Precision Medicine Associate I - Temporary Position

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases.

Summary:

Works closely with Sr. Precision Medicine Associate and Manager, Precision Medicine Operations and other key personnel to implement and operationalize Precision Medicine goals within Regeneron's clinical trials. Manages tasks for central laboratory and specialty vendors on low to moderately complex clinical trials, including collecting and tracking timelines for project planning. Performs other duties as necessary to ensure optimal clinical trial execution, including assisting in executing biomarker plans.
Performs routine operational tasks which includes ability to manage, organize, file and interpret clinical trial documents and vendor specifications more independently, and present findings to their supervisor. Organize, collect and collate training materials (Lab Manual, Sample Collection Procedures, presentation slides, etc.). Must have the ability to perform operational tasks, troubleshoots problems.

Job Duties:

Study Team Support
• Liase with cross-functional study teams and sub-teams.
• Manage documents and timelines used in acquisition of clinical trial samples designated for biomarkers, precision medicine and/or exploratory research under supervision of more senior personnel.
• Supports Precision Med Ops as required for all technical and operational sample-related matters for assigned projects by liaising with internal stakeholders.
Operational Support of Biomarker and Exploratory Analysis
• Assists Precision Medicine Operations and Scientists by assessing and forecasting biomarker timelines in Microsoft Project for all clinical trials at REGN.
• Provides input on biomarker sections in clinical trial-related (such as protocols and consents) and other supporting documents under supervision of colleagues in Precision Medicine Operations.
Central Laboratory and Specialty Vendors Management
• Takes responsibility for coordination of events, liaisons with vendors, and communication with academic collaborators, when required.
• Collate and organize documents managed by Precision Medicine, including but not limited to Manuals, Validation Reports, Data files.
Data Maintenance and Management
• Supports information exchange and maintain data integrity when handing data files and information.
Compliance Maintenance in Collection and Processing of Human Biospecimen
• Provides guidance and research information regarding collection and storage of biospecimen acquired in the course of clinical trials under supervision of more senior personnel.
• Works with Precision Medicine Operations to review ICF permissions when required

Requirements:
• Working knowledge of the clinical drug development process
• Ability to use Microsoft Project for timeline planning
• Ability to update databases in a streamlined manner
• Effective problem solving skills
• Excellent written and verbal communication and presentation skills in small and large group settings
• Science background and working knowledge of a wide array of biological assays including proteomics, cellular assays, genomics, etc.
• Understanding of bioethics of human biospecimen collection and research
• Ability to effectively multi-task and prioritize
• Ability to work in a matrix environment
• Project management/organizational skills
• Interpersonal skills
• Cross-functional and cross-cultural awareness
• Excellent computer skills including Microsoft suite and Microsoft Access
EDUCATION
• B.S degree - Major/ Minor (Biology, Biochemistry or equivalent)
EXPERIENCE
• 2 + years pharmaceutical industry experience.

This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business.

To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid.

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.