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Global brand plus a common project management title increases applicant density, moderated by junior level and clinical niche.
Clinical trials, GMP/GxP, and pharma supply chain focus make background fit highly industry-specific.
Explicit 1+ year requirement and GMP/clinical supply chain expectations cause moderate shortlisting strictness.
Manage and coordinate clinical trial project documentation and supply chain activities to ensure timely and quality service delivery.
Collaborate with internal teams and clients to support successful study execution and maintain adherence to GMP/GxP standards.
Plan projects, handle multiple simultaneous projects, and ensure cross-functional alignment to meet client expectations.
Bachelor's degree in healthcare, supply chain management, life sciences, or related field.
Minimum 1 year of experience, preferably in clinical trials material services or pharmaceutical industry.
Strong understanding of GMP/GxP principles and quality management systems.
Advanced proficiency in Microsoft Office (Excel and Project); experience with Salesforce, GPMS, and TrackWise preferred.
Experienced in managing multiple clinical trial or pharmaceutical projects with demonstrated project management skills.
Comfortable working independently and collaboratively across cross-functional teams in regulated environments adhering to GMP/GxP standards.
Strong analytical, organizational, and communication skills to effectively manage stakeholder relationships and deliver quality service under changing priorities.