Principal Investigator (PI) Clinical Research

Location: Mississippi-based sites (remote oversight possible)
Type: Contract (1099)
Reports to: Strategic Lead, Covalent Clinical Research

Role Summary:

Covalent Clinical Research is seeking experienced, community-rooted Principal Investigators to lead clinical trials across Mississippi. PIs will provide scientific oversight, ensure regulatory compliance, and uphold participant safety—especially in underserved and rural communities. This role is ideal for clinicians committed to advancing health equity through inclusive, community-engaged research.

Key Responsibilities:

• Oversee protocol execution and participant safety across assigned trials
• Ensure compliance with GCP, FDA, IRB, and sponsor requirements
• Supervise and mentor study staff; delegate responsibilities appropriately
• Review and approve protocols, informed consent forms, and amendments
• Maintain accurate source documentation and regulatory files
• Collaborate with sponsors, CROs, and Covalent’s central operations
• Support inclusive recruitment strategies and community engagement

Qualifications:

• MD, DO, NP, PA, or equivalent clinical license
• Prior experience as PI or Sub-I preferred
• Strong knowledge of clinical trial regulations and documentation
• Commitment to ethical research and health equity
• Excellent communication and leadership skills

Please note: Only candidates based in Mississippi or surrounding regions will be considered. This role is not eligible for US Visa Sponsorship.