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.

• 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.
• Exposure to cutting-edge technologies, data platforms, and feasibility methodologies.
• Professional growth and development opportunities within a globally recognized clinical research environment.
• Inclusive workplace culture that values diversity, empathy, and continuous learning.
• Access to comprehensive employee benefits and wellness programs, in accordance with company policies and local regulations.
• Opportunity to work alongside industry-leading experts in clinical development and life sciences.