Early Development Global Study Leader

Job Title: Early Development Global Study Leader

Location: Cambridge, MA   Morristown, NJ

About the Job

Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate Progress. 

The Global Study Leaders plan, execute, and finalize clinical trial operations around the world, partnering with cross-functional study teams and overseeing the entire clinical trial process, including preparing protocols, recruiting subjects, collecting valuable data, managing budgets and timelines, etc. As a Global Study Leader, you will develop the operational study plan for multiple clinical trial sites, contributing to Sanofi's development of new drugs and medical devices through clinical trials.

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

Main Responsibilities:

• oversee the efforts in setting, conducting and closing clinical studies, ensuring smooth and efficient execution.

• defining and monitoring budgets and schedules,

• establishing study guidelines,

• delegating tasks,

• developing strategies to optimize operations, including recruitment

• evaluate and implement where applicable accelerations in study timelines

• monitor the progress of the studies, identifying risks and issues, develop mitigation plans, conducting corrective measures when needed.

• lead and coordinate the study team  to reach goals, all while implementing the company's policies and regulations, including the study's vision and mission, securing relationships with clinical sites and vendors

• coordinating local/countries operations

• selecting, coordinating and overseeing central vendors

• manage outsourced activities or CRO if applicable

• mentor GSLs, apprentices or trainees

• lead/participate in transversal activities related to clinical study processes

About You

• Earned Bachelor's degree in a scientific or life sciences field
• 2+ years of experience in clinical research preferably in clinical trial management or clinical development
• Clinical Trials Management or Project Management experience required
• Experience working with international sites/partners or working on global projects is highly preferred
• Field monitoring experience is an added value.
• Experience working with vendors and external partners is ideal
• Experience with risk management as it relates to understanding, writing and updating risk mitigation plans is very helpful
• Ability to keep updated, detailed records and communicate with multiple internal and external stakeholders regarding project progress is essential
• Ability to predict and mitigate issues before they arise, as well as the ability to troubleshoot and correct issues when they occur is key
• Ability to work on multiple projects at once, as well as to adjust to changing priorities is crucial
• Desire to work within a collaborative and cross-functional team is required

Why Choose Us?

• Bring the miracles of science to life alongside a supportive, future-focused team.

• Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.

• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.

• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

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All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.