Study Director, Toxicology

HAR Labcorp Early Development Laboratories Limited; Huntingdon; On-site; GBP 40,000 - 70,000; Full time

Job summary

Labcorp is seeking a Study Director to join our Toxicology Safety Assessment team at our site in Alconbury, Cambridgeshire. This office-based position offers a 37.5-hour work week from Monday to Friday, 08:30–17:00, with responsibilities including study conduct, protocol development, data interpretation and client reporting.

Minimum qualifications include a Bachelor of Science; Master’s degree preferred. Strong knowledge of GLPs, regulatory guidelines and excellent English writing skills are

Qualifications

• 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.

Responsibilities

• Taking responsibility for the technical conduct of a study and reporting of results.
• Developing protocols approved and in compliance with SOPs, GLPs and regulatory guidelines.
• Monitoring progress and status of assigned studies.
• Ensuring accurate recording and verification of all experimental data.
• Direct preparation of reports and submission of results to the client.
• Participating in study-specific client visits.

Skills

Toxicology study design

GLPs

Regulatory guidelines

Communication skills

Problem solving

Interpersonal engagement

English writing

Computers / MS Office

Education

Bachelor of Science

Master of Science

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 Alconbury, 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.

We believe in the power of science to change lives. Labcorp is a leading global life sciences company that provides vital information to help doctors, hospitals, pharmaceutical companies, researchers, and patients make clear and confident decisions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations to improve health and improve lives. Here, you can join our nearly 70,000 employees, serving clients in more than 100 countries, as we work together to transform approaches to patient care.