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.
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, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible 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 parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
Salary Range (annually)
$94,800.00 - $154,600.00
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At Regeneron we believe that when the right idea finds the right team, powerful change is possible. As we work across our expanding global network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. And new ways to think about health. Connect with us so we can learn more about you, and you can learn more about our biopharmaceutical medicines. And join us, as we build a future we believe in.
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