Mississippi Clinical Trials PI — Remote Oversight

Covalent Clinical Research; Mississippi; On-site; USD 85,000 - 120,000; Part time

Job summary

Covalent Clinical Research is looking for experienced Principal Investigators to lead clinical trials in Mississippi. This role focuses on scientific oversight, regulatory compliance, and participant safety, especially in underserved communities.

The ideal candidate will have a clinical license (MD, DO, NP, PA) and a commitment to health equity through inclusive research practices. Responsibilities include overseeing trial protocols and mentoring study staff.

Remote oversight may be possible, but candidates must be based in Mississippi or surrounding regions.

Qualifications

• Experience as Principal Investigator (PI) or Sub-Investigator (Sub-I) preferred.
• Strong knowledge of clinical trial regulations and documentation.
• Commitment to ethical research and advancing health equity.

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.
• Collaborate with sponsors, CROs, and Covalent’s central operations.

Skills

Clinical trial regulations knowledge

Communication skills

Leadership skills

Community engagement

Education

MD, DO, NP, PA, or equivalent clinical license

Job description

Covalent Clinical Research is looking for experienced Principal Investigators to lead clinical trials in Mississippi. This role focuses on scientific oversight, regulatory compliance, and participant safety, especially in underserved communities.

The ideal candidate will have a clinical license (MD, DO, NP, PA) and a commitment to health equity through inclusive research practices. Responsibilities include overseeing trial protocols and mentoring study staff.

Remote oversight may be possible, but candidates must be based in Mississippi or surrounding regions.