Medical Doctor - Cardiologist Job at Elite Clinical Network, Tucson, AZ

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  • Elite Clinical Network
  • Tucson, AZ

Job Description

Position Summary:

We are seeking a board-certified Cardiologist with a strong interest or background in clinical research to join our multidisciplinary team. The ideal candidate will play a central role in designing, conducting, and overseeing clinical trials related to cardiovascular disease, working collaboratively with research staff, sponsors, and regulatory bodies. This position offers a unique opportunity to contribute to advancements in cardiology through evidence-based investigation while maintaining limited patient care responsibilities.

Key Responsibilities:

  • Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) on clinical trials in cardiology.
  • Provide clinical oversight and ensure protocol adherence in all stages of trial execution.
  • Screen and assess patient eligibility for participation in clinical studies.
  • Monitor and evaluate safety and efficacy outcomes, including adverse event reporting.
  • Collaborate with research coordinators, nurses, and regulatory personnel to ensure compliance with Good Clinical Practice (GCP) and FDA guidelines.
  • Assist in the development of study protocols and contribute to scientific publications and presentations.
  • Maintain accurate and timely documentation of all research-related activities.
  • Liaise with sponsors, Contract Research Organizations (CROs), and institutional review boards (IRBs).
  • Provide medical guidance and interpretation of trial results in collaboration with biostatisticians and research analysts.

Qualifications:

  • MD or DO degree with board certification in Cardiology.
  • Valid medical license in Arizona
  • Prior experience in clinical research or trials preferred (e.g., GCP certification, investigator experience).
  • Strong analytical, communication, and organizational skills.
  • Passion for advancing cardiovascular medicine through research.

Preferred Skills:

  • Experience with electronic data capture systems and clinical trial management software.
  • Knowledge of regulatory frameworks (FDA, ICH-GCP, IRB processes).
  • Academic or industry experience in cardiovascular outcomes research is a plus.

Job Type : Part-time

Expected hours : No less than 20 per week

Job Tags

Contract work, Part time,

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