Site Feasibility Manager

About This Role The Site Feasibility Manager will lead and execute in‑house end‑to‑end site feasibility activities, oversee and manage cross‑functional stakeholders to meet key timelines, and develop high‑quality outreach reports to present to SMTs. This role also conducts data‑driven research to support clinical trial feasibility for Biogen’s clinical development programs. The ideal candidate will be skilled in managing and collaborating effectively across functions, assessing study‑specific data analysis needs, and partnering with Program Feasibility Leads to develop innovative data visualization deliverables that enhance decision‑making. Depending on business needs and departmental goals, the position may be required to focus on interconnected areas within Biogen Quantitative Sciences and Development Operations, leveraging similar skills and knowledge base, including study start‑up technologies, analytics, and project management of process improvement initiatives. The Site Feasibility Manager reports into the Director of the Feasibility Center of Excellence. What You’ll Do Lead and execute end‑to‑end in‑house site feasibility activities whilst managing cross‑functional stakeholders across clinical programs. Manage creation, sending, tracking and results reporting of the site feasibility questionnaire process for outreach to sites using Veeva Clinical. Conduct data analysis to generate comprehensive site feasibility reports and site ranking to present to key stakeholders. Conduct analytical data‑driven feasibility research using clinical trial datasets, real‑world data, and internal resources to inform program and study‑level strategy. Assess clinical trial study designs and develop visualizations and data outputs to support evaluation of protocol complexity and patient and site burden. Maintain detailed records of work and internal databases. Engage with Program Feasibility Leads to support scenario modelling for impact to clinical trial operational designs. Who You Are The ideal candidate enjoys being part of the process of finding the right sites and investigators for clinical trials. You excel at data analysis and visualization and enjoy working with stakeholders across a broad organization to drive key business decisions. You have strong organizational skills, including the ability to prioritize needs and handle a high volume of tasks within a given timeframe. Required Skills Bachelor’s degree required; Master’s or PhD in an associated drug development field preferred. 4+ years of biotech, pharmaceutical or CRO clinical operations experience and/or early engagement/site feasibility management. Excellent decision‑making, communication, and presentation skills. Preferred Skills Previous experience conducting site feasibility activities in Veeva Clinical or a similar platform. Demonstrated success in working cross‑functionally in a global matrix organization. High proficiency in analysis and data visualization tools; essential experience with Excel, VBA/macros preferred. Additional experience with visualization tools such as Power BI, Spotfire, Tableau, statistical analysis/programming. Additional Information Base compensation range: $122,000.00 – $163,000.00. Salary is determined through an analytical approach utilizing relevant skills, experience, location, and internal equity. Benefits Short‑term and long‑term incentives, including cash bonus and equity opportunities. Medical, Dental, Vision, and Life insurances. Fitness & Wellness programs with reimbursement. Short‑ and Long‑Term Disability insurance. 15 days of paid vacation plus end‑of‑year shutdown time off (Dec26‑Dec31). 12 company‑paid holidays + 3 paid personal significance days. 80 hours of sick time per calendar year. Paid Maternity and Parental Leave benefits. 401(k) with company matching. Employee stock purchase plan. Tuition reimbursement up to $10,000 per calendar year. Employee Resource Groups participation. EEO Statement All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E‑Verify Employer in the United States. #J-18808-Ljbffr Biogen, Inc.