Global Clinical Process Management Senior Specialist
Employment type
Full-time
Work setting
On-site
Location
Emeryville, CA
Schedule
Day shift
Posted
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Job overview
The Global Clinical Process Management Senior Specialist role is onsite in Emeryville, CA. Compensation is not specified. The role provides operational support to Process Leads and senior Global Clinical Process Management (GCPM) leadership. The position coordinates document governance, project tracking, reporting, and intake analysis so GCPM initiatives can progress consistently and support timely decisions. It helps maintain process oversight and continuous improvement through organized information, approval workflows, and management reporting.
What you'll do
- Support document review and approval workflows and coordinate document control activities, including QA alignment and tracking approvals.
- Gather and organize inputs, maintain project plans and stakeholder materials, and assist with change-management communications.
- Compile source-system data for status reporting, maintain QE CAPA tracking materials, and analyze GCPM intake data for management review and process improvement.
What we're looking for
- Skills & competencies
- global clinical process managementsenior specialistclinical processesdocument controlgcpmich-gcpprocess improvementproject plansstatus reportingemeryville cabeone medicines
- Work arrangement
- Weekend coverage required
Why this role
Bachelor’s degree required; pharmaceutical or biotechnology experience preferred. Knowledge of ICH-GCP is listed.
About the employer
BeOne Medicines is hiring for this role. Industry: Pharmaceutical Preparation Manufacturing. Sector: 32.
Additional details
- Industry sector
- 32
- Industry
- Pharmaceutical Preparation Manufacturing
- Occupation code
- 15-2051.02
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Listing ID: e7d570c1-f6f0-4bdf-87f0-e2cdd374e277