Biogen

Senior Manager, Clinical Trial Lead

Biogen

full-time

Posted on:

Location Type: Remote

Location: California • United States

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Salary

💰 $131,000 - $175,000 per year

Job Level

Senior

About the role

  • Develops and oversees implementation of the study-level operational strategy for the successful delivery of clinical study(ies)
  • Chairs the SMT to drive the development of scientifically robust, operationally feasible, and clear protocol concepts/protocols
  • Collaborates strategically with the core SMT (study MD, biostatistics, etc.) and other key program team members to provide direction on phase, disease, or therapeutic area to support study design in alignment with the Integrated Development Plan and Global Program Strategy, enabling protocol concept development and driving forward studies through governance approval
  • Leverages operational expertise and scientific assessment to evaluate study feasibility and support protocol development
  • Aligns team perspectives to develop a cross-functional operational strategy, leveraging expertise, current therapeutic knowledge, and relevant supporting data
  • Effectively leads the study via oversight of the CRO, managing performance, quality, and timelines, including defining and delivering against a baseline plan
  • Ensures ongoing data review to identify and mitigate patient safety, study design, data integrity or study conduct issues
  • Exhibit financial management & analysis skills to ensure budgets hold up to appropriate scrutiny and align with study endpoint needs
  • Oversees the delivery of studies by CROs, ensuring quality execution in line with time and budget forecasts
  • Chairs the Study Management Team (SMT) in partnership with the CRO SMT Lead; ensures the CRO creates appropriate risk mitigation plans and is effective in proactively identifying and resolving issues
  • Establishes and drives effective and efficient team operations by setting culture of SMT, ensuring thorough team communication, effective goal setting/management and oversight of strategy implementation
  • Ensures all operational aspects of the study(ies) conduct support patient safety, endpoint integrity and data validity
  • Demonstrates a robust understanding of the study design, rationale, endpoints, and patient population
  • Provides oversight via ongoing review of performance and partnership metrics to ensure key milestones and deliverables are achieved
  • Ensures that all project plans (e.g. Monitoring Plan, Quality Plan, etc.) are in place for effective implementation of studies
  • Leads SMT to develop robust Baseline plans, and ensures team is thoroughly prepared for all key governance forums including but not limited to, Baseline, Study Delivery forum, etc.
  • Proactively & robustly manages inflection points to ensure any necessary course correction is proactively addressed
  • Collaborates with CFP and procurement functions to ensure FMV is achieved and budget oversight responsibilities are met.
  • Maintains data accuracy, completeness and quality within study-related systems (e.g. Clarity, Impact, etc.)
  • Strives for effective, consistent, efficient, and compliant processes
  • Champions best practices and seeks opportunities for innovation and efficiency within CTDU and GCO
  • Seeks synergies and commonalities with other studies, programs, and development units to enhance excellence in study planning and execution
  • Seeks ways to improve and streamline processes to support the GCO CRO outsourcing models; provides feedback via appropriate channels for opportunities to improve processes or establish best practices
  • Embodies a culture of continuous improvement by seeking consistency and efficiency in processes and fully supporting the CRO partnership model
  • Advocates for the CTDU group and actively promotes interaction with other Biogen groups
  • Promotes a rich and diverse knowledge base within CTDU, contributing SME expertise where applicable

Requirements

  • B.A. or B.Sc. in a scientific discipline
  • Scientifically and clinically astute with very strong project management and communications skills
  • Approximately 6 -8 years of clinical operations
  • Clinical Trial/Project Management experience, preferably with both a sponsor company and CRO company, managing outsourced clinical trials within quality, timeline, and budget expectations.
  • Prior investigator site and/or monitoring experience is advantageous
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
  • Employee stock purchase plan
  • Tuition reimbursement of up to $10,000 per calendar year
  • Employee Resource Groups participation
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
clinical operationsproject managementclinical trial managementprotocol developmentdata reviewfinancial managementrisk mitigationstudy designperformance metricsbudget oversight
Soft Skills
leadershipcommunicationcollaborationstrategic thinkingproblem-solvingteam managementgoal settingcontinuous improvementinnovationinterpersonal skills