Jobs · Analyst · Kentucky

Senior Director, Scientific Affairs

ACM Global Laboratories · Headquarters, KY · 2 mo ago
Analyst$175k–$240k/yrFull-time

Responsibilities

  • 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 and uphold a high performing culture through effective talent planning, selection, onboarding, and continuing education
  • Curate and deliver comprehensive training plans and materials to foster successful onboarding and employee performance
  • Provide ongoing coaching and mentorship supported by routine performance metrics to identify clear performance feedback and career development plans
  • Foster professional development through continuous coaching and performance management
  • Oversee Principal Scientists and works with key operational and regulatory leadership for strategic initiatives including new biomarkers and technologies
  • Oversee and manage the R&D team to assign resource in line with required validations and laboratory support of safety testing
  • Collaborates with VP, Clinical Operations to create plans for conference attendance and external marketing
  • Serve as the point of escalation to provide scientific solutions as required for internal teams and external clients
  • Identify, lead, and/or participate in cross functional process improvement initiatives to optimize capabilities
  • Collaborates in the development of 3PL and Client strategy and attends meetings as appropriate
  • Assign Principal Scientist team to support non-safety testing aspects to expand service offerings and provide scientific expertise for 3PL assignment and regulatory audits
  • Assign R&D team to support safety testing to expand service offering and provide expertise for client and 3PL safety enquiries
  • Oversee and help resolve internal and external audit findings
  • Perform other duties as needed
  • 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

    Qualifications

    • NYS Certification of Qualification through New York State Department of Health, Wadsworth Center in: Clinical Chemistry, Diagnostic Immunology, Endocrinology, and/or Hematology
    • Understanding of Good Clinical Practice (GCP), Good Laboratory Practice (GLP), Good Clinical Laboratory Practice (GCLP), College of American Pathologists (CAP), NYSH and UK EMEA

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