Chief Medical Officer

Allorion Therapeutics

• $250K — $300K *
Pharmaceuticals & Biotech
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • MD with a strong clinical research background or MD/PhD with oncology experience
  • 15+ years of industry experience and 5+ in leading oncology clinical development
  • Experience in early-stage oncology clinical development and regulatory interactions
  • Ability to thrive in a small/medium size biotech environment
  • Excellent interpersonal and collaboration skills for a matrixed organization
  • Strong communication skills for effective information delivery
  • Strong organizational and planning skills for managing multiple projects

Responsibilities

  • Oversee clinical research, operations, data management, and regulatory functions
  • Lead drug development teams from IND to registration phases
  • Build and manage clinical development/project management teams
  • Formulate clinical strategies with cross-functional teams
  • Review and sign-off of all major clinical documents
  • Lead regulatory interactions and external scientific discussions
  • Provide strategic guidance for R&D and commercialization decisions

Benefits

  • Health, dental, and vision insurance
  • Retirement savings plans
  • Paid time off and holidays
  • Opportunities for professional development
  • Collaborative work culture in an innovative environment
Full Job Description
Natick, Massachusetts Position closed We seek a highly motivated and experienced leader as the Chief Medical Officer to advance Allorion's programs. The successful candidate will be a key member of the Allorion leadership team and responsible for ensuring the strategic planning and execution of clinical development within timelines and budgets and with high qualities. Responsibilities • Oversee multiple functions, including clinical research, clinical operations, data management, project management, and regulatory • Lead Allorion drug development project teams to define the approaches from IND, first-in-human to registration • Build clinic development/project management team(s) and be accountable for the successful execution of the clinical development strategies and plans, from global FIH to registrational studies • Work across a matrixed organization with Discovery Biology, Translational Medicine, DMPK/clinic pharm, Tox, and CMC to formulate the clinical development strategies • Be responsible for the final review and sign-off of all controlled clinical documents, including protocols, IBs, informed consent forms, as well as all major written deliverables • Lead the external forums, including regulatory interactions, scientific meetings, and partnership discussions • Provide strategic perspective and guidance to Allorion's R&D and commercialization for discussions and decisions from clinical development standpoints Required Skills • MD with strong clinical research background or MD/PhD with experience in oncology • 15+ years of industry experience with 5+ years in leading clinical development of oncology assets, with demonstrated track records in clinical development • Experience in oncology early-stage clinical development and regulatory interactions with health authorities • Ability to thrive in the highly entrepreneurial biotech environment, with experience in a small/medium size company • Excellent interpersonal skills and mindset of collaboration and teamwork, and the ability to function in a highly matrixed organization • Excellent communication skills, including presentation and writing skills, and the ability to convey information through written and verbal approaches effectively and efficiently • Organizing and planning skills in using time effectively, meeting project deadlines, and handling multiple assignments simultaneously Contact us

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