When our values align theres no limit to what we can achieve.
At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us no matter what we do at Parexel contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally we do it with empathy and were committed to making a difference.
Are you ready to lead impactful projects ensuring secure timely patient treatment in clinical trials
Were seeking an experiencedClinical Trial Supply & Project Leader to provide global leadership in clinical and laboratory supply chain management.
Youll combine clinical/lab supply expertise with client understanding to develop optimal solutions ensuring operational excellence quality standards and regulatory compliance.
HIRING LOCATIONS
This role is open to candidates based in:Serbia Poland Lithuania Czech Republic Hungary
You must be legally authorized to work in one of these countries.
Key Responsibilities
- 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
Essential Requirements
- 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
- Bachelors degree in biology pharmacy health sciences business administration or equivalent experience
- Fluent English (written and spoken)
What Makes You Stand Out
- Multinational work experience
- Creative problem-solving in clinical supply chains
- Proficiency in MS Office Suite
Join our innovative dynamic international organization and make a significant impact in clinical trial operations.Apply now!
Required Experience:
Senior IC
When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in...
When our values align theres no limit to what we can achieve.
At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us no matter what we do at Parexel contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally we do it with empathy and were committed to making a difference.
Are you ready to lead impactful projects ensuring secure timely patient treatment in clinical trials
Were seeking an experiencedClinical Trial Supply & Project Leader to provide global leadership in clinical and laboratory supply chain management.
Youll combine clinical/lab supply expertise with client understanding to develop optimal solutions ensuring operational excellence quality standards and regulatory compliance.
HIRING LOCATIONS
This role is open to candidates based in:Serbia Poland Lithuania Czech Republic Hungary
You must be legally authorized to work in one of these countries.
Key Responsibilities
- 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
Essential Requirements
- 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
- Bachelors degree in biology pharmacy health sciences business administration or equivalent experience
- Fluent English (written and spoken)
What Makes You Stand Out
- Multinational work experience
- Creative problem-solving in clinical supply chains
- Proficiency in MS Office Suite
Join our innovative dynamic international organization and make a significant impact in clinical trial operations.Apply now!
Required Experience:
Senior IC
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