Associate Director, Regulatory Affairs jobs in United States
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Biogen · 1 day ago

Associate Director, Regulatory Affairs

Biogen is a mid-sized biotechnology company committed to excellence and innovation. They are seeking an Associate Director in Regulatory Affairs to develop and execute global regulatory strategies for product development and approval, while leading interactions with major Health Authorities and providing regulatory support across various departments.

BiotechnologyHealth CareNeuroscienceTherapeutics
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Comp. & Benefits
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H1B Sponsor Likelynote

Responsibilities

Responsible for developing and executing global regulatory strategies for assigned projects and programs
Support development of the preclinical and clinical development plan
Identify and assess regulatory risks associated with product development. Define mitigation or contingency strategies
Set strategic direction and leads global regulatory submission process with submission teams, including IND, CTA and core briefing packages
Prepare and/or lead global regulatory submissions including IND, pre-IND meeting package, CTA
Mentor Regulatory Managers
Build and maintain excellent relationships with relevant regulatory agencies, contractors and corporate partners while negotiating company position
Provide leadership on project teams and subcommittees in all areas of regulatory affairs and product development
Provide input to Senior Management teams
Maintain a global view as part of the whole regulatory team

Qualification

Regulatory AffairsPharmaceutical Industry ExperienceRegulatory SubmissionsGCPsGLPs KnowledgeGene Therapy ExpertiseLeadership SkillsCommunication SkillsOrganizational SkillsInterpersonal SkillsMentoring Experience

Required

BA/BS/University degree, Life/Health Sciences preferred
8 years pharmaceutical/biotechnology industry experience with technical management experience
Minimum of 6 years in RA
Comprehensive knowledge of applicable regulations
Experience in interpretation of regulations, guidelines, policy statements, etc
Experience and knowledge in the preparation of major regulatory submissions and supportive amendments or supplements
Experience working on products in development specifically relating to clinical and pre-clinical regulatory aspects of the project
Knowledge of regulations governing the development of drugs
Solid knowledge of GCPs and GLPs
Direct experience in interfacing with relevant regulatory authorities (FDA)
Foster effective, positive interactions with regulatory agencies, and corporate partners
Ability to lead and influence project teams, committees, etc. to attain group goals
Demonstrate excellent leadership and communication skills
Ability to represent the department in project teams, committees and external meetings
Demonstrate strong organizational skills, including the ability to prioritize personal workload
Strong interpersonal skills and the ability to deal effectively with a variety of senior personnel including medical, scientific, and manufacturing staff
Strong sensitivity for a multicultural/multinational environment. Experience leading multi-disciplinary teams
Well organized, detail oriented, effective written and oral communication skills
Supervisory/mentoring experience
Ability to guide, train, supervise and prioritize workload of direct reports if applicable
Expert knowledge and experience in gene therapy highly desirable

Preferred

Graduate degree
Some international regulatory experience preferred
Experience with biologics preferred

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

Company

Biogen is an American biotechnology company that provides therapeutics for neurological, autoimmune, and rare diseases.

H1B Sponsorship

Biogen has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (100)
2024 (93)
2023 (101)
2022 (134)
2021 (104)
2020 (114)

Funding

Current Stage
Public Company
Total Funding
$1.5B
Key Investors
JP Morgan
2023-08-28Post Ipo Debt· $1.5B
1991-09-27IPO

Leadership Team

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Robin C. Kramer
Executive Vice President, Chief Financial Officer
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Priya Singhal
Executive Vice President, Head of Development
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Company data provided by crunchbase