Associate Study Director - Safety Pharmacology
- Employer
- Labcorp
- Location
- Huntingdon, United Kingdom
- Salary
- Competitive
- Start date
- 14 Jul 2021
- Closing date
- 3 Aug 2021
View more
- Discipline
- Medical Affairs, Scientific Advisor
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
Do you have a BSc or experience directing studies?
Are you interested in Cardiovascular Safety Pharmacology?
Do you want the opportunity to work on a variety of studies within a global organization?
If the answer is YES then the Cardiovascular Safety Pharmacology team at Labcorp Drug Development , Huntingdon can offer you the opportunity to work and develop within a supportive and growing environment!
As one of the world's premier Contract Research Organizations, Labcorp Drug Development's mission is to help build a healthier and safer world by providing research services for a multitude of our customers.
As an Associate Study Director working on cardiovascular safety pharmacology studies you will learn overall responsibility for the technical conduct of a study, coordinate efforts of the study team and lead the interpretation, analysis, documentation and reporting of results.
As an Associate Study Director, the main responsibilities will include:
- Liaising with internal and external customers to ensure prompt and proper action on all aspects of the study plans for studies assigned
- Taking ownership of the day to day organization, analysis and reporting of various studies
- Attending and, where appropriate, assisting in key elements of the work of assigned studies
- Accurately collating the data generated during studies
- Performing and/or providing technical assistance for validation studies
- Maintaining an up-to-date knowledge and understanding of the industry position on cardiovascular safety pharmacology in general and in vitro assays in particular to provide credibility and confidence to clients
What Labcorp Drug Development can offer you:
- A competitive salary together with a comprehensive benefits package including health cover and pension
- Unsurpassed career development opportunities supported by exceptional people from across the globe with an energized purpose
- Ability to work with a variety of different, global clients on wide ranging projects
- Flexible working
- Relocation package (subject to criteria)
Labcorp Drug Development has helped pharmaceutical and biotech companies develop one-third of all prescription medicines in the market today so if you want to be part of a team that helps to bring the miracles of medicine to market sooner then please apply now.
Education/Qualifications:
- Master'sand/or Bachelor's degree in Life Sciences, toxicology or Safety Pharmacology preferred
- Ideally with a CRO or pharmaceutical background, you will have demonstrable experience in conducting research, data interpretation and writing reports effectively either as a Study Director or from relevant scientific laboratory work
- Strong customer service and report writing skills
- Excellent attention to detail with great accuracy
- Previous experience working to Good Laboratory Practice (GLP) in desirable
Company
At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions —because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us in our pursuit of answers.
- Website
- https://careers.labcorp.com/global/en
- Location
-
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom
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