with the Principal Investigator (PI) to ensure studies are conducted safely, ethically, and in compliance with protocols, Good Clinical Practice (GCP), and regulatory guidelines.
Key Responsibilities:
- Assist the PI in overseeing clinical trial activities, including participant safety and protocol adherence.
- Conduct medical evaluations, physical exams, and review participant lab results.
- Address and document adverse events and ensure appropriate follow-up.
- Collaborate with research staff, sponsors, and monitors to ensure smooth trial execution.
- Review and maintain study documentation, including source documents and case report forms (CRFs).
- Provide input during site visits and audits as needed.
Qualifications:
- Advanced healthcare degree (e.g., NP, PA) or Medical degree (MD, DO, or equivalent)
- Clinical research experience preferred.
- Strong knowledge of GCP and regulatory requirements.
- Excellent organizational and communication skills.
