Location: America
Engagement Status: Contract (Ongoing)
We are partnered with a leading global biotechnology company who is looking for a Process Improvement Manager to provide BAU support to the Clinical Development Operations. This role focuses on process coordination, SOP management, and continuous improvement within a regulated clinical development environment.
Key Responsibilities
- Own and maintain Clinical Development SOPs and procedural documentation
- Coordinate documentation updates following:
- Process changes
- CRO procedural updates
- New or updated regulations
- Ensure processes and documentation are controlled, compliant, and inspection ready
- Identify and support practical process improvements with process owners
- Coordinate training activities linked to procedure changes (no training design)
- Act as a key contact for CROs to ensure procedural and process alignment
- Support inspection and audit readiness activities with Quality and Clinical Ops
Requirements
Hard Skills
- Process management and continuous improvement experience
- Coordination of SOPs and procedural documentation
- Experience in regulated pharma or biotech environments
- Understanding of how regulatory changes impact processes
- Exposure to Clinical Development Operations
- CRO interface and procedural alignment experience
- Inspection / audit readiness exposure
- Quality or Quality Systems exposure
Soft Skills
- Strong stakeholder coordination and communication skills
- Highly detail‑oriented and organised
- Comfortable supporting BAU operations
- Practical, hands‑on approach
- Confident working across global, cross‑functional teams
Education
- Degree in life sciences or related discipline preferred
- Equivalent industry experience considered
This role is not clinical trial delivery, learning design, or large-scale transformation.
Job Type: Contract
Job Location: USA
Salary: Competitive