Anavex

Head of Research & Development

10007, New York, NY, United States

Onsite
Full-time
9 months ago
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Summary

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

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