Senior Director, Head of Feasibility, Americas

BeiGene

130d • $202,200 - $272,200

About The Position

As the Regional Strategic Feasibility Lead Senior Manager within Global Clinical Operations (GCO), you will play a vital role in collaboration with the global strategic feasibility lead, study teams, and cross-functional stakeholders in the region to deliver data-driven strategic feasibility reports for early to late-stage medicines development. Your responsibilities will encompass site identification and recruitment and retention recommendations, ensuring the successful execution of clinical trials from concept to completion.

Requirements

• Bachelor’s degree (or equivalent) or higher in a scientific, medical or healthcare discipline.
• Minimum of 12 years of combined experience in Feasibility, Clinical Trial Management, Personnel Management and Operations Management.
• Experience with trial optimization vendors, tools, and methods.
• Proficiency with software models and database structures.
• Expertise in principles driving country/site identification, feasibility, and study startup strategies.
• Validated experience in data analysis, data interpretation to drive inform decision making.
• Experience in managing, influencing, building, and managing relationships and achieving results with senior partners in conflicting priority environment.
• Experience or willingness to learn how developing study delivery strategies and tactical/operational plans aligned to commercial and regulatory objectives.
• Clinical trial patient and investigator recruitment experience.
• Validated experience in project and budget management.
• Confirmed experience working with Global teams.

Responsibilities

• Act as the primary point of contact for the Global Strategic Feasibility and Regional Clinical Operations teams for Feasibility and Re-Feasibility activities.
• Liaise cross-functionally to expedite and predictively deliver feasibility insights at various levels (TA, indication, program, study), ensuring standardization of data, tools, and processes for quality decision-making.
• Combine and integrate data from internal stakeholders and external sources to provide clear feasibility strategies for site identification, recruitment, and retention at the TA/indication/program level.
• Utilize comprehensive data analysis, including local treatment standard of care, disease prevalence, drug landscape, and historical trial data, to inform protocol development and establish geographic footprints and proposed sites for participation in clinical studies.
• Utilize competitive intelligence data to develop accurate study startup forecasts, benchmark assumptions, and enrollment plans.
• Maintain patient enrollment forecasts strategically, adjusting for new influencing factors and developing risk mitigation plans.
• Lead the design and implementation of study-specific recruitment programs, collaborating with study teams, vendors, and CROs as needed to optimize participant recruitment.
• Implement creative processes, methodologies, data, and technologies to enhance the delivery of Feasibility and Study Startup Services.
• Contribute to ongoing strategic planning, capability assessments, and training efforts to ensure successful feasibility support.
• Perform root cause analysis and develop mitigation strategies to address study execution and enrollment challenges.
• Participate in regional and global projects, representing Clinical Operations and Study Optimization to support BeiGene R&D goals.
• Drive high level of ownership and accountability within team and with external stakeholders.
• Line Manage - Country Feasibility and Clinical Trial Diversity teams.

Benefits

• Medical
• Dental
• Vision
• 401(k)
• FSA/HSA
• Life Insurance
• Paid Time Off
• Wellness
• Annual bonus plan for non-commercial roles
• Incentive compensation plan for commercial roles
• Discretionary equity awards
• Employee Stock Purchase Plan

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Bachelor's degree