CW Project Coordinator Data Science; TEMPORARY

Overview

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 to understand the underlying causes of genetic conditions and create transformative medicines that address significant unmet medical needs. With a distinctive focus on genetics and molecular biology, our pipeline spans the development of first‑in‑class and best‑in‑class therapeutics designed to offer substantial clinical benefits.

Worldwide Research and Development (WWRD):
From discovery to post‑market clinical development, our WWRD engine involves all bench and clinical research. The teams work on developing first‑in‑class and best‑in‑class therapeutics that provide meaningful advances to patients living with genetic diseases.

This is a contract role for a minimum of four months. The Bio Marin Data Science team designs, captures, analyzes, and presents data that drives key decisions for Clinical Development, Medical Affairs, and other business areas. The Data Management Science (DMS) group ensures complete, correct, and consistent analyzable data and oversees data management activities such as protocol review, eCRF development, data validation, and reconciliations.

The Project Coordinator ensures the accuracy, completeness, and integrity of clinical trial data and documentation, manages study timelines, organizes meetings and administrative support, and also serves as Executive Travel Coordinator and Process Improvement contributor as needed.

• Design, capture, analyze, and present data for Clinical Development, Medical Affairs, and other business areas.
• Build quality data that is fit‑for‑purpose to support statistically sound investigations of scientific questions.
• Ensure complete, correct, and consistent data at the data structure and documentation levels in accordance with international standards and GCP.
• Oversee data management activities: protocol review, eCRF development, data validation, reconciliations, and data quality validation.
• Conduct thorough reviews of clinical trial documentation (protocols, consent forms, case report forms, study reports) to ensure accuracy and consistency.
• Collaborate with DMS Program Leads and Study Leads to identify and resolve data discrepancies and maintain overall data quality and integrity.
• Ensure regulatory compliance with GCP, FDA guidelines, and other applicable regulatory requirements.
• Organize, maintain, and archive electronic and physical documentation in compliance with company procedures and regulatory requirements.
• Generate and maintain GDS study timelines in MS Project with cross‑functional teams.
• Manage expense reports and execute Executive travel planning and scheduling.
• Provide administrative support and coordinate meetings, agendas, and minutes.

• High school diploma required; preferred BA/BS in data science, statistics, computer science, life science, or related discipline.
• MS Project, MS Office Suite (Word, PowerPoint, Excel) experience preferred.
• Strong communication skills (verbal and written).
• Excellent organizational skills.
• Experience with regulatory requirements such as GCP and FDA guidelines.
• Ability to work independently and as part of a cross‑functional team.

Salary range: $51 to $75 per hour. The base pay will consider internal equity and may vary based on geographic region, experience, qualifications, and role. The position may also be eligible for discretionary annual bonus, stock‑based long‑term incentives, paid time off, and a benefits package that includes company‑sponsored medical, dental, vision, and life insurance.

For additional benefits information, visit:

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.