[Hiring] Strategic Feasibility Senior Manager @Worldwide Clinical Trials

Role Description

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, utilizing various data sources to deliver customized 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.

Qualifications

• An effective communicator, both written and spoken English, who demonstrates the ability to write persuasively and develop compelling visualizations (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 organizational skills.

Requirements

• 7+ years of transferrable experience in industry, health care, or data-driven feasibility, at least 2 of which in a CRO, preferably feasibility.
• Background in medicine, science, or other relevant discipline with 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.

Benefits

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