Physician – Internal Medicine

Position Overview

Position Overview Elite Clinical Network ECN is seeking a dedicated and research oriented Physician Internal Medicine 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 timeper diem position with a unique opportunity to contribute to the advancement of medicine through clinical studies

Key Responsibilities

• Serve as Principal Investigator or Sub Investigator on multiple Phase IIV clinical trials
• Perform comprehensive physical exams and clinical assessments for protocol screening and enrollment
• Evaluate patient eligibility based on inclusionexclusion 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 BCBE in Internal Medicine
• BCBE 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
• DEA license preferred

Pay

Pay 150 200hr