Senior Clinical Science Specialist II (Associate Director Equivalent) / Senior Clinical Scientist (Sr. Manager Equivalent) - United States
Want to know company name or location? Company managed [?]
BioMarin is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases. We target diseases that lack effective therapies and affect relatively small numbers of patients, many of whom are children. These conditions are often inherited, difficult to diagnose, progressively debilitating and have few, if any, treatment options. BioMarin will continue to focus on advancing therapies that are the first or best of their kind.
BioMarin’s Development Sciences group is responsible for everything from research and discovery to post-market clinical development. Development Sciences involves all bench and clinical research and the associated groups that support those endeavors. Our teams work on developing first-in-class and best-in-class therapeutics that provide meaningful advances to patients who live with rare diseases. Come join our team and make a meaningful impact on patients’ lives.
Clinical Sciences is seeking a passionate and driven clinical science specialist with an interest in translational medicine to help support mid- and late-stage clinical programs as well as to provide clinical input on early-stage programs across the portfolio.
Provide Clinical Science support to mid- and late-stage clinical program(s), including
Work with study team to design and execute clinical studies aligned with company objectives
Assist medical monitor(s) with review of emerging safety and efficacy data
Assist medical writers with generation of Protocols, CSRs, communications to regulatory authorities and other relevant program and study documents
Work with team to provide Clinical Sciences data- and evidence-based input and guidance on programs potentially entering the company pipeline:
Includes both internal research programs and programs being reviewed for potential in-licensing
Assess feasibility of clinical path and fit with company strategy
- Minimum of 4 years working in clinical development with hands-on study and program experience
- Experience in early-stage/translational development (minimum 3 years)
- Experience in due-diligence or similar business development activities
- Experience across a variety of therapeutic areas
Ph.D or Pharm.D. or M.D.
Cross-functional clinical study team – clinical operations, biometrics, program management, medical writing, clinical pharmacology, toxicology, research, commercial, regulatory affairs
Portfolio prioritization – research, business development, commercial
None at the outset
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.