Senior Medical Director, Neuro-Oncology

SERVIER MONDE

5d • Hybrid

About The Position

With commercial stage products and a promising pipeline, we are a US-based affiliate of Servier Group, a unique global organization headquartered in France. Operating in more than 150 countries and governed by a non-profit foundation, we have multiple medicines approved in
oncology, & other disease states globally. Additionally, we have accelerated our investments with an ambition to further establish ourselves as innovators in the Oncology space. Over half of our research and development efforts are specifically focused on delivering significant advances in targeted therapies to treat patient communities with unmet needs. At Servier, you will join a highly skilled team dedicated to bringing the promise of tomorrow to the patients we serve.

Servier is seeking a Medical Director in the Oncology Late-Stage Clinical Development Team.

This role will provide medical leadership and expertise to ensure the successful design, implementation, and completion of clinical studies for oncology products in late-stage development, while adhering to regulatory requirements and company objectives. The initial focus will be on the clinical development of a leukemia asset with potential to work with other oncology assets in the pipeline.

Requirements

• Medical degree (M.D./D.O.) or equivalent required and specialization in Neuro-oncology or Medical oncology preferred with a minimum of three years of industry experience in clinical development, preferably with late-stage oncology clinical trials or a strong relevant academic background.
• Prior experience with clinical trial design, execution, and data analysis
• Excellent public speaking, writing, and communication skills
• Strong cross-functional leadership and collaboration skills
• Ability to work effectively in a fast-paced, dynamic, team-oriented environment

Responsibilities

• Manage the execution of clinical development activities for late-stage asset with a focus on clinical trial design, protocol writing and clinical trial implementation, ensuring compliance with regulatory requirements for registration
• Act as a Medical Monitor and provide medical monitoring oversight and guidance throughout phase 2-3 clinical trials while partnering with a cross-functional team
• Lead a cross-functional team spanning safety, clinical operations, pre-clinical, clinical pharmacology, and medical affairs, that strives to advance novel therapies from development to patients
• Drive analysis and interpretation of clinical trial data to inform decision-making and support regulatory submissions
• Prepare and review regulatory documents, including investigator brochures, safety reports, clinical study reports, briefing documents, and submission dossiers
• Present clinical trial design and results to internal and external stakeholders, including key opinion leaders, advisory boards, investigator meetings, regulatory agencies, and scientific conferences
• Develop and deliver scientific presentations, abstracts and manuscripts

Benefits

• Servier also offers a competitive and comprehensive benefits package that includes benefits such as medical, dental, vision, flexible time off (Servier provides unlimited sick time and flex time, and does not accrue time off), 401(k), life and disability insurance, recognition programs among other great benefits (all benefits are subject to eligibility requirements).
• Employees in this position are also eligible for Short-Term and Long-Term incentive programs.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Ph.D. or professional degree