Study Director

Labcorp; St. Neots; On-site; GBP 60,000 - 90,000; Full time

Job summary

Labcorp is seeking a Study Director to join our Toxicology Safety Assessment team at our site in Huntingdon, Cambridgeshire. This office-based role is 37.5 hours per week, Monday to Friday, with responsibilities spanning study conduct, protocol development, data interpretation, and client reporting.

A BSc is required; MSc preferred. Applicants should have strong knowledge of GLPs, regulatory guidelines, and excellent written and verbal English skills.

Qualifications

• Bachelor of Science degree in a related field.
• Master's degree preferred.
• Solid knowledge of GLPs and regulatory guidelines.
• Strong English writing and communication skills.

Responsibilities

• Take responsibility for the technical conduct of a study and report results.
• Develop protocols compliant with SOPs, GLPs, and regulatory guidelines.
• Monitor progress and status of studies.
• Ensure data accuracy and verification of observations.
• Prepare reports and submit results to the client.
• Participate in study-specific client visits.

Skills

Toxicology knowledge

GLP compliance

Study design

Regulatory guidelines

Communication skills

Education

Bachelor of Science degree

Master of Science degree

Tools

Microsoft Office

Job description

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives.

Labcorp is seeking a Study Director to join our Toxicology Safety Assessment team at our site in Huntingdon, Cambridgeshire.

Work Schedule: 37.5 hours per week, Monday - Friday, 08:30 - 5pm

Job Responsibilities:

• Taking responsibility for the technical conduct of a study in addition to the interpretation, analysis, documentation and reporting of results
• Developing protocols and ensuring that the protocol, including any changes, is approved and is in compliance with appropriate SOPs, GLPs, and regulatory agency guidelines
• Monitoring progress and status of assigned studies
• Ensuring that all experimental data, including observations of unanticipated responses to the test system, are accurately recorded and verified
• Direct preparation of reports, interpreting results and ensuring compliance with the protocol and regulatory requirements, and submitting results to the client
• Participating in study-specific client visits

Minimum Qualifications:

• Bachelor of Science degree

Preferred Qualifications:

• Master of Science degree

Additional Job Standards:

• Knowledge of toxicology study design and conduct in adherence to regulatory guidance
• Strong customer service skills
• Knowledge in planning, negotiation and process innovation
• Demonstrated ability to interact effectively with all staff and management levels
• Demonstrated problem solving and decision-making skills
• Advanced knowledge of GLPs and regulatory agency guidelines
• Strong English writing and communication skills
• Advanced knowledge of computers and programs (e.g., word processing and spreadsheet applications)

This is an office-based position

Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.

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