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Amylyx

Senior Vice President, Clinical Development

RemoteUnited States only· except United States, AK, Azerbaijan +3 more
Published
Experience
C-Level
Employment
Full-time
Company size
Mid-size
$416k–$468k/yr
Check eligibility

Open to US only · except US, AK, AZ, HI, MI, TN. Set where you work from to check your eligibility.

No BS summary

MD or MD/PhD with 15+ years in biotech/pharma clinical development, specifically in rare diseases. Must have led teams and have experience with BLA/NDA/MAA submissions and commercialization support. Requires strong leadership, regulatory knowledge, and communication skills. Remote within the US, with travel to Cambridge, MA.

Required languages

English

What you'll do

  • Provide strategic direction and technical leadership to the clinical development team, including clinical-regulatory development planning, clinical trial design, implementation and execution, clinical data analysis and management, and clinical competitive intelligence.
  • Participate in various business development evaluations, as applicable.
  • Provide strategic leadership for the clinical and medical aspects for the various programs and work closely with a cross-functional team to align the clinical development plan with the overall development strategy of the relevant products.
  • Oversee the clinical development of multiple product candidates that represent different modalities and are at different stages of development from first in human to pivotal trials.
  • Develop and implement comprehensive clinical development strategies aligned with Amylyx's mission and business objectives.
  • Lead and mentor a multidisciplinary team of medical directors, pharmacologists, and clinical development scientists, fostering a culture of collaboration and excellence.
  • Oversee the design, execution, and analysis of clinical trials, ensuring adherence to timelines, budgets, and regulatory requirements.
  • Collaborate with regulatory affairs to develop and execute strategies for regulatory submissions and interactions with health authorities.
  • Establish and maintain relationships with key opinion leaders, clinical investigators, and external partners to support clinical programs.
  • Develop and manage the clinical development budget, ensuring optimal resource allocation and fiscal responsibility.

What they require

  • MD or MD/PhD with specialization in Neurology or Endocrinology preferred.
  • Minimum of 15 years in clinical development within the biotechnology or pharmaceutical industry, with significant experience leading teams in rare disease drug development.
  • Successful BLA/NDA/MAA submission(s) and clinical/medical support of product commercialization preferred.
  • Proven ability to lead cross-functional teams, foster cross-functional collaboration and manage multiple projects in a fast-paced environment.
  • In-depth understanding of global regulatory requirements and experience with regulatory interactions and submissions.
  • Excellent verbal and written communication skills, with the ability to effectively present complex information to diverse audiences.
  • You will be expected to travel to our corporate location in Cambridge, MA several times a year and attend other company-related events as necessary and requested.
  • You must have access to work in setting which enables meeting all requirements of the role (including privacy, reliable internet access, phone, ability to video conference, etc.) at your remote location.

Benefits

  • health insurance coverage
  • state tax regulations

Amylyx is a clinical-stage company currently focused on post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS).

🇬🇧 United KingdomBiotechStartupamylyx.com/
$416k–$468k/yr