Precision Medicine Associate II

Tarrytown, NY, United States
Apr 09, 2021
Required Education
Position Type
Full time
As a Precision Medicine Associate II you will work to implement and operationalize Precision Medicine goals within our clinical trials, focused on immuno-oncology. You will manage central laboratory and specialty vendors on low to moderately complex clinical trials. Executes biomarker plans in collaboration with the team. Performs routine operational tasks, begins to manage, organize, and interpret clinical trial documents and vendor specifications more independently, and presents findings to his/her supervisor. Presents at investigators meetings and crafts training materials (Lab Manual, Sample Collection Procedures, presentation slides, etc.). Supports senior staff on highly complex trials.

A typical day may include:
  • Participates in cross-functional study teams and sub-teams.
  • Manages acquisition of clinical trial samples designated for biomarkers, precision medicine and/or exploratory research.
  • Supports individual clinical study teams as required for all technical and operational sample-related matters for assigned projects by liaising with internal partners.
  • Assists Precision Medicine Strategy Leads 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.
  • Prepares RFPs, reviews and assess bids and SOWs.
  • Coordinates capabilities presentations by novel vendors.
  • Attends conferences to identify new methodologies and technologies.
  • Takes responsibility for coordination of events, liaisons with vendors, and communication with academic collaborators.
  • Participates in oversight activities with vendors and supports audits as required.
  • 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.
  • Supports sample and data reconciliation activities.
  • Provides guidance to clinical study teams and clinical sites regarding collection and storage of biospecimen acquired in the course of clinical trials.
  • Works with ICF Specialist and Precision Medicine Strategy Lead to ensure compliance with ICF permissions.
This may be for you if:
  • Are interested in the management of immune-oncology clinical trials and research.
  • Can multi-task with effective project management/organization skills.
  • Thrive in a high-paced and invigorating environment.
  • Are process driven with attention to detail
  • Can work independently to achieve group initiatives and goals
To be considered you are required to have a Bachelors degree with a major or minor in Biology or equivalent. Your experience should include 2 - 6 years pharmaceutical industry experience with a science background and working knowledge of a wide array of biological assays including proteomics, cellular assays, genomics, etc. Solid understanding of bioethics of human biospecimen collection and research is necessary

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.