CW Project Coordinator Data Science

Who We Are

Bio Marin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health. Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities. Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need.

We enlist the best of the best — people with the right technical expertise and a relentless drive to solve real problems — and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we’ve produced a diverse pipeline of commercial, clinical and preclinical candidates that have well‑understood biology and provide an opportunity to be first‑to‑market or offer a substantial benefit over existing therapeutic options.

From research and discovery to post‑market clinical development, our WWRD engine 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 genetic diseases.

This is a CONTRACT ROLE FOR MIN 4 MONTHS. Bio Marin Data Science is responsible for designing, capturing, analyzing, and presenting data that can drive key decisions for Clinical Development, Medical Affairs, and other business areas of Bio Marin. With a quality‑by‑design culture, Data Science builds quality data that is fit‑for‑purpose to support statistically sound investigation of critical scientific questions.

• Clinical documentation review: Conduct thorough reviews of clinical trial documentation, including protocols, consent forms, case report forms, and study reports, to ensure accuracy, completeness, and consistency with regulatory guidelines and internal standards.
• Data quality assurance: Collaborate with DMS Program Leads, DMS Study Leads and other team members to identify and resolve data discrepancies and ensure the overall quality and integrity of the clinical data.
• Regulatory compliance: Knowledge of relevant regulatory requirements (e.g. GCP, FDA guidelines) and ensure all documentation adheres to these standards.
• Documentation management: Organize, maintain, and archive electronic and physical documentation in compliance with company procedures and regulatory requirements.
• Expense Reports & Travel Planning/Scheduling: Organize, complete, follow up on expense reports and Executive travel planning and scheduling.
• Study Timelines: Generation and maintenance of GDS Study timelines with GDS and cross‑functional teams in MS Project Plan.

• High school diploma required.
• Preferred BA/BS degree with a focus in data science, statistics, computer science, life science, or related scientific discipline.
• MS Project, MS Office Suite (Word, PowerPoint, Excel) experience preferred.
• Concise, strong communication, verbal and written skills.
• Excellent organizational skills.

We will also consider applicants who act as Executive Travel Coordinator, Process Improvement Initiative contributor, and provide administrative support within the Global Data Science and Data Management Science groups.

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.