Cardiology Physician

ProTouch Staffing; Greenwich (CT); On-site; USD 138,000 - 344,000; Part time

Benefits offered by this job

Flexible schedule

Part-time opportunities

Competitive hourly rate

Job summary

ProTouch Staffing is seeking a board-certified Cardiologist to join our Greenwich, CT clinical research site as a part-time PI or Sub-I. The role involves overseeing clinical trial activities across Phases I–IV with a focus on patient safety and protocol compliance.

The position offers an 8-hour-per-week schedule, flexibility, and opportunities to contribute to groundbreaking medical research while maintaining clinical expertise.

Qualifications

• MD or DO with active Connecticut medical license.
• Board-certified in Cardiology.
• DEA license and BLS/ACLS certification.

Responsibilities

• Serve as PI or Sub-I across clinical trials.
• Conduct screenings, assessments, and exams.
• Ensure safety and protocol adherence per ICH-GCP and FDA.
• Collaborate with staff for documentation and trial execution.
• Monitor AEs/SAEs and maintain EHR/EDC compliance.
• Engage with sponsors, CROs, monitors, and IRBs.

Skills

Strong communication

Interpersonal skills

Collaborative mindset

Education

MD/DO

Tools

EHR systems

EDC

CTMS

Job description

Clinical Research Physician (Cardiologist) – Greenwich, CT

Schedule: Flexible Part-Time (8 hours per week)

About the Role

We are seeking board-certified Cardiologist to join our Greenwich, CT clinical research site. This part-time position offers physicians the opportunity to contribute to groundbreaking medical research while maintaining a flexible schedule. You will serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I), overseeing clinical trial activities and ensuring the highest standards of patient safety and protocol compliance across Phase I-IV studies.

Key Responsibilities

• Serve as PI or Sub-I across clinical trials in diverse therapeutic areas.
• Conduct medical screenings, specialty assessments, and physical examinations.
• Ensure participant safety and protocol adherence in compliance with ICH-GCP, FDA, and regulatory standards.
• Collaborate with coordinators, nurses, and research staff for accurate documentation and trial execution.
• Document patient interactions, monitor adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems.
• Engage with sponsors, CROs, monitors, and IRBs to support trial success.
• Participate in site initiation visits, monitoring visits, and audits.
• Provide medical expertise during feasibility reviews, recruitment strategies, and study design discussions.
• Stay updated on clinical research regulations and advances in investigational therapies.

Qualifications

• M.D. or D.O. with an active, unrestricted Connecticut medical license.
• Board-certified in Cardiology.
• Valid DEA license and current BLS/ACLS certification.
• Prior clinical research experience preferred (training available).
• Proficiency with EHR systems and clinical trial platforms (EDC, CTMS).
• Strong communication and interpersonal skills with a collaborative mindset.
• Commitment to ethical, patient-centered research.

Compensation & Benefits

Competitive hourly rate: $100 – $250 based on specialty and experience. Highly flexible, part-time schedule (ideal for supplemental income or work-life balance). Gain or expand experience in clinical research. Contribute to the advancement of medical innovation and patient care.