Associate Medical Director, Clinical Development Rare Movement Disorders
About The Position
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.
Requirements
- 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.
Nice To Haves
- 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).
Responsibilities
- 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.
Benefits
- Medical, Dental, Vision, & Life insurances
- Fitness & Wellness programs including a fitness reimbursement
- Short- and Long-Term Disability insurance
- A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
- Up to 12 company paid holidays + 3 paid days off for Personal Significance
- 80 hours of sick time per calendar year
- Paid Maternity and Parental Leave benefit
- 401(k) program participation with company matched contributions
- Employee stock purchase plan
- Tuition reimbursement of up to $10,000 per calendar year
- Employee Resource Groups participation
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What This Job Offers
Job Type
Full-time
Career Level
Manager
