Principal Investigator Jobs

Charlton Morris is proud to partner with a leading full-service CRO, who are currently seeking a Principal Investigator for their St. Pete site, who can fulfil their business needs and provide world class leadership to the team.

About Them

Our client is a full-service Clinical Research Organization (CRO) that provides comprehensive and integrated offerings in Early Phase, Late Phase, Respiratory, Dermatology, Consumer Research, Research Lab, IVRT, Biometrics, Pharmacovigilance & Medical Services, and Environmental Exposure Chambers (EECs).

They are headquartered in Ahmedabad and have expanded their domestic presence with 5 regional offices & international presence with offices in USA (Florida), Canada (Mississauga, Winnipeg & Scarborough) & Europe (Portugal).

Overview of Role

We are looking for a seasoned PI to direct and oversee all research activities and foster a culture of research integrity within their St. Petersburg FL location. This individual is responsible for fiscal and administrative management of research. Conduct research in an objective and unbiased manner in compliance with policies and regulations. While the PI may delegate responsibility for some project activity to others, the PI is ultimately responsible for compliance with all applicable regulations and policies and for ensuring a safe research environment, meaning one that is inclusive and free from any form of discrimination or harassment.

Key Expectations for the Role

• Responsible for the safety and well-being of the volunteer subjects
• Assure that all key research personnel have met training requirements.
• Coordinate with Business Development and Site to ensure that sponsored research activities are in accordance with all applicable regulations, policies, and procedures.
• Reviews and interprets clinical laboratory tests, ECGs, medical history data, and other clinical information regarding potential and enrolled study subjects to evaluate eligibility or ongoing
• Ensure optimal study conduct.
• Provide medical monitoring for clinical studies.
• Review and approve protocols, case report forms, informed consent forms, and other study documentation.
• Serve as Principal Investigator or Sub-Investigator on assigned clinical trials.
• Review and approve final study reports or other clinical documents.
• Acts as part of a multidisciplinary team to provide continuity of care to patients throughout various stages of treatment on protocol and follow-up.
• Review, prepare, and submit results for publication and register publication, as required by sponsor.
• Ensure appropriate resources for research conduct.

What you’ll bring:

To perform this job successfully, an individual must have:

• Bilingual skills preferred.
• Excellent organizational skills, detail oriented, efficient, and able to multi-task and prioritize effectively.
• Strong written and verbal communication skills
• Medical License within the State of Florida.
• Broad knowledge of general medicine
• A minimum of 3 or more years of experience in a clinical research position
• Strong analytical and problem-solving skills
• Excellent interpersonal skills.
• Medical Degree and broad-based post-graduate experience
• Medical board certification preferred

Full-Time On-site Position

This role is a full-time role within this company and qualifies for up to 80 hours of PTO as well a vacation time annually, in addition to a generous health and benefits package.

Why Them?

This company is on the cutting edge of clinical trials. If you are interested in being part of the next breakthrough in clinical trial research, then we are looking for you!