Cardiology Physician

ProTouch Staffing; Denver (CO); On-site; USD 120,000 - 210,000; Full time

Benefits offered by this job

Flexible scheduling

Opportunities in cutting-edge clinical

Professional growth in investigatore

Job summary

ProTouch Staffing is seeking board-certified physicians to serve as Clinical Research Cardiologists across multiple specialties. This role offers flexibility with part-time or full-time options, and opportunities to lead clinical trials while maintaining patient safety and high ethical standards.

Positions involve PI/Sub-I responsibilities, screenings, evaluations, and collaboration with sponsors, CROs, and IRBs. Active U.S.

Qualifications

• MD or DO degree with active, unrestricted U.S. medical license (CO and/or IL preferred).
• Board certification in Dermatology or listed specialties.
• DEA license and BLS/ACLS certification preferred.
• Prior experience in clinical research strongly preferred (training available for motivated candidates).
• Proficiency with EHR, EDC, CTMS, and medical documentation systems.

Responsibilities

• Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) on clinical trials.
• Conduct medical screenings, physical examinations, and specialty-specific evaluations for study participants.
• Provide medical oversight and ensure patient safety throughout all trial phases.
• Monitor, document, and report adverse events (AEs/SAEs) per protocol and regulatory standards.
• Collaborate with study coordinators, research staff, sponsors, CROs, and IRBs to ensure compliance and data quality.
• Participate in site initiation visits, monitoring visits, audits, and investigator meetings.
• Contribute to protocol feasibility reviews, recruitment strategies, and study design discussions.
• Maintain compliance with GCP, FDA regulations, and institutional guidelines.
• Stay updated on clinical research practices and therapeutic advancements.

Skills

Clinical Research

Interdisciplinary Collaboration

Communication Skills

Regulatory Knowledge

Education

MD/DO

Tools

EHR

EDC

CTMS

Job description

Clinical Research Physician-Cardiologist

Job Type: Full-Time / Part-Time / Contract

Location: Multiple (Denver, CO & Illinois)

Schedule: Flexible Part-Time (0-8 hours/week) or Full-Time options

Job Summary

We are seeking board-certified physicians across multiple specialties to serve as Clinical Research Cardiologist. This is an excellent opportunity for physicians passionate about advancing medicine through research while maintaining a flexible schedule.

Specialties of Interest

• Dermatology (high priority)
• Cardiology
• Endocrinology
• Gastroenterology
• Hematology
• Infectious Disease
• Internal Medicine
• Nephrology
• Neurology
• Oncology
• Pulmonology
• Rheumatology
• Surgery (General & Subspecialties: Orthopedic, Cardiothoracic, etc.)
• Urology

Key Responsibilities

• Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) on clinical trials.
• Conduct medical screenings, physical examinations, and specialty-specific evaluations for study participants.
• Provide medical oversight and ensure patient safety throughout all trial phases.
• Monitor, document, and report adverse events (AEs/SAEs) per protocol and regulatory standards.
• Collaborate with study coordinators, research staff, sponsors, CROs, and IRBs to ensure compliance and data quality.
• Participate in site initiation visits, monitoring visits, audits, and investigator meetings.
• Contribute to protocol feasibility reviews, recruitment strategies, and study design discussions.
• Maintain compliance with GCP, FDA regulations, and institutional guidelines.
• Stay updated on clinical research practices and therapeutic advancements.

Requirements

• MD or DO degree with active, unrestricted U.S. medical license (CO and/or IL preferred).
• Board certification in Dermatology or one of the listed specialties.
• DEA license and BLS/ACLS certification preferred.
• Prior experience in clinical research strongly preferred (training available for motivated candidates).
• Proficiency with EHR, EDC, CTMS, and medical documentation systems.
• Strong communication and interpersonal skills; ability to work in a multidisciplinary, fast-paced environment.
• Commitment to ethical research and patient-centered care.

Compensation & Benefits

• Flexible scheduling (0-8 hours/week part-time or full-time).
• Opportunity to participate in cutting-edge clinical trials across multiple therapeutic areas.
• Professional growth in research leadership and investigator experience.