FREE ACCESS
5,000–10,000 jobs/day

See all jobs on JobTailor
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
About the role
Key responsibilities & impact- Develop and execute supply strategies for IMP/NIMP, ANS, and laboratory samples
- Ensure GLP, GDP, GMP compliance across all participating countries
- Manage project timelines, budgets, and operational resources
- Oversee third-party providers and negotiate contracts
- Conduct risk assessments and develop mitigation plans
- Serve as regulatory point of contact and resolve client issues
- Lead process improvements and system optimization
Requirements
What you’ll need- Strong understanding of GxP regulatory framework
- Extensive pharmaceutical/clinical research/biotech industry experience
- Proven expertise in laboratory and/or clinical trial supply chain management
- Excellent project management and operational leadership skills
- Client-focused approach with strong business acumen
- Financial management and negotiation abilities
- Team mentorship and stakeholder management skills
- Bachelor's degree in biology, pharmacy, health sciences, business administration, or equivalent experience
- Fluent English (written and spoken)
Benefits
Comp & perks- Health insurance
- Paid time off
- Flexible work arrangements
- Professional development
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
supply strategiesGLP complianceGDP complianceGMP compliancerisk assessmentslaboratory supply chain managementclinical trial supply chain managementproject managementfinancial managementnegotiation
Soft Skills
operational leadershipclient-focused approachbusiness acumenteam mentorshipstakeholder management
