Senior Manager, Feasibility

**This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Manager, Feasibility based in the United States.** Join an impactful opportunity at the forefront of clinical development, where scientific insight and data-driven decision-making help shape the success of global clinical trials. This role is ideal for an experienced feasibility professional who thrives in collaborative, cross-functional environments and enjoys influencing early-stage study strategy. You will play a critical role in evaluating study viability, identifying optimal countries and sites, and leveraging advanced data sources to support patient recruitment success. Working closely with clinical, real-world evidence, and operational teams, you will contribute to the development of innovative feasibility capabilities while helping accelerate access to life-changing therapies worldwide. This position offers a unique blend of strategic thinking, scientific evaluation, and operational leadership within a highly mission-driven environment. ### Accountabilities: - Lead early-stage feasibility and viability assessments for proposed clinical studies, providing scientific and operational recommendations regarding study execution. - Evaluate study concepts and protocol requirements to determine optimal country, site, and investigator selection strategies. - Utilize feasibility technologies and data platforms, including real-world evidence tools, to generate insights on patient populations, enrollment potential, and study risks. - Prepare comprehensive feasibility reports detailing enrollment projections, therapeutic landscapes, local treatment practices, protocol considerations, and site identification strategies. - Collaborate cross-functionally with clinical operations, monitoring teams, real-world evidence experts, and other stakeholders to support informed decision-making. - Contribute to the implementation of new technologies, processes, and methodologies that enhance feasibility capabilities and operational efficiency. - Review and validate feasibility deliverables to ensure quality standards and timeline commitments are consistently achieved. - Support team growth initiatives, including capability building, process improvement, and potential involvement in recruitment activities. - Maintain compliance with applicable regulations, industry standards, and internal procedures, including ICH-GCP requirements. ## Requirements - Bachelor's degree in Life Sciences, Health Sciences, or a related field required; Master's degree or Health Data Sciences qualification preferred. - Minimum of 5 years of relevant experience within clinical research, pharmaceutical, biotechnology, or related industries. - Strong scientific understanding of therapeutic areas and clinical trial methodologies. - Demonstrated experience conducting clinical trial feasibility, study viability assessments, or site and country selection activities. - Excellent knowledge of Good Clinical Practice (GCP), regulatory requirements, and global clinical development processes. - Experience utilizing feasibility platforms, data analytics tools, and real-world evidence solutions to support decision-making. - Proven ability to author scientific reports and communicate complex findings in a clear and actionable manner. - Prior experience managing teams or leading cross-functional initiatives is highly desirable. - Strong analytical, organizational, and stakeholder management skills, with the ability to influence decisions in matrixed environments. - Excellent written and verbal communication skills, combined with a proactive and collaborative mindset. ## Benefits - Fully remote working opportunity within the United States. - Opportunity to contribute to global clinical research programs that directly impact patient outcomes. - Collaborative and mission-driven work environment focused on innovation and scientific excellence. - Exposur…