Nephrologist - Clinical Research Role | Flexible Schedule (Denver, CO)

Benefits

Qualifications

• •Clinical Research Physician-Nephrologist Job Type: Full-Time / Part-Time / ContractLocation: Multiple (Denver, CO & Illinois)Compensation: based on specialty, experience, and contract type.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
• •RequirementsMD or DO degree with active, unrestricted U.S
• •Board certification in Dermatology or one of the listed specialties
• •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
• •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
• •5 more items(s)

Responsibilities

• •Specialties of InterestDermatology (high priority)CardiologyEndocrinologyGastroenterologyHematologyInfectious DiseaseInternal MedicineNephrologyNeurologyOncologyPulmonologyRheumatologySurgery (General & Subspecialties: Orthopedic, Cardiothoracic, etc.)Urology Key ResponsibilitiesServe 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
• •5 more items(s)