Manager Global Partnerships & Trial Optimization

Regeneron Pharmaceuticals

3d • $114,800 - $187,400 • Remote

About The Position

Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, to join our Global Partnerships & Trial Optimization team. You will lead study level activities, informing our clinical development strategy, clinical study concepts, study protocols and operational plans. We play a key role in developing and maintaining relationships with external experts facilitating a wide source of country and disease area intelligence used in study design and operational planning. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

Requirements

• BS/BA required, Masters Preferred with 7+ years in Life Sciences industry or pharma consulting with a strong understanding and experience in operationalizing clinical development programs in a global setting from first-in-human to post-approval including feasibility.
• Must be a 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.
• Prior experience specifically managing feasibility strategy and execution of Hematology and/or oncology trials.

Responsibilities

• Partnering with teams during CRO led feasibility activities supporting validation of study and country level enrollment rates and study start up timelines to inform budget and baseline setting.
• Partnering with Data and Analytics function to review and identify central data sources and work with study teams to define assumptions for data curation and insight development.
• Articulating our data story based on country level feasibility and centrally derived data to support data driven decisions to enhance protocol design.
• Project management of study level country landscape assessment activities and the collection of targeted feasibility information supporting early assessment of operational feasibility for clinical trials.
• Provide functional input into the identification, qualification and relationship management of a range of vendors used in our processes.
• Develop and maintain knowledge of external clinical trial environment and assess developments for impact on study design and execution.
• Support Senior Managers in the development of study feasibility deliverables and Priority Investigator list.

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