Preclinical Operations (PCO) is seeking a dynamic Associate Manager, Preclinical Operations to join the team. Using program management knowledge and experience in the drug development industry, the successful candidate would provide operational and Project Management support to Preclinical Development (PCD) and Drug Safety & Pharmacometrics (DSP) for multiple assigned projects. The successful candidate would also provide guidance and input to cross-functional project teams to enable projects to drive to completion.
This role has a 3-day onsite minimum requirement in Tarrytown, NY. Relocation can be provided.
A typical day as an Associate Manager looks like:
- Facilitates development and alignment of integrated PCD/DSP cross-functional project deliverables, plans, timelines and resources, to align with the overall project plan throughout the project lifecycle from preclinical through commercialization.
- Ensures effective execution of project plan to enable completion of PCD/DSP activities within agreed timeline, quality, and budgetary constraints.
- Effectively communicates progress and variance against the approved plan. Proactively identifies and drives resolution of critical issues, risks, and obstacles that may impact the assigned program(s).
- Enables and builds effective relationships to influence and gain cooperation of others.
- May provide operational Project Management support to PCD function(s), initiatives, collaborations etc. as needed.
- Applies technical knowledge (e.g., functional, scientific, drug development, project management etc.) and frequently contributes to development and implementation of new and unique concepts, techniques, and standards.
- Contributes to, supports, and champions standardization of processes, metrics, and communication to build efficiencies within PCD and DSP. Independently identifies areas for process improvement and proposes quality solutions.
- Effectively collaborates across project teams, functions, and departments.
This role may be for you if:
- You enjoy working in a highly collaborative setting.
- You have excellent collaborative and communication skills.
- You have demonstrated ability to multi-task, in order to meet multiple deliverables.
- You have experience in a variety of therapeutic modalities and approaches.
In order to be considered, this role requires a BS/MS degree with a minimum of 7+ years of relevant R&D operational and/or project management experience in the drug development/pharmaceutical industry. Ability to lead, coordinate, and facilitate development, alignment, and execution of project plans and budget forecasts. A background knowledge in Toxicology/Drug Safety is preferred.
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits.
Salary Range (annually): $94,800.00 - $154,600.00
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