Manager, Precision Medicine

Location
Tarrytown, NY, United States
Posted
Aug 23, 2020
Ref
20636BR
Required Education
Associate Degree
Position Type
Full time
Summary:As a Manager- Precision Medicine you will work closely with Director, Precision Medicine and other key personnel to implement and operationalize Precision Medicine goals within Regeneron's clinical trials. Manages central laboratory and specialty vendors on clinical trials. Presents at investigators meetings and builds training materials (Lab Manual, Sample Collection Procedures, presentation slides, etc.). Supports and/or manages Senior Associates and Associate Managers to execute team the organizations goals.

Job responsibilities:
Study Team Support
  • Participates in cross-functional study teams and sub-teams.
  • Manages acquisition of clinical trial samples designated for biomarkers, precision medicine and/or exploratory research under supervision of more senior personnel.
  • Supports individual clinical study teams as the need arises for all technical and operational sample-related matters for assigned projects by collaborating closely with internal partners.

Operational Support of Biomarker and Exploratory Analysis
  • Assists Precision Medicine Scientists by assessing vendors, forecasting the biomarker sample operational costs, and reviewing invoices.
  • Provides input on biomarker sections in clinical trial-related (such as protocols and consents) and other supporting documents.
  • Selection of Central Laboratory and Specialty Vendors
  • Prepares RFPs, reviews and assess bids and SOWs.
  • Coordinates capabilities presentations by novel vendors.
  • Attends conferences to identify new methodologies and technologies.

Central Laboratory and Specialty Vendors Management
  • Takes ownership for coordination of events, liaisons with vendors, and communication with academic collaborators.
  • Participates in oversight activities with vendors and supports audits as required.

Data Maintenance and Management
  • Supports information exchange and maintain data integrity.
  • Provides guidance and training to clinical sites, collaborators and vendors to enable transfer of biomarker and exploratory data under supervision of more senior personnel.
  • Supports sample and data reconciliation activities.
Compliance Maintenance in Collection and Processing of Human Biospecimen
  • Provides guidance to clinical study teams and clinical sites regarding collection and storage of biospecimen acquired in the course of clinical trials under supervision of more senior personnel.
  • Works with ICF Specialist and Precision Medicine Scientist to ensure compliance with ICF permissions.

This may be for you if:
  • You thrive in a cross functional matrix organization.
  • You like to work with a wide array of biological assays including proteomics, cellular assays, genomics, etc.
  • You want to see your impact on teams goals.
  • You have the desire to see projects and process from inception through completion.
Job requirements
To be considered for this, you should have a minimum of a B.S degree with a Major or Minor in Biology, Biochemistry or equivalent with 8+ years of pharmaceutical industry experience and a solid understanding of the clinical drug development process. Your experience should include an understanding of bioethics of human biospecimen collection and research. Strong Project management/organizational skills are required

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.