Preclinical Operations Associate II

Regeneron Pharmaceuticals • Tarrytown, GA

3d • $71,800 - $116,800 • Onsite

About The Position

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.

Requirements

• Bachelor’s or Master’s degree in a relevant scientific or technical field.
• Minimum of 2 years of project or program management experience.
• Strong communication, collaboration, and stakeholder engagement skills.
• Demonstrated ability to learn quickly and adapt to new processes, tools, and systems.

Responsibilities

• 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.

Benefits

• health and wellness programs (including medical, dental, vision, life, and disability insurance)
• fitness centers
• 401(k) company match
• family support benefits
• equity awards
• annual bonuses
• paid time off
• paid leaves (e.g., military and parental leave)

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level