Jobs · Project Management · Massachusetts

Site Feasability Manager

Biogen · Cambridge, MA · 1 wk ago
Project Management$122k–$163k/yrFull-time

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.

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.
  • Audit 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, 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.

Preferred Skills

  • Previous experience conducting site feasibility activities in Veeva Clinical or similar site feasibility platform.
  • 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.

Pay

The base compensation range for this role is: $122,000.00-$163,000.00 Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.

Benefits

  • 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.
  • Tuition reimbursement of up to $10,000 per calendar year.
  • Employee Stock Purchase Plan.
  • Employee Resource Groups participation.

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