Merck
Technical Project Manager
CRI - San Jose - San Jose (City Place) · Contract
Sponsorship not specifiedDetected 67 days ago
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Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70
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About the role
- The Technical PM is responsible for the end-to-end project management and delivery of technical deliverables for assigned clinical trials within a specific drug/vaccine program.
- Represents Global Clinical Data Integration (GCDI) on cross-functional Global Data Management project teams.
- Participates in the development of, and ensures adherence to, Company's clinical data management procedures.
Responsibilities
- Build and maintain detailed plan for design, build, testing, deployment, run, and closeout of study-level technical deliverables (e.g., eCRFs, data-collection systems, integrations, edit checks/derivations, listings/reports, archival/decommissioning)
- Lead discovery with study stakeholders/SMEs to assess complexity, define technical requirements and inputs/timelines, and confirm the full set of data-management services
- Ensure appropriate use of standards and project-level consistency in database design, data collection, and validation
- Orchestrate configuration and build of study-level technical deliverables with full traceability to requirements
- Triage defects and manage change requests with stakeholders and vendors
- maintain audit-ready documentation throughout the study lifecycle
- represent GCDI on cross-functional teams and partners, facilitating decision making
Requirements
- No Travel Required
Nice to have
- PM certifications are preferred
- Experience facilitating data migration and integration from different sources preferred
- Preferred Skills:
Skills
- Working knowledge of clinical data management systems
- Awareness of data standards and data flow principles
- Strong project management skills (planning, execution, change control, RAID management, escalation)
- Strong organization and leadership skills
- Current Employees apply HERE
- Current Contingent Workers apply HERE
- Search Firm Representatives Please Read Carefully
- Where agency agreements are in place, introductions are position specific.
- Please, no phone calls or emails.
- Employee Status:
- No relocation
- VISA Sponsorship:
Company info
- Participates in the development of, and ensures adherence to, Company's clinical data management procedures. Interacts with staff across multiple Company's sites and external vendors.
- Interacts with staff across multiple Company's sites and external vendors.
Visa & Work Authorization
- VISA Sponsorship:
This listing is sourced directly from Merck's careers page and normalized into a canonical job model.