Role & Responsibilities
Maintain global oversight of unresolved sample discrepancies for incoming and outgoing shipments
Coordinate with internal teams to resolve discrepancies within defined TAT and OTIF timelines
Perform QC verification of biospecimen data in LIMS and inventory systems
Conduct advanced QC checks and trend analysis on sample data
Support study close-out activities including reconciliation of sample disposition
Monitor patient sample collection schedules and protocol assessment windows
Support study setup activities in LIMS including workflows and protocol configuration
Prepare operational reports including inventory, kit tracking and site performance metrics
Participate in RCA and CAPA activities
Ensure compliance with QMS, SOPs and data privacy regulations
Support ad-hoc analysis and cross-functional operational requests
Qualification
Bachelor’s or Master’s degree in Life Sciences or related discipline
Experience
Minimum 2–3 years of experience in clinical research, sample management or data operations
Skills
Strong understanding of drug, device and biologic development processes
Hands-on experience with clinical databases and LIMS systems
Expertise in data quality and compliance standards
Proficiency in MS Excel, Word, PowerPoint and Outlook
Excellent written and verbal communication skills
Knowledge of GDPR, HIPAA and data privacy regulations
About the Company
Precision For Medicine is a global precision medicine organization supporting international clinical trials, biospecimen management and advanced clinical data operations
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