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Lead Clinical Research Physician

Massachusetts Clinical Research Institute
Boston
Salary Estimate
USD 220.000 – USD 260.000
Live Update
30 Mei 2026
Deadline
30 Mei 2027

Job Description

Are you a visionary medical professional seeking to push the boundaries of modern medicine? Massachusetts Clinical Research Institute is searching for a Lead Clinical Research Physician to pioneer groundbreaking clinical trials in Boston, MA.

In this high-impact role, you will oversee phase II and III clinical development programs, bridging the gap between innovative laboratory science and life-saving patient therapies. You will collaborate with elite global pharmaceutical partners and lead a world-class team of clinical researchers in a state-of-the-art environment.

We offer a premium compensation package, including comprehensive executive benefits, performance-driven bonuses, and dedicated funding for continuous academic and professional research pursuits.

Responsibilities

  • Serve as the Principal Investigator or Medical Monitor for multiple high-priority phase II and III oncology and immunology clinical trials.
  • Provide expert clinical oversight to ensure absolute patient safety, data integrity, and strict protocol adherence.
  • Collaborate with global drug development teams to design clinical study protocols, investigator brochures, and clinical study reports.
  • Analyze, interpret, and present complex clinical trial data directly to regulatory bodies, including the FDA and EMA.
  • Mentor and lead a dedicated team of clinical research coordinators, sub-investigators, and clinical research nurses.
  • Establish and nurture strategic partnerships with key opinion leaders (KOLs) and global academic medical centers.

Qualifications

  • Doctor of Medicine (MD) or Doctor of Osteopathic Medicine (DO) degree with an active, unrestricted US medical license.
  • Board Certification in Oncology, Hematology, Immunology, or a highly related therapeutic specialty.
  • Minimum of 5 years of direct clinical trial leadership experience within the pharmaceutical, biotech, or academic CRO industries.
  • Expert-level knowledge of Good Clinical Practice (GCP), ICH guidelines, and FDA/EMA clinical trial regulations.
  • Proven track record of successful scientific contributions to IND, NDA, or BLA regulatory submissions.
  • Outstanding communicative presence with a history of peer-reviewed publications and presentations at major medical congresses.

Required Skills

Clinical Trials Oncology Medical Monitoring FDA Regulations GCP ICH Guidelines Drug Development Medical Research Leadership NDA/BLA Submissions

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