Senior Director, Scientific Affairs

🕒 May 8

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Logo of ACM Global Laboratories

ACM Global Laboratories

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

ACM Global Laboratories is a leading provider of clinical trial testing services, supporting clinical trials globally in over 65 countries. The company offers a range of bioanalytical services, including small and large molecule analysis, biomarker analysis, and various laboratory testing solutions such as routine safety testing, flow cytometry, and advanced sample tracking. ACM Global Laboratories is recognized for its expertise in bioanalysis and toxicology services, ensuring high sensitivity and accuracy in drug and metabolite measurements across diverse biological samples. The company is dedicated to delivering actionable clinical insights and reliable toxicology services to healthcare providers, partnering with clinical trials to optimize development projects through state-of-the-art laboratory services, specimen management, and global logistics.

📋 Description

• Provide strategic scientific leadership to advance ACM’s long-term vision • Partner with VP Clinical operations to identify and operationalize scientific strategy • Responsible for the performance of the scientific teams by managing resources, prioritizing tasks, and developing and monitoring metrics • Promote a high performing culture through effective talent planning, selection, onboarding, and continuing education • Curate and deliver comprehensive training plans and materials • Provide ongoing coaching and mentorship supported by routine performance metrics • Oversee Principal Scientists and manage strategic initiatives • Coordinate development of 3PL and Client strategy and attend meetings as appropriate • Serve as the point of escalation for internal teams and external clients • Identify and participate in cross functional process improvement initiatives • Oversee and help resolve internal and external audit findings.

🎯 Requirements

• PhD + 10 years in Clinical Trials regulatory laboratory or BS in Life Sciences + 15 years in Clinical Trials regulatory laboratory experience • 5 years of progressive leadership experience • NYS Certification of Qualification through New York State Department of Health, Wadsworth Center • Understanding of Good Clinical Practice (GCP), Good Laboratory Practice (GLP), Good Clinical Laboratory Practice (GCLP) • Application of science in a regulatory environment including validation of methodologies for clinical trials. • Experience leading teams, projects, and troubleshooting essential • Board Certification in relevant areas is preferred.

🏖️ Benefits

• Requires 50% travel to NYS

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