Director, Statistical Programming, Clinical Schedules (Hybrid)

Merck · North Wales (upper Gwynedd), PA +1 more

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BiometricsFull-time$191k–$300kCompany career page

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Role summary

Director-level statistical programming leader in biostatistics overseeing clinical schedule management activities for drug and vaccine development programs. Responsible for directing team operations, ensuring quality and compliance across early and late-phase trials, and managing cross-functional partnerships to advance clinical trial capabilities.

What they're looking for

Bachelor's degree in Computer Science, Statistics, Applied Mathematics, Biological Sciences, or Engineering; Master's preferred
12+ years in analysis/reporting environment (BS) or 10+ years (MS)
2 years statistical programming experience in clinical trials
1 year leading and managing a team
7 years project management in statistical analysis and reporting deliverables
Expertise in randomization, clinical schedule specification, and regulatory submissions at leadership level
Strong knowledge of clinical blinding, study design complexities, and regulatory agency requirements

What you'll be doing

Direct clinical schedule managers developing randomization schedules and associated specifications across early and late phase programs
Set direction for clinical schedule management strategy across therapeutic areas ensuring efficient, timely execution with high quality
Manage staff resources, forecast support needs, and oversee hiring and performance development of team members
Partner with Statistics, Data Management, IT, and Clinical Supply teams to enhance schedule management and unblinding capabilities
Lead strategic departmental initiatives and represent clinical schedule management at organizational leadership level

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