Site Feasibility Manager

Biogen

Site Feasibility Manager conducting in-house feasibility activities and collaborating with stakeholders for Biogen's clinical trials. Delivering data-driven insights and high-quality outreach reports.

Posted 7/3/2026full-timeCambridge • Massachusetts • 🇺🇸 United StatesMid-LevelSenior💰 $122,000 - $163,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in site feasibility management and clinical operations, utilizing data analysis and visualization tools to inform clinical trial strategies. Proficient in stakeholder engagement and cross-functional collaboration within a global matrix organization.

Highest-signal resume keywords

Site Feasibility ManagementData AnalysisVeeva ClinicalData VisualizationCross-Functional Collaboration

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical OperationsSite Feasibility ActivitiesStatistical AnalysisExcelVBAPower BISpotfireTableauData ReportingScenario Modelling

Soft Skills

Decision-MakingCommunicationPresentation Skills

Certifications & Qualifications

Bachelor’s DegreeMaster’s DegreePhD

Industry Keywords

BiotechPharmaceuticalCROClinical TrialsReal-World Data

Tech Stack

Tools & technologies

TableauVBA

About the role

Key responsibilities & impact

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

Requirements

What you’ll need

Bachelor’s degree required, Masters or PhD in 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
Previous experience conducting site feasibility activities in Veeva Clinical or similar site feasibility platform preferred
Demonstrated success in working cross-functionally in a global matrix organization
High proficiency in analysis and data visualization skills/ tools, essential experience with Excel, VBA/macros experience is preferred.
Additional experience with visualization tools such Power Bi, Spotfire, Tableau, statistical analysis/programming, etc.

Benefits

Comp & perks

Medical, Dental, Vision, & Life insurances
Fitness & Wellness programs including a fitness reimbursement
Short- and Long-Term Disability insurance
A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
Up to 12 company paid holidays + 3 paid days off for Personal Significance
80 hours of sick time per calendar year
Paid Maternity and Parental Leave benefit
401(k) program participation with company matched contributions
Employee stock purchase plan
Tuition reimbursement of up to $10,000 per calendar year
Employee Resource Groups participation