Strategic Feasibility Senior Manager - Europe/US - Remote in Nottingham

Who We Are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way. Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands‑on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritise cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!

What The Feasibility Department Does At Worldwide

Here at Worldwide, we are scientifically driven and committed to making a difference in patient lives, and Feasibility is where it all begins! We are on the front lines in study planning and execution, building the foundation for study success. Members of our strategic feasibility team contribute to advancing the field of feasibility through creative problem‑solving using advanced analytics and visualisations. We collaborate with senior leaders in our organization and potential clients across the globe to build viable protocols, appropriately position studies geographically, and allocate optimal timelines. Our Strategic Feasibility team is the perfect next step for your career!

What You Will Do

• The Strategic Feasibility Senior Manager will develop strategies for successful trial conduct through the acquisition, analysis, and application of data. This will be demonstrated primarily in proposals, bid defenses, and stand‑alone feasibility projects.
• This person will support the vision and leadership of the Feasibility team.
• Lead the feasibility process for proposals and bid defenses including the development of clear and compelling content, utilising various data sources to deliver customised recommendations regarding site and country mixes, timelines, and other factors related to the conduct of a trial.
• Ensure customer service (internal & external customers), timelines & quality expectations are met and/or exceeded.
• Develop and maintain collaborative relationships with Worldwide Therapeutic Area Leads, Medical & Scientific Affairs leads, Medical Directors, Regulatory Experts, and other stakeholders to support the feasibility process.
• Educate internal and external customers regarding the principles of data‑driven feasibility.
• Assist in the identification of new data sources, the development of new analytical approaches, and/or the development of new tools to support the feasibility process.

What You Will Bring To The Role

• An effective communicator, both written and spoken English, who demonstrates the ability to write persuasively and develop compelling visualisations (charts, graphics, etc.).
• Ability to think creatively and solve problems.
• Ability to process information quickly and dynamically adapt to new information.
• An accomplished negotiator with the ability to influence and present to small and large groups.
• Ability to work at a fast pace with short timelines and minimal oversight.
• Ability to work collaboratively with other functions as needed in the pre and post‑award setting.
• Ability to travel approximately 20% for business needs (domestically and internationally).
• Excellent organisational skills.

Your Experience

• 7+ years’ of transferrable experience in industry, health care, or data driven feasibility, at least 2 of which CRO, preferably feasibility.
• Background in medicine, science, or other relevant discipline with a substantial international experience in clinical drug development across a broad range of therapeutic areas.
• Knowledge of the principles of Good Clinical Practice.
• Minimum Bachelor’s degree.
• Must have competent computer skills in MS Word, Excel, and PowerPoint.

We love knowing that someone is going to have a better life because of the work we do.