Medical Director/Medical Monitor Job at Vivid Resourcing, Boston, MA

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  • Vivid Resourcing
  • Boston, MA

Job Description

Job Description

Medical Director/Medical Monitor

Location: Boston, MA (Hybrid)

We are seeking an experienced Medical Director (Medical Monitor) to provide strategic and hands-on medical leadership to help drive the clinical development.

Some of the responsibilities include:

  • Supervise clinical trials, ensuring SOPs, GCPs and following regulatory requirements.
  • Design, implement clinical trials in the oncology space based on ICH-GCP and research guidelines.
  • Serve as Medical Monitor for oncology clinical trials, providing medical oversight and ensuring patient safety.
  • Review and assess SAEs, AESIs, and safety trends, partnering with Pharmacovigilance on signal detection and benefit–risk evaluation.
  • Provide medical input into protocol design, dose escalation decisions, and safety monitoring plans.
  • Contribute to clinical and regulatory documents (protocols, IBs, ICFs, CSRs) and support health authority interactions.
  • Collaborate cross-functionally with Clinical Operations, Regulatory Affairs, Biometrics, and Translational Medicine.
  • Engage with investigators, KOLs, and study sites to ensure high-quality trial execution and scientific alignment.

Requirements:

  • MD or DO (or international equivalent) with board certification or eligibility.
  • 4+ years of clinical trial experience in oncology/hematology, including medical monitoring responsibilities.
  • Strong understanding of oncology drug development, safety assessment, and global regulatory requirements.
  • Experience reviewing and managing SAEs, DLTs, and safety narratives.
  • Excellent communication skills with the ability to engage internal teams, investigators, and regulators.
  • Prior experience in biotech or emerging pharmaceutical companies.
  • Good communication with internal and external partners/stakeholders.

Offer:

  • Competitive salary ($200-300k)
  • Professional development and potential for upward career growth.
  • Impact in shaping regulatory strategy.

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