Temp - Preclinical Operations Project Associate I

The Preclinical Operations team is currently seeking a Temp - Preclinical Operations Project Associate I to join the team. In conjunction with Bioanalytical Strategy Group (BSG) and Preclinical Operations (PCO), provides operational support for nonclinical and clinical GxP bioanalytical work being conducted at Contract Research Organizations (CROs). With direct supervision, uses prior knowledge of GxP and bioanalytical sciences to provide operational support to aid coordination, monitoring and tracking of outsourced bioanalytical activities (nonclinical and clinical) in order to enable progression of internal and external programs.

As a Preclinical Operations Project Associate I, a typical day may include:

-  Contributing to scientific and technical aspects for each bioanalytical activity
-  Project initiation and kickoff
-  Project planning and tracking
-  Monitoring and tracking CRO invoicing
-  Monitoring and tracking status of bioanalytical assays, sample analysis and reporting
-  Meeting logistics (invites, agenda, meeting facilitation, meeting minutes, follow up on action items)
-  Timely identification of issues and risks associated for each bioanalytical activity and contribute to risk mitigation solutions
-  Regular communication of progress, issues and risks for each bioanalytical activity to key stakeholders
-  Support for contracting and procurement

This role may be for you if:

-  You are action oriented and organized
-  You demonstrate excellent written, verbal and interpersonal communication skills with the ability to effectively interact with team members with tact and diplomacy
-  You have Proven ability to forge strong working relationships with department/function leaders as well as subject matter experts.
-  You can handle multiple projects and priorities with excellent time management skills (both project and self)

To be considered for this role, you must have a BS/MS with 2-3 years of experience with the working knowledge of bioanalytical sciences and project management as they apply to the drug development / pharmaceutical industry. Which includes but is not limited to the following: Understanding of pre-clinical and clinical protocols/ amendments so that time points and collection details, etc. are correctly identified and utilized. We need someone who has an understanding of bioanalytical requirements such as tube types, matrix specifications, etc. We are looking for an individual who is proficient in relevant software: MS Project, MS Teams, Excel, PowerPoint, Word, etc. in addition to general knowledge of shared work environments.


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.