Director, Global Clinical Process Management Lead
$171,900–$231,900 year
RemoteUnited States
Job Summary
Drive global clinical process management activities within GCO, ensuring processes and standards are efficient, consistent, sustainable, and compliant with regulatory requirements. Serve as the primary point of contact for assigned processes, including SOPs, work instructions, and standards, while leading document review and approval workflows. Collaborate with Global Process Owners and Subject Matter Experts to develop procedural content, assess regional feedback, and translate process changes into practical business implications for adoption. Act as a liaison between Regional Heads and the GCPM team to consolidate insights, escalate concerns, and mentor Associate Directors to support capability development and consistent process leadership.
Required Qualifications
- Fluent English (Oral; Written)
- Relevant bachelor's degree minimum
- Minimum of 8 years of experience in pharmaceutical and/or biotechnology sector
- Extensive knowledge of clinical operations process, ICH-GCP and compliance management
- Experience in clinical trial process design, harmonization/optimization and implementation
- Experience working in matrix environment and in global teams
- Excellent interpersonal, problem-solving, negotiation and conflict resolution skills
- Excellent organizational skills and a pre-disposition to quality management and process improvement
- Effective communicator (oral and written)
- Strong presentation skills
- Bachelor's degree required
- Master's or other relevant post graduate qualification preferred
Desired Qualifications
- Relevant bachelor's degree minimum – preferred science/healthcare discipline
- Master's or other relevant post graduate qualification preferred
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