Jobs · Information Technology · North Carolina

Clinical Laboratory Supervisor

Almac Group · Durham, NC · 2 wk ago
Information TechnologyFull-time

About the role

Join Almac as a valued member of our team. We offer a unique culture that delivers exceptional solutions for Biopharma and Biotech industries. Our company is committed to sustainability and operates globally from locations in the UK, US, and Asia.

Responsibilities

  • Contribute to the development and execution of clinical trial supply logistics.
  • Manage inventory levels and ensure timely delivery of materials to clinical sites.
  • Collaborate with cross-functional teams including regulatory affairs, quality assurance, and clinical operations.
  • Ensure compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements.
  • Handle patient randomization and ensure accurate data tracking using Almac ONE™ and other relevant systems.
  • Support the implementation of decentralised trials and manage drug pooling protocols.
  • Provide technical support for eCOA and eConsent processes.
  • Coordinate with external vendors and suppliers to maintain efficient supply chain operations.

Requirements

  • Bachelor's degree in Pharmacy, Biology, Chemistry, or related field.
  • Minimum 3 years of experience in clinical trial supply logistics or related field.
  • Experience with GCP guidelines and regulatory requirements.
  • Strong organizational skills and ability to manage multiple tasks simultaneously.
  • Excellent communication and interpersonal skills.
  • Proficiency in Microsoft Office Suite and familiarity with eCOA/eConsent systems.
  • Qualifications

    • Knowledge of clinical trial supply logistics and regulatory compliance.
    • Experience with patient randomization and data tracking systems.
    • Ability to work independently and as part of a team.
    • Strong problem-solving and decision-making skills.

    Skills

    • Strong understanding of GCP guidelines and regulatory requirements.
    • Experience with eCOA and eConsent systems.
    • Excellent organizational and time management skills.
    • Ability to handle high-volume data entry and tracking.
    • Proficiency in MS Office and relevant software tools.

    Benefits

    • Competitive salary and benefits package.
    • Flexible working hours and remote work options.
    • Professional development opportunities and training programs.
    • Employee wellness programs and support.
    • Regular team-building activities and social events.

    Pay

    Salary range: £XX,XXX - £XXXX per annum.

    Schedule

    Full-time position with standard office hours.

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