Associate Director - Global Trial Optimization

Temp Associate Director - Global Trial Optimization

Pay Range: $58.80 - $171.01/hr

Remote Role (US Only)

12 Month Contract

The Temp Associate Director, Global Trial Optimization (GTO) is responsible for providing strategic insights, expert recommendations, tailored training content, and specialized deliverables in support of the GTO leadership team’s core process areas (strategic feasibility, site identification, patient engagement, and enrollment planning).

We expect the Associate Director to demonstrate their advanced feasibility knowledge and extensive experience, and involve collaborating with leaders and internal collaborators to drive new GTO process development and optimize current strategies. We believe the A/D will lead and provide expert guidance to ensure operational excellence and consistent, effective, high-quality project delivery through development of the onboarding process of new team members and the ongoing training and support of current team members. The role reports into the Head of Global Trial Optimization.

In this role, a typical day might include:

• Provides leadership input and expertise in support of GTO team’s generation of consistent, high-quality, and timely insights to inform study design, study placement, operational planning, and patient and site engagement strategies
• Partners with GTO Head and capability process leads, providing expert insights and recommendations into the development of GTO strategy & process, ensuring that expectations for key GTO deliverables are met.
• Contributes as a Subject Matter Expert to the development and implementation of core GTO functions, processes, and procedures, as well as cross-functional and organizational process improvement initiatives as required.
• Uses company and department-level experience and strategic analysis to develop and drive viable, enduring solutions to optimize strategic feasibility and patient engagement delivery

This role might be for you if have:

• Extensive experience in global clinical trial operations required
• Compelling communicator with ability to deliver accessible scientific and technical information to a variety of audiences
• Proven ability to lead teams and build strong internal and external working relationships in a diverse range of environments
• Experience in leading activities and providing strategic input that aligns with clinical development plans (CDPs)

To be considered for this opportunity, we expect you to have at least 8 years of trial optimization experience within a sponsor or CRO environment. We also require the AD to have a bachelor's degree at a minimum.

This is a contract position at Regeneron with Magnit Global being the Employer.

To do our best work we need different viewpoints. Therefore, we celebrate diversity and embrace inclusion. As an equal opportunity employer, we are dedicated to building a team that represents a variety of backgrounds, perspectives, and skills. We strive to ensure that we maintain a positive and enriching work environment for all.

W2 only, no third party solicitation