Job detail

Principal Investigator (MD/DO)

ObjectiveHealth

#FDA Regulations #E-Verify #SOPs #Clinical Research #Principal Investigator #GCP #Family Medicine #Board Certified #MD

Quick overview

The Principal Investigator will serve as the lead for assigned clinical trials, ensuring overall study oversight and enforcing strict compliance with protocols while always prioritizing subject safety. This role involves conducting and documenting medical assessments and providing continuous medical oversight throughout the trial lifecycle.

Requirements summary

Candidates must possess an active MD or DO license in Alabama and be board-certified in Internal Medicine or Family Medicine. Prior clinical research experience is preferred, and strong ethical standards, attention to detail, and excellent communication skills are essential.

postgraduate degreeAttention To DetailInterpersonal SkillsCommunicationCollaborationPhysical ExaminationsMedical OversightGCPEthical StandardsMedical AssessmentsClinical TrialsProtocol ComplianceFDA RegulationsICH GuidelinesInternal SOPsSubject Safety

Job description

Description Principal Investigator - Part-Time, Flexible Days ObjectiveHealth is seeking a board-certified MD or DO to serve as a Part-Time Principal Investigator at our Birmingham, AL research site. This is a unique opportunity for a physician in Internal Medicine or Family Medicine to contribute to innovative clinical research while maintaining a flexible schedule.

ObjectiveHealth is a clinical research company transforming how research is conducted at the point of care. Using our proprietary technology, we aim to: Increase patient access to research trials within our communities Provide physicians with enhanced care options for current patients Deliver superior clinical research enrollment metrics to Pharma sponsors All with the ultimate goal of Improving Patient Outcomes at the Point of Care. We want you to join us in doing just that.

Key Responsibilities

Serve as the Principal Investigator for assigned clinical trials, ensuring overall study oversight. Oversee and enforce compliance with study protocols while prioritizing subject safety at all times. Conduct and document physical examinations and medical assessments in accordance with research protocol requirements. Provide continuous medical oversight throughout all phases of the clinical trial lifecycle. Collaborate effectively with study coordinators, site staff, and other research team members to ensure smooth study execution. Participate in sponsor meetings, site initiation visits, monitoring visits, and audits as needed. Maintain strict compliance with GCP, ICH guidelines, FDA regulations, and internal SOPs.

Qualifications

MD or DO with a valid and active medical license in the state of Alabama with no history of license suspension or disbarment. Board certification in Internal Medicine or Family Medicine (additional specialty certifications are welcome). Prior clinical research experience is preferred but not required. Strong attention to detail and a demonstrated commitment to high ethical standards. Excellent communication and interpersonal skills, with the ability to collaborate effectively in a team-based environment.

Requirements

This job requires legal authorization to work in the US. We are not currently accepting work visas. ObjectiveHealth is an EEO Employer and an E-Verify participant