Principal Investigator, MD/DO – Cardiology Clinical Trials

Hawthorne Health

. Accurately document findings and contribute to ongoing clinical trials, registries, or research protocols as applicable .

Posted 10/15/2026part-timeUnited StatesLead💰 $100 - $250 per hourWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical trials, ensuring compliance with ICH-GCP guidelines and FDA regulations, while effectively leading a research team and maintaining high standards of patient safety and ethical conduct.

Highest-signal resume keywords

MD with Clinical Research ExperienceLeadership in Clinical TrialsIn-Depth Knowledge of ICH-GCP GuidelinesStrong Verbal and Written Communication SkillsExceptional Organizational Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementPatient Assessment ReviewLaboratory Result InterpretationProtocol Deviation ManagementInvestigational Product Accountability

Soft Skills

Excellent Clinical JudgmentDecision-Making AbilitiesMeticulous Attention to DetailAbility to Prioritize Tasks

Tools & Technologies

Contract Research Organizations (CROs)Institutional Review Boards (IRBs)

Certifications & Qualifications

Current Unrestricted Medical LicenseBoard Certification in Cardiology

Industry Keywords

Good Clinical Practice (GCP)FDA RegulationsEthical ConductPatient SafetyClinical Research Protocols

About the role

Key responsibilities & impact

Accurately document findings and contribute to ongoing clinical trials, registries, or research protocols as applicable
Oversee and manage all aspects of clinical trials conducted at the research site, ensuring adherence to the study protocol, Good Clinical Practice (GCP), ICH guidelines, and all applicable regulatory requirements
Lead and supervise the clinical research team, including sub-investigators, study coordinators, and other site staff
Delegate study-related duties appropriately to qualified personnel and ensure proper training and oversight
Conduct remote review of patient assessments, including physical exams, medical histories, and eligibility screenings, to ensure appropriate participant enrollment
Review and interpret laboratory results, ECGs, and other diagnostic tests
Make critical medical decisions regarding participant care, adverse events, and protocol deviations
Ensure accurate, complete, and timely collection and documentation of all study data
Communicate effectively with sponsors, Contract Research Organizations (CROs), Institutional Review Boards (IRBs), and regulatory authorities
Manage investigational product accountability, storage, and administration according to protocol and with the help of the on-site IP team
Participate in site initiation visits, monitoring visits, audits, and inspections
Maintain continuous medical education and stay current with advancements in clinical research and relevant therapeutic areas
Attend on-site approximately 1–4 times per month for key visits, with additional remote oversight responsibilities of approximately 3–5 hours per week

Requirements

What you’ll need

Must be an MD with experience leading at least three sponsor initiated trials as a PI or Sub-I
Current, unrestricted medical license
Board certification in Cardiology preferred
Demonstrated in-depth knowledge of ICH-GCP guidelines, FDA regulations, and other relevant ethical and regulatory requirements for clinical research
Proven leadership and team management skills
Excellent clinical judgment and decision-making abilities
Strong verbal and written communication skills in English, with the ability to present complex information clearly and concisely
Exceptional organizational skills and meticulous attention to detail
Ability to manage multiple complex studies simultaneously and prioritize tasks effectively
Commitment to ethical conduct and patient safety

Benefits

Comp & perks

Flexible compensation adjusted based on experience and qualifications
Part-time schedule
Remote oversight work (approximately 3–5 hours per week)