Principal Investigator (Part-Time) – Clinical Trial Investigator Position Available In Hinds, Mississippi

Principal Investigator (Part-Time) – Clinical Trial Investigator Covalent Clinical Research Jackson, MS Job Details Part-time Up to $300 an hour 1 day ago Qualifications Responsible conduct of research Medicine Clinical research Doctoral degree

BC/BE HIPAA

No experience needed Clinical trial projects Patient care Clinical trials Good Clinical Practice Senior level Communication skills Healthcare research FDA regulations Under 1 year

Full Job Description Overview:

We are seeking a dedicated, board-certified Medical Doctor to serve as Principal Investigator (PI) for our newly established clinical research site in Jackson, Mississippi —a research-naïve, underserved region with untapped potential to contribute to the future of healthcare through clinical trials. As a PI, you will lead ethically responsible clinical investigations that support cutting-edge research while providing access to innovative therapies for patients who’ve historically lacked exposure to clinical studies. This role offers a unique opportunity to be at the forefront of building a research culture in an area where clinical trials have rarely, if ever, been conducted. This is a part-time role with compensation based on a revenue-sharing model tied to the number of patients enrolled, net after operational costs . It’s ideal for a physician who wants to impact their community while expanding their influence in the growing clinical research industry.

Primary Responsibilities:

Serve as the responsible medical lead for the ethical, safe, and compliant conduct of assigned clinical trials Oversee and ensure the protection of patient rights and safety throughout study participation Assess and confirm eligibility of potential study participants according to protocol inclusion/exclusion criteria Obtain and/or oversee informed consent process and ensure accurate documentation Conduct and document study visits including physical exams, diagnostics, safety reviews, and protocol-specific assessments Review all safety data (labs, adverse events, medications) and apply medical judgment in real time Ensure accuracy and timely completion of eCRFs, protocol deviations, adverse event reports, and other key study documentation Manage investigational product (IP) handling, storage, accountability, and return as per protocol Liaise with IRBs, Sponsors, CROs, and regulatory agencies as needed for monitoring, audits, and inspections Attend Investigator Meetings and training as required by sponsors Work closely with Sub-Investigators, CRCs, and research staff to uphold study protocol compliance Serve as an ambassador for research in the community, helping foster trust and education around clinical trials

Knowledge, Skills & Qualifications:

MD or DO with current license to practice in Mississippi Board Certified in any specialty Prior experience as a Principal or Sub-Investigator preferred but not required—training and mentorship available Understanding of

GCP, FDA

regulations, ICH guidelines, and HIPAA compliance Excellent clinical judgment and decision-making skills Strong written and verbal communication and documentation skills Passion for health equity, patient access, and advancing medical knowledge in clinical research Why Join Us? At Covalent Clinical Research , we believe that success in research starts with access . Located in a region where research has historically been out of reach, our mission is to bring clinical trials to those who’ve been left out of innovation. This role offers you a chance to be the first Principal Investigator in a transformative movement—one that combines science, equity, and local impact. We are an equal opportunity employer committed to diversity, equity, and inclusion across all levels of our organization.

Company Name:

Covalent Clinical Research, LLC Location:

Jackson, MS Website:

www.covalentclinicalresearch.com Contact for

Inquiries:

Join us in advancing medical research and improving patient outcomes through effective clinical trial management. We look forward to your application!

Job Type:

Part-time Pay:

Up to $300.00 per hour Expected hours: 15 – 20 per week

Medical Specialty:

Cardiology Dermatology Endocrinology Gastroenterology Hematology Infectious Disease Nephrology Neurology Oncology Rheumatology Transplant Surgery Urology Ability to

Commute:

Jackson, MS 39205 (Required) Ability to

Relocate:

Jackson, MS 39205: Relocate before starting work (Required)

Work Location:

In person