LabCorp
Harrogate, United Kingdom
Job Responsibilities include:
- Lead scientific activities supporting method development, validation, and sample analysis projects
- Serve in key study leadership roles (e.g., Study Director, Principal Investigator, Responsible Scientist) for regulated and non-regulated studies.
- Develop, review, and approve protocols, validation plans, reports, and study data.
- Provide scientific oversight to ensure compliance with GLP, GCP, regulatory, and client requirements.
- Act as the primary scientific contact for clients, defining project requirements and managing scientific expectations.
- Identify and resolve scientific challenges, risks, and scope changes throughout the study lifecycle.
- Provide technical expertise and support assay troubleshooting and scientific investigations.
- Lead, mentor, and develop scientific staff while fostering collaboration and a culture of quality.
- Manage multiple complex projects, ensuring delivery to quality, timeline, and client expectations.
- Drive continuous improvement initiatives that enhance scientific excellence and client satisfaction.
Minimum Qualifications:
- Bachelor's degree (or equivalent experience) in a relevant scientific discipline.
- Significant experience in bioanalytical method development, validation, and regulated study conduct within a Contract Research Organization (CRO) environment.
- Previous experience as a Study Director (SD), Principal Investigator (PI), and/or Responsible Scientist (RS) is required for regulated bioanalytical studies.
- Thorough understanding of GLP, GCP, and applicable global regulatory requirements governing bioanalytical studies.
- Proven ability to interpret complex scientific data, troubleshoot technical issues, and make sound scientific and regulatory decisions.
- Excellent client management, communication, and stakeholder engagement skills, with experience building and maintaining successful customer relationships.
- Demonstrated leadership, mentoring, and project management experience, including oversight of scientific staff and management of multiple concurrent projects.
- Ability to manage a high-volume workload while maintaining scientific quality, regulatory compliance, and exceptional attention to detail.
The Lead Scientist is responsible for the management of bioanalytical (LC-MS/MS) studies/phases of studies and to ensure that all work is conducted in accordance with the Study Plan, SOPs and appropriate regulatory standards such as GLP & GCP, and guidelines (EMA and FDA Bioanalytical Method Validation, SANTE etc.). To run on a day to day basis and report, studies of various types and complexity.
We are looking for a strategic scientific leader with strong technical expertise, a customer-focused mindset, and a passion for delivering high-quality science while developing teams and building strong client partnerships.
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