Cardiologist - Clinical Research Investigator

ECN Operating LLC; Sun City (AZ); On-site; USD 150,000 - 250,000; Part time

Job summary

ECN Operating LLC is looking for a dedicated Physician – Cardiologist to join their team in Sun City, Arizona. This part-time position offers a unique opportunity to serve as a Principal Investigator in clinical trials while providing ongoing medical care to adult patients. Candidates must hold an MD or DO degree, have a valid medical license, and be Board Certified or Eligible in Cardiology. Responsibilities include managing patient eligibility and ensuring compliance with clinical protocols while collaborating with a research team.

Qualifications

• Must possess an MD or DO degree from an accredited medical school.
• Valid, unrestricted medical license in the state of employment required.
• Board Certified or Board Eligible (BC/BE) in Cardiology is necessary.
• Willingness to obtain GCP certification prior to start is required.
• Minimum of 1 year of experience in clinical practice is mandatory.

Responsibilities

• Serve as Principal Investigator or Sub-Investigator on clinical trials.
• Evaluate patient eligibility based on clinical protocols.
• Provide medical oversight and care for trial participants.
• Collaborate with Clinical Research Coordinators and Sponsors.
• Maintain clinical trial documentation in compliance with regulations.

Skills

Attention to detail

Interpersonal skills

Communication skills

Clinical trial management

Clinical practice

Education

MD or DO degree

Valid medical license

Board Certified or Board Eligible in Cardiology

GCP certification

Tools

Electronic Medical Records (EMRs)

Clinical Trial Management Systems (CTMS)

Job description

Elite Clinical Network (ECN) is seeking a dedicated and research-oriented Physician – Cardiologist to join our expanding team of clinical professionals. The ideal candidate will play a critical role in the conduct of clinical trials by serving as a Principal Investigator (PI) or Sub-Investigator, while continuing to provide high-quality medical care to adult patients within a clinical research setting. This is a part time/per diem position with a unique opportunity to contribute to the advancement of medicine through clinical studies.

Key Responsibilities

• Serve as a Principal Investigator or Sub-Investigator on multiple Phase I–IV clinical trials.
• Perform comprehensive physical exams and clinical assessments for protocol screening and enrollment.
• Evaluate patient eligibility based on inclusion/exclusion criteria of clinical protocols.
• Provide medical oversight for clinical trial participants, including safety assessments, adverse event evaluations, and ongoing care.
• Collaborate closely with Clinical Research Coordinators, Sponsors, and Monitors to ensure protocol compliance and data integrity.
• Review and sign off on source documents, case report forms (CRFs), and regulatory documentation.
• Maintain detailed and accurate clinical trial documentation in compliance with ICH‑GCP, FDA, and sponsor requirements.
• Participate in Site Initiation Visits (SIVs), Monitoring Visits, and Audits as needed.
• Manage chronic and acute conditions among study participants in alignment with standard care and protocol guidelines.
• Educate and counsel patients on study procedures, informed consent, and potential side effects.
• Support recruitment efforts and promote patient retention in trials.

Qualifications

• MD or DO degree from an accredited medical school.
• Valid, unrestricted medical license in the state of employment.
• Board Certified or Board Eligible (BC/BE) in Cardiology.
• BC/BE in Family Medicine or Geriatric Medicine will also be considered.
• Current Good Clinical Practice (GCP) certification or willingness to obtain prior to start.
• Minimum of 1 year of experience in clinical practice; prior clinical research experience preferred but not required.

Preferred Skills

• Familiarity with FDA, ICH‑GCP, and clinical trial protocols.
• Experience managing or participating in industry-sponsored clinical trials.
• Strong attention to detail and ability to document accurately.
• Excellent interpersonal and communication skills for patient interaction and sponsor collaboration.
• Ability to work collaboratively with a cross‑functional team in a fast‑paced research environment.
• Comfortable using electronic medical records (EMRs) and clinical trial management systems (CTMS).