Clinical Research Physician - Internal Medicine; Part time

Accel Research Sites

Newton, MAPart-timePosted Apr 30, 2026

Behavioral Health Market Context

Latest national behavioral health workforce report (2026-W21)Massachusetts behavioral health workforce newsBrowse all behavioral health workforce news
Apply Nowvia Learn4Good

Benefits

Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hireMedical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered#J-18808-Ljbffr

Qualifications

  • •Minimum Qualifications: MD or DO degree, an active physician license (in good standing) in the state of practice for this role
  • •Board certification in area of specialty required
  • •Clinical skills and clinical procedures based on area of specialty
  • •Proficiency with computer applications such as MS Office, electronic health records, and web applications, and the ability to type proficiently (40+ wpm)
  • •Must possess strong organizational skills, attention to detail, and math proficiency
  • •Well-developed written and verbal communication skills
  • •3 more items(s)

Responsibilities

  • •Clinical Research Physician - Internal Medicine (Part time - 16-24 hrs/week)
  • •The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes
  • •Working with a local and central team drives clinical oversight and the quality of the assigned studies at the site
  • •Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes
  • •Overall site leadership with a focus on enhancing efficiencies, patient safety and protocol/GCP /regulatory compliance
  • •Evaluates and assesses participants to ensure only eligible participants enroll into the trials
  • •Participates and engages in successful delivery and retention of study participants
  • •Interacts positively and collaboratively with sponsors, clients and team members
  • •Practices attention to detail in recording data and participant information, following protocol guidelines and GCPs
  • •Actively involved in protocol training for staff
  • •Participate in Investigator Meetings (IMs), and continuing education activities in order to maintain current knowledge of recruitment affairs and issues
  • •Perform other duties as assigned, requested, or required based on the needs of the participants, protocols and/or company
  • •9 more items(s)
Apply for this Position

More Jobs