Regeneron · 22 hours ago
Senior Manager Global Partnerships & Trial Optimization
United States
Full-time
Remote
Senior Level, Lead/Staff
$134K/yr - $219K/yr
8+ years expRegeneron is a leading biotechnology company, and they are seeking a Senior Manager for Global Trial Optimization. This role involves leading study level activities to advise on clinical development strategies and maintaining relationships with external experts to inform study design and operational planning.
BiopharmaBiotechnologyPharmaceutical
Responsibilities
Lead study level feasibility processes to generate high quality and timely data to inform study design, efficient geographical placement and operational planning
Partner with teams during CRO led feasibility activities supporting validation of study and country level enrollment rates and study start up timelines to advise budget and baseline setting
Supports the development and implementation of the Global Trial Optimization function through process initiatives and change management
Partner with Data and Analytics function to review and identify appropriate central data sources
Articulate the data story to teams based on country level feasibility and centrally derived data to support data driven decisions to improve protocol design
Project management of study level country landscape assessment activities and the collection of targeted feasibility information for early assessment of operational feasibility for conducting clinical trials
Lead study level engagements to acquire, analyze and deliver high quality targeted information from external partners
Prove input into continuous improvement activities to ensure consistency of process execution
In partnership with Clinical Outsourcing provide functional input into the identification, qualification and relationship management of a range of vendors
Develop and implement patient recruitment and retention tactics aligned with defined study strategy
Develop and maintain knowledge of external clinical trial environment and assess developments for impact on study design and execution
May require up to 20% travel
Qualification
Required
Bachelors degree in a related field
Minimum of 8 years of relevant industry experience within pharma/biotech, a CRO or consulting
Strong understanding and experience in operationalizing clinical development programs in a global setting from first-in-human to post-approval
Compelling communicator with ability to translate sophisticated messages to a variety of audiences
Experience in using data to inform clinical strategy development
Ability to understand sophisticated business questions and develop effective solutions
Experience in process development, implementation and change management activities
Preferred
Line management experience
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)
Company
Regeneron
Regeneron Pharmaceuticals specializes in the discovery, development, and commercialization of innovative medicines.
10001+ employees
H1B Sponsorship
Regeneron has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (157)
2024 (128)
2023 (128)
2022 (137)
2021 (104)
2020 (122)
Funding
Current Stage
Public CompanyTotal Funding
$15.93MKey Investors
U.S. Department of Health & Human Services
2024-07-11Post Ipo Equity· $2.03M
2023-10-18Post Ipo Equity· $5M
2016-08-22Post Ipo Equity· $8.9M
Leadership Team
Aris Baras
Senior Vice President, Regeneron Pharmaceuticals, General Manager, Regeneron Genetics Center
Bari Kowal
Senior Vice President, Head Development Operations & Portfolio Management
Recent News
2026-02-02
2026-02-02
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