Associate Medical Director, Clinical Development Rare Movement Disorders

About This Role The Rare Neurology Development Unit (RNDU) at Biogen is accountable for developing ground-breaking therapies in Spinal Muscular Atrophy (SMA), Amyotrophic Lateral Sclerosis (ALS), and Rare Movement Disorders (RMD) e.g., Friedreich Ataxia (FA) or Huntington’s disease. As a member of the RMD and FA team, the Associate Medical Director will support early and/or late-stage program(s). This role will ensure the successful execution of clinical trials, in line with the strategic plan and assist the team in achieving innovative clinical trial designs, endpoints, biomarkers and in regulatory interactions. In this role you will report to the Director, FA Clinical Development. What You’ll Do Support the development and oversight of study protocols and amendments, clinical study reports, training documents, and other clinical and regulatory documents. Monitor, review, and interpret safety and efficacy data of assigned clinical trials. Represent clinical development on cross-functional study management teams to ensure successful design and execution of clinical studies and achievement of study quality metrics. Contribute to regulatory submissions and interactions, publications, and presentations. Contribute to the preparation and execution of investigator and advisory board meetings in partnership with project teams and stakeholders. Remain up to date on regulations and guidelines for the therapeutic area.

You are a driven team member who can think globally about advancing therapeutics and work effectively with cross-functional partners across multiple studies within the rare neurology / FA space. You have a strong understanding of clinical trial design, execution, and interpretation of clinical trial results and contribute to regulatory submissions and interactions. You are effective in a highly matrixed environment and possess expert knowledge of scientific medical and regulatory information for publications and presentations.

MD, Ph.D., and/or PharmD and 5 years of clinical research experience (academia and/or industry). Experience in analyzing and interpreting clinical trials. Demonstrated knowledge in GCP, clinical trial design and execution, biostatistics, and regulatory requirements for clinical studies. High level of organizational and project management skills with the ability to work collaboratively in a fast-paced, team-based global matrix environment. Demonstrated success in interacting and building relationships with various internal/external stakeholders, such as Clinical Operations, Regulatory, Biostatistics, and clinical investigators.

Experience in neurology and/or rare diseases. Experience with biomarkers, wearables and digital health technologies. Experience evaluating novel therapeutic mechanisms or emerging scientific platforms. Strong written and verbal communication skills. Ability to travel to scientific meetings and clinical sites occasionally as needed (domestic and international). #LI-TD1   Job Level: Management Additional Information The base compensation range for this role is: $194,000.00-$267,000.00 Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity. Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.  In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being ; including, but not limited to: Medical, Dental, Vision, & Life insurances Fitness & Wellness programs including a fitness reimbursement  Short- and Long-Term