Are you proactive, enjoy working with people and have a keen interest in science?
Are you looking to take the next step in your career? Or maybe a career change?
Labcorp Drug Development are looking for individuals interested in joining our Safety Assessment Study Coordination team as a Senior Study Coordinator (Trainee Study Director) at our site in Alconbury, Cambridgeshire. This could be worked as a hybrid role where following a period of training there would be the opportunity to work from home for 2/3 days per week (averaged over a month).
The Senior Study Coordinator is responsible for working closely with the Study Director to coordinate the activities of routine and non-routine toxicology studies, in compliance with the appropriate company standards, Home Office requirements and regulatory guidelines, in a timely, efficient manner. A comprehensive training program is available to provide development into various roles including Study Director, Program Management and even people management roles.
The Study Coordinator:
Provides scientific and administrative support for assigned toxicology studies from award, through the in-life phase. This involves multiple study set up tasks including protocol development, scheduling and initiation meetings
Proactively liaises with Study Directors, clients, study monitors, Principal Investigators and internal departments to ensure accurate and timely protocol and amendment development and distribution
Learns about all aspects of safety assessment toxicology studies and the drug development process
Works with key clients and learns to implement action plans for solving study problems as they occur, including participation in client issue resolution process and any associated internal or external discussion
Co-hosts or independently hosts client visits. May also assist with regulatory visits as appropriate
Possesses the ability to mentor and train less experienced staff members
May work with global or regional teams on projects and opportunities
What Labcorp Drug Development can offer you:
Exposure to a variety of studies and the opportunity to interact with all departments involved in pre-clinical toxicology studies from client managers to reporting teams
Competitive salaries and a comprehensive benefits package including health cover and contributory pension
Unrivalled opportunities to develop a successful career in the scientific industry
Unsurpassed learning and career development opportunities where you can learn as you develop in a supported team environment
Flexible working with the possibility of remote working some of the time
BSc, a Life Science degree preferred. Experience may also be substituted for education
Skills and experience:
Demonstrable experience in an associated role such as Toxicology operations, Project Management or a customer/ client facing role
Demonstrates excellent communication and time management skills
Excellent attention to detail and consistent accuracy whilst managing multiple changing priorities
Knowledge of GLPs, regulatory agency guidelines and Home Office requirements is desirable
Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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. We encourage all to apply.
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