Medical Director

Allorion Therapeutics

• $210K — $250K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • M.D. degree required
  • 5+ years of industry experience in autoimmune and oncology drug development
  • Strong interpersonal, verbal, and written communication skills
  • Effective public speaking abilities
  • Fluency in English, both oral and written

Responsibilities

  • Oversee autoimmune or oncology drug development to ensure successful clinical trials
  • Lead pathology and biomarker group for patient selection strategies and biomarker development
  • Provide medical and scientific leadership to cross-functional teams on anti-neoplastic agents
  • Engage with global regulatory bodies like FDA and EMA on product development
  • Develop key documentation for clinical studies and regulatory submissions
  • Collaborate with external vendors for clinical study implementation
  • Serve as a medical and scientific expert for drug development design and execution
Full Job Description
Natick, Massachusetts

Position closed

We seek a talented Medical Director or Senior Medical Director who will be responsible for providing leadership and establishing strategy and implementing clinical drug developments.

Responsibilities

  • Oversee autoimmune or oncology drug development for successful implementation and conduct of clinical trials including early phase investigations and registration trials
  • Lead pathology and biomarker group for informing patient selection strategies and biomarker development locally and internationally
  • Provide medical and scientific leadership for internal cross-functional team members for development of anti-neoplastic agents including discovery scientists, medical scientists, biostatisticians, and pharmacokineticists
  • Interact with global regulatory bodies including the FDA and EMA to accomplish tasks related to autoimmune and oncology product development and collaborate with internal regulatory experts and oversee the clinical research plans and sections for Investigational new Drug applications (INDs) and New Drug Applications (NDAs)
  • Facilitate the development of key internal and external documents pertaining to product development including clinical study protocol, informed consents, CRFs, CSR, meeting abstracts and scientific journal publications
  • Collaborate with external vendors, such as CROs, external imaging and laboratory resources, for successful implementation and conduct of early phase and registration global clinical studies
  • Serve as a source for medical and scientific expertise in autoimmune or oncology for outlining design strategy and execution for drug development


Required Skills

  • M.D. degree
  • 5+ years of industry experience in autoimmune and oncology drug development
  • Strong interpersonal, verbal, and written communication skills
  • Strong public speaking skills
  • Oral and written proficiency in English


Contact us

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