Description
ICON is seeking a Supervisor, Bioanalytical Services - Flow Cytometry to join their team. In this role, you will serve as the operational lead for assigned studies, overseeing study execution, timelines, scheduling, inventory management, resource allocation, and study-related communications.
Responsibilities:
- Serve as the operational lead for assigned studies, providing oversight of study execution, timelines, deliverables, and overall study performance.
- Coordinate study scheduling, inventory management, resource planning, and laboratory workflows to ensure project milestones and client expectations are achieved.
- Partner closely with laboratory analysts to ensure run packets, testing activities, and study deliverables are completed accurately and within established timelines.
- Monitor study progress and proactively address operational challenges to support successful project execution.
- Participate in study-related meetings and provide project updates and operational support as needed.
- Coordinate daily laboratory activities and workload assignments to ensure efficient utilization of resources.
- Ensure compliance with SOPs, GxP requirements, quality standards, and client expectations.
- Maintain inspection readiness and support quality and compliance initiatives within the laboratory.
- Identify and implement process improvement opportunities that enhance operational efficiency, quality, and client satisfaction.
- Collaborate with cross-functional teams to ensure successful study execution and delivery of client commitments.
- Provide leadership, coaching, training, and performance management support for a team of approximately 4-5 direct reports.
- Foster a culture of accountability, continuous improvement, collaboration, and scientific excellence.
Your Profile:
- Minimum of 3 years of hands-on Flow Cytometry experience required.
- Experience working within a CRO, bioanalytical, pharmaceutical, clinical research, or other regulated laboratory environment.
- Demonstrated experience leading studies, projects, laboratory operations, or other operational activities.
- Experience with study scheduling, resource planning, inventory management, and workflow coordination.
- Strong understanding of GxP regulations, quality systems, and regulated laboratory operations.
- Excellent organizational, problem-solving, and communication skills.
- Ability to manage multiple priorities and deadlines in a fast-paced environment.
- Bachelor's degree in Biology, Biochemistry, Clinical Laboratory Science, or a related scientific discipline preferred. Associate degree with relevant experience will be considered.
Rewards & Benefits:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways