Remix Therapeutics

Remix Therapeutics

Senior Medical Director, Clinical Development

Watertown, MA · Director

Sponsorship not specified$230k-$330kDetected 33 days ago
GCPICD-10Clinical TrialsFDA RegulatoryPharmacovigilanceLeadershipCommunicationCollaborationBiostatisticsRegulatory Affairs

About the role

  • This role is for a clinician ready to take on real medical ownership and help shape how REM-422 and future programs are developed.
  • Reporting directly to the Chief Medical Officer at our Watertown, MA headquarters, you will work alongside senior leadership at a pivotal moment in the company's clinical trajectory, with direct visibility into how key development decisions get made.
  • You will be a core contributor across a small, high-caliber cross-functional team where your judgment matters from day one.

Responsibilities

  • Author and revise clinical documents including protocol synopses, IB sections, ICFs, and CSR narratives
  • Support FDA and other agency meeting preparation
  • Collaborate with Clinical Operations on site selection, patient recruitment strategies, and trial execution
  • Partner with KOLs, CROs, and investigators
  • REM-422 is our lead program, currently in clinical evaluation for ACC and AML/HR-MDS, and it is at a critical inflection point.
  • Remix is building the team to bring this novel molecule forward for patients.

Requirements

  • 5+ years of oncology clinical development experience within a biotech or pharmaceutical organization
  • Working knowledge of ICH/GCP guidelines and FDA regulatory requirements
  • Strong scientific acumen with ability to engage deeply with translational data and biomarker-driven programs
  • Experience with rare solid tumors, ACC, or head and neck oncology
  • Experience on biomarker-heavy or genomically-selected programs
  • Familiarity with RNA or spliceosome biology
  • MD or equivalent medical degree
  • Hands-on experience as a medical monitor or clinical study physician, including SAE review and site oversight
  • Familiarity with early-phase (Phase 1/1b) oncology trial design and execution
  • Excellent written and verbal communication; able to author clinical documents and synthesize complex data for varied audiences
  • Exposure to hematologic malignancies (AML, MDS)

Compensation

  • This range reflects the expected base salary for this position, plus bonus, equity, and benefits as applicable.
  • Actual salaries may vary based on factors, such as skill, experience, and qualification for the role.
  • $230,000-$ 330,000 USD

Benefits

  • Clinical Trial Execution & Medical Monitoring
  • Serve as physician lead and medical monitor for REM-422 clinical studies, with direct accountability for patient safety, protocol adherence, and scientific and ethical rigor
  • Respond to site medical queries, review eligibility exceptions, and support investigators on protocol requirements and deviation management
  • contribute medical sections to regulatory filings and briefing documents
  • provide medical input on vendor deliverables, data collection tools, and medical coding

Company info

  • We are seeking someone with 5+ years of industry experience in oncology drug development and looking to grow as Remix scales.
  • At Remix Therapeutics, we intend to change that.
  • We are a clinical-stage biopharmaceutical company that has pioneered a new class of small molecule medicines targeting the RNA splicing machinery - correcting the disease-causing errors that drive ACC and other serious conditions at their source.

This listing is sourced directly from Remix Therapeutics's careers page and normalized into a canonical job model.