Program Manager (Reporting, Archiving and Mapping) - Hybrid
Merck
5 months ago
Remote friendly (West Point, PA)
United States
IT
Responsibilities
- Serve as a Subject Matter Expert in Clinical Programming supporting study build, reporting, and analytics; lead process standardization, simplification, and optimization via best practices and continuous improvement.
- Provide technical leadership/oversight for Clinical Programming deliverables across programs, including eCRF review, specifications, protocol understanding, In-Life Report specifications, and library development; ensure compliance with standards/SOPs; manage timelines and escalate risks related to reporting assets and data flow.
- Partner with study teams, leadership, and external vendors to translate study requirements into high-quality solutions; provide clear technical direction and ensure consistency across deliverables.
- Mentor and develop team members; support hiring and performance feedback; ensure standards for development, documentation, and maintenance of libraries.
Qualifications
- BS in computer science (or equivalent software design exposure).
- 7+ years’ experience implementing data transformations/data flow/loading and reporting (e.g., SQL, PL/SQL, Java, DMW/Veeva, Databricks, Python, Legacy SAS; AI tools such as Claude Code).
- 4 years of project management.
- Strong knowledge of eCRF design, clinical databases/data capture and transfer, ETL/reporting tools, and clinical research development process; EDC/DMS knowledge.
- MS Windows/Office and web application exposure.
- Familiar with drug discovery process, FDA/GxP/ICH requirements, clinical database cleaning, and 21 CFR Part 11.
Required/Key Skills
- Accountability, communication, data analysis/quality assurance/validation/reporting, clinical data standards, GCP/GCDMP, mentoring, project management tools, strategic/team management, AI/generative AI.
Preferred Skills
- Current employees/contingent workers apply via the provided links.
Application
- Apply via https://jobs.merck.com/us/en. Posting end date: 04/24/2026 (apply by the day before). Requisition ID: R391665.
Benefits (as stated)
- Eligible for annual bonus and long-term incentive (if applicable) and benefits including medical/dental/vision, 401(k), paid holidays, vacation, and sick/compassionate days.
- Serve as a Subject Matter Expert in Clinical Programming supporting study build, reporting, and analytics; lead process standardization, simplification, and optimization via best practices and continuous improvement.
- Provide technical leadership/oversight for Clinical Programming deliverables across programs, including eCRF review, specifications, protocol understanding, In-Life Report specifications, and library development; ensure compliance with standards/SOPs; manage timelines and escalate risks related to reporting assets and data flow.
- Partner with study teams, leadership, and external vendors to translate study requirements into high-quality solutions; provide clear technical direction and ensure consistency across deliverables.
- Mentor and develop team members; support hiring and performance feedback; ensure standards for development, documentation, and maintenance of libraries.
Qualifications
- BS in computer science (or equivalent software design exposure).
- 7+ years’ experience implementing data transformations/data flow/loading and reporting (e.g., SQL, PL/SQL, Java, DMW/Veeva, Databricks, Python, Legacy SAS; AI tools such as Claude Code).
- 4 years of project management.
- Strong knowledge of eCRF design, clinical databases/data capture and transfer, ETL/reporting tools, and clinical research development process; EDC/DMS knowledge.
- MS Windows/Office and web application exposure.
- Familiar with drug discovery process, FDA/GxP/ICH requirements, clinical database cleaning, and 21 CFR Part 11.
Required/Key Skills
- Accountability, communication, data analysis/quality assurance/validation/reporting, clinical data standards, GCP/GCDMP, mentoring, project management tools, strategic/team management, AI/generative AI.
Preferred Skills
- Current employees/contingent workers apply via the provided links.
Application
- Apply via https://jobs.merck.com/us/en. Posting end date: 04/24/2026 (apply by the day before). Requisition ID: R391665.
Benefits (as stated)
- Eligible for annual bonus and long-term incentive (if applicable) and benefits including medical/dental/vision, 401(k), paid holidays, vacation, and sick/compassionate days.