Principal Investigator / Sub-Investigator - Cardiology Mississippi

Principal Investigator (Cardiology, PRN) Location: Diamondhead, MS Engagement Type: PRN / Contract (approximately 5–10 hours per week) Onsite Requirement: Yes Overview The Principal Investigator (PI) provides medical leadership and overall oversight for cardiology-focused clinical research studies conducted at the Diamondhead, MS site.

This PRN role ensures that all study activities are performed in compliance with ICH-GCP, FDA, and institutional standards, prioritizing participant safety, data integrity, and regulatory compliance.

The PI serves as the main point of contact for sponsors, CROs, and study monitors.

Key Responsibilities Lead and oversee all cardiology-related clinical trial activities at the site.

Evaluate and determine participant eligibility and safety throughout the study.

Review and approve study protocols, informed consent forms, and case report documentation.

Supervise sub-investigators, research coordinators, and clinical staff to ensure GCP compliance.

Oversee investigational product management, including drug accountability and storage.

Review and sign off on adverse event and serious adverse event (AE/SAE) reports.

Ensure all regulatory documentation and study files are inspection-ready.

Maintain ongoing communication with sponsors, IRBs, and study monitors.

Analyze study outcomes and contribute to final reports and publications.

Qualifications Doctor of Medicine (M.D.) or equivalent from an accredited institution.

Active, unrestricted Mississippi medical license.

Board certification in Cardiology or Internal Medicine (Cardiology focus) required/preferred.

Minimum 5 years of experience as a Principal Investigator or Sub-Investigator in clinical research.

Strong understanding of ICH-GCP, FDA regulations, and clinical research ethics.

Proven leadership in managing clinical teams and ensuring study compliance.

Excellent clinical judgment, organizational, and communication skills.

Schedule & Compensation PRN engagement (approx.

5–10 hours per week, variable by study phase). Compensation aligned with Fair Market Value (FMV) for investigator oversight in cardiology clinical research.

Sub-Investigator (Cardiology, PRN) Location: Diamondhead, MS Engagement Type: PRN / Contract (approximately 5–10 hours per week) Onsite Requirement: Yes Overview The Sub-Investigator (SI) supports the Principal Investigator in the conduct of cardiology clinical research trials at the Diamondhead site.

The SI performs delegated clinical and research duties, ensuring compliance with study protocols, ethical standards, and regulatory guidelines, under the direct supervision of the PI.

Key Responsibilities Conduct cardiology-related clinical assessments and patient study visits.

Assist the PI in participant screening, eligibility determination, and informed consent discussions.

Document patient data, adverse events, and concomitant medications in study records.

Perform ECGs, echocardiograms, and other cardiac assessments as required by the protocol.

Collaborate closely with the PI, study coordinators, and sponsor monitors.

Review study documentation for accuracy and completeness.

Ensure adherence to FDA, ICH-GCP, and institutional policies.

Qualifications Licensed MD, DO, NP, or PA in the state of Mississippi.

Experience in Cardiology or Internal Medicine preferred.

Prior experience as a Sub-Investigator or Clinical Research Physician strongly desired.

Good Clinical Practice (GCP) and Human Subjects Protection certification required.

Excellent attention to detail, clinical documentation, and patient interaction skills.

Schedule & Compensation PRN (as-needed) engagement — 5–10 hours per week on average.

FMV-based hourly or per-study compensation commensurate with experience.

Ref: #568-Clinical

Full-Time