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Regeneron Pharmaceuticals Precision Medicine Lab Coordinator in Tarrytown, New York

The Precision Medicine Laboratory Coordinator acts as the Precision Medicine point for central and specialty labs in a fast-paced clinical trial program. This role oversees all samples through the process from the time of collection to the point of analysis and destruction. This position is expected to become an expert on the external laboratory systems and processes and support the broader study team to ensure issues are monitored and resolved in a timely manner.

A typical day may include the following:

Work with Precision Medicine Scientists and study teams to coordinate biosample collection, testing and analysis with central and specialty labs

Become a guide on study protocols, schedules of events, sample collection procedures, etc.

Establish relationships, structure and oversight with lab vendors (working with Vendor & Relationship Management team as appropriate)

Contribute to collection, sample schedules, testing and analysis requirements and documentation

Support database lock planning, query resolution, sample data reconciliation

Provide clear direction to labs and support staff on procedures related to query investigation and sample reconciliation decision making

Deliver program and study level updates to Precision Medicine team and clinical development team

Oversee testing validation requirements, processes and timelines with the lab vendors

Attend relevant meetings, contribute agenda items, relevant updates, take actions and participate in resolution

Raise issues as appropriate, involve assistance with complex issues

Work with quality teams to raise, document, investigate and manage quality issues, including CAPA tracking

Work with analytics team to develop and use oversight reports to identify missing samples and/or sample data issues

Contribute to continuous improvements with the labs and internally to improve processes, efficiencies, quality and workflow

This may be for you if you:

• Ability to handle and resolve problems on the fly

• Strong project management and organizational skills

• Ability to work independently and proactively while still contributing to group initiatives and goals

• Strong interpersonal skills and ability to work with many different groups/teams to achieve success

To be considered for this you should have of 5+ years of proven experience in related role within clinical development at a Pharmaceutical, Biotechnology company, laboratory or CRO. Your experience with samples should the process from the time of collection to the point of analysis and destruction. Working knowledge of clinical trials, clinical laboratory processes & systems, clinical databases is required. Comprehensive knowledge and practice using efficiency, collaboration and operations management applications and collaboration tools (e.g. Microsoft Excel, Powerpoint, Teams, Smartsheet)

Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides amazing benefits including health and wellness programs, fitness centers and stock for employees at all levels!

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or maternity status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.

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