Regeneron
PreclinicalOperationsAssociateII
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Preclinical Operations Associate II at Regeneron. Skills: Program management, Cross-functional planning, Process improvement. Deliver program management support. Facilitate development of nonclinical plans”
Industry & Context.
Identify risks; Identify issues; Identify dependencies; Identify variances; Propose solutions
What They're Looking For.
Must Have
Bachelor's or Master's degree, 2 years project or program management experience, communication skills, collaboration skills, stakeholder engagement skills, Demonstrated ability to learn quickly, adapt to new processes, adapt to new tools, adapt to new systems
What You'll Do.
Deliver program management support
Facilitate development of nonclinical plans
Facilitate alignment of nonclinical plans
Facilitate execution of nonclinical plans
Integrate nonclinical activities into project plan
Monitor progress against approved plans
Identify dependencies
Communicate dependencies
Communicate variances
Coordinate Sub-Team(s)
Build working relationships
Maintain working relationships
Maintain nonclinical program information
Contribute to process improvement initiatives
Identify opportunities for improvement
Propose solutions for improvement
Support implementation of improvement
Provide operational support
Provide systems support
Offer constructive feedback
Collaborate with team members
Collaborate with functional colleagues
Address project challenges
Address team challenges
How You'll Work.
Team & Collaboration
Functional stakeholders; Cross-functional stakeholders
Communication Scope
Communication; Stakeholder engagement
Process & Methodology
Program management, Cross-functional planning, Timeline management, Risk identification, Issue identification, Dependency management, Variance analysis
Full Job Description
The Preclinical Operations Associate II provides cross-functional program management support across **Preclinical Operations (PCO)** , **Bioanalytical Sciences (BAS)** , **Scientific Writing (SW)** , and **Drug Safety and Pharmacometrics (DSP)**. This role enables effective planning, alignment, execution, and communication of PCO, BAS, SW and DSP activities in support of development programs. **Responsibilities during a typical day might include the following:** * Independently deliver comprehensive program management support to PCO, BAS, SW, and DSP functions. * Facilitate the development, alignment, and execution of nonclinical cross-functional plans, timelines, and deliverables for assigned program(s). * Integrate nonclinical activities into the broader project plan to ensure alignment with overall development objectives. * Proactively monitor progress against approved plans, identifying and communicating risks, issues, dependencies, and variances. * Lead and coordinate appropriate Sub-Team(s) for assigned program(s), ensuring clear objectives, accountability, and effective decision-making. * Build and maintain strong working relationships with functional and cross-functional stakeholders to influence outcomes and gain alignment. * Maintain accurate, current nonclinical program information in corporate planning and collaboration tools (e.g., Planisware, SharePoint, Teams, MS Project). * Contribute to process improvement initiatives by identifying opportunities, proposing solutions, and supporting implementation. * Provide limited operational or systems support, as needed, to enhance communication, collaboration and efficiency across supported functions. * Offer constructive feedback and collaborate with team members and functional colleagues to address project and team challenges. **This role may be for you, if you:** * Bachelor’s or Master’s degree in a relevant scientific or technical field. * Minimum of 2 years of project or program management experience. * St
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