NewAmsterdam Pharma Corporation

NewAmsterdam Pharma Corporation

Executive Medical Director, Alzheimer’s Disease

Remote - USA, USA · Director

Sponsorship not specified$20k-$25kDetected 27 days ago
GCPData AnalysisStatisticsClinical TrialsClinical ResearchFDA RegulatoryResearchLeadershipCommunicationCollaborationPublic SpeakingRegulatory Affairs

About the role

  • Our robust scientific approach focuses on advancing a new era of life-saving treatments for lipid-related disorders.
  • Over the last decade it has become apparent that one of the major risk factors for Alzheimer's disease, Apolipoprotein E4, is closely associated with lipid dysregulation in the brain.
  • As such, the Executive Medical Director, Alzheimer's Disease is a critically important and visible member of the clinical development team.

Responsibilities

  • Lead the formulation and implementation of the Clinical Development Plan while taking into consideration the strategic objectives
  • Protocol design: lead the clinical trial design to ensure the design support the strategic objectives.
  • Support site and subject retention
  • Contribute to drafting and reviewing of clinical documents, manuscripts, presentations, and regulatory submissions

Requirements

  • Board-certified required, with specialty in Neurology
  • Working knowledge of US FDA and EMEA AD related regulations and guidelines.
  • Ability to travel approximately 20-25%
  • Travel as required both domestically and internationally for scientific meetings

Nice to have

  • M.D. degree: Completion of ACGME-accredited residency and fellowship strongly preferred
  • Physician licensure in at least one state strongly preferred if based in US

Compensation

  • Salary and Benefits:

Benefits

  • We offer a competitive base salary, annual bonus, and long-term incentives.
  • In addition, we provide a comprehensive benefits package, including health insurance, dental and vision coverage, term life and disability coverage, and retirement plans.
  • Work with CRO medical monitors and sites to review and respond to site queries related to protocols, such as eligibility criteria, adverse event questions, drug administration, etc.
  • Support the PV department in oversight of the medical & safety monitoring conducted by the CRO
  • Maintain up-to-date knowledge of relevant science, medical information, good clinical practices, and regulatory guidance

Equal opportunity

  • equal opportunity employer.

This listing is sourced directly from NewAmsterdam Pharma Corporation's careers page and normalized into a canonical job model.