Largo, Maryland
Largo, Maryland
Martinsville, Indiana
Posted: 27-Feb-25
Location: Huntingdon, United Kingdom
Type: Full-time
Categories:
Internal Number: 255578
Are you looking for a scientific position where you can utilise your customer service and project management skills?
Do you enjoy inspiring others and leading by example?
If so, read on!
Recognized as one of Forbes? World?s Best Employers 2024 and named one of The World?s Most Admired Companies 2025 by Fortune, Labcorp is seeking to hire a Study Director within our Cardiovascular Safety Pharmacology team based at our site in Huntingdon, Cambridgeshire.
Serving as Study Director on cardiovascular pharmacology studies you will perform tasks according to the protocol/study plan, Standard Operating Procedure(s), and to the highest possible scientific standards. In this role, you will have overall responsibility for the conduct of a study, coordinating efforts of the study team, leading the interpretation, analysis, documentation and reporting of results. Activities also include productive interactions with management, technical staff, global internal and external clients, and study direction staff.
The ideal candidate will preferably have prior experience as a Study Director in a GLP environment, although candidates with suitable background, potential and motivation can be considered. Minimum education requirement is MSc or equivalent in a related field but PhD preferred.
Duties Include:
To Study Direct pre-clinical safety pharmacology work according to the Study Plan, Standard Operating Procedure(s) (SOP) and to the highest possible scientific standards
To liaise with Sponsors and other customers in a timely and professional manner on study related matters
To maintain accurate records of all laboratory work performed, in accordance with the standards of Good Laboratory Practice (GLP)
Perform studies according to the Study Plan, Standard Operating Procedure(s) (SOP), the principles of Good Laboratory Practice (GLP) and high scientific standards
Accurately collate the data generated during studies
Prepare reports for studies and submit for review by line manager
Maintain study and report dates and other agreed information on the Master Schedule
Perform and/or provide technical assistance for validation studies
Comply with the United Kingdom Animals (Scientific Procedures) Act 1986 (the Act) and other Acts as required
To provide excellent customer care to both internal and external clients
To deliver a professional, quality service to each customer, including timely production of high quality study plans and reports
Maintains an up-to-date knowledge and understanding of the industry position on related pharmacology disciplines to provide credibility and confidence to clients.
We Offer:
Competitive salary and benefits package including health cover and contributory pension
Ability to work with a variety of different clients on wide ranging projects/studies
Excellent relocation package (subject to criteria)
Flexible/Hybrid working arrangements available after training and subject to critical phases of the studies
A culture of CARE with access to well-being programs and various employee resource groups
Skills / Experience:
Ideally with a CRO background, you will have experience working effectively as a Study Director to Good Laboratory Practice (GLP) standards. Cardiovascular experience is preferred
Ability to work to regulatory requirements
Strong customer service, data interpretation and report writing skills
Excellent attention to detail with great accuracy
If you want to work within a growing and supportive team whilst making the most of your scientific and regulatory expertise then apply now!
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. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.
We encourage all to apply
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