Start Date
Immediate
Expiry Date
12 Oct, 25
Salary
259200.0
Posted On
13 Jul, 25
Experience
2 year(s) or above
Remote Job
Yes
Telecommute
Yes
Sponsor Visa
No
Skills
It, Visualization, Consideration, Vaccinations, Color, Data Presentation, Eligibility, Communication Skills, Professional Development
Industry
Pharmaceuticals
JOB DESCRIPTION
Job Title:
Associate Medical Director, Safety Science
Department:
Patient Safety
Reports to:
Applicable Safety Science Manager/Leader
Location:
United States (San Rafael, CA); Open to hybrid
EDUCATION AND EXPERIENCE
TECHNICAL KNOWLEDGE
Developing Skills
Professional Attributes
Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.
PLEASE NOTE: Absent a Medical or Religious reason that prohibits vaccinations, all our incoming employees must be vaccinated for COVID-19.
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, sexual orientation, national origin, disability status, protected veteran status, or any other characteristic protected by law.
The salary range for this position is: $172,800 to $259,200. BioMarin considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans.
For additional benefits information, visit: https://careers.biomarin.com/benefits.
ROLE SUMMARY
The Associate Medical Director of Safety Science provides medical expertise to support safety surveillance activities for assigned products. You will contribute to pharmacovigilance (PV) operations, perform medical safety assessments, assist with regulatory activities, and support the implementation of safety monitoring practices. This role offers the opportunity to develop clinical and regulatory expertise while ensuring patient safety and supporting product development goals.
KEY RESPONSIBILITIES
Medical Safety Support