Head of R&D

Posted on: December 19, 2024

Anavex Life Sciences, a fast-growing biopharmaceutical company specializing in addressing neurodevelopmental and neurodegenerative conditions, is seeking an experienced, detail-oriented professional to take a hands-on lead as Head of R&D. Reporting to the CEO, this position calls for a professional that thrives in a start-up environment.

Key Responsibilities

  • Hands-on leadership of medical and clinical development activities, including but not limited to clinical development, medical affairs, regulatory affairs, and pharmacovigilance.
  • Develop strategies to support Anavex’s goals and objectives.
  • Ensure clinical trials are conducted to the highest ethical and scientific standards and follow relevant regulations and guidelines.
  • Manage and streamline the company’s medical affairs, regulatory affairs, and pharmacovigilance teams, ensuring effective communication and collaborative teamwork across all departments.
  • Establish, maintain, and leverage strategic relationships with key opinion leaders, regulatory authorities, and other relevant stakeholders.
  • Roll up your sleeves with other members of the company’s executive team, problem solve, and establish and manage the execution of strategic plans.

 

The position will be filled at a level commensurate with experience with a salary range of $250,000 – $400,000 per year.

Requirements

  • PhD/MD/PharmD with a background in neurology and/or CNS diseases preferred
  • Minimum of 15 years of experience in the pharmaceutical industry, with at least 5 years in a senior leadership role
  • Extensive experience in clinical development, including the design, execution, and analysis of clinical trials
  • Deep understanding of the regulatory environment for drug development, including FDA and EMA guidelines
  • Interest in accepting a hands-on leadership role in a rapidly evolving start-up environment
  • Track record of bringing new drugs to market, preferably in neurology or related therapeutic areas
  • Knowledge of drug safety and pharmacovigilance practices

Location

Flexible work arrangements may be possible.