Study Director - Development and Reproductive Toxicology
- Employer
- Labcorp
- Location
- Eye, United Kingdom
- Salary
- Competitive
- Start date
- 3 Oct 2022
- Closing date
- 2 Nov 2022
View more
- Discipline
- Clinical Research
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
Do you want the opportunity to work for a global organization who strive to make a difference to people's everyday lives by bringing essential products to the market?
Are you at a stage in your career where you are ready to work on a variety of studies with differing levels of complexity?
As one of the world's premier Contract Research Organizations, Labcorp Drug Development'smission is to help build a healthier and safer world by providing research services for a multitude of our customers.
We are looking for a Study Director to work in our DART team at our site in Eye, Suffolk. This is to be responsible for, to organise, to run on a day to day basis and report, studies of various types and complexity.
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 including monitoring progress and status
- Developing protocols and ensuring that the protocol, including any changes, is approved and is in compliance with appropriate SOPs, GLPs, and regulatory agency guidelines
- 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 as required
We offer:
- Competitive salary and benefits package
- Unparalleled opportunities for career development and progression within a global organisation with global clients
- Excellent relocation package (subject to criteria)
- Flexible working arrangements
Education:
- BSc minimum preferably in life science (MSc/PhD preferred) or equivalent industry experience
Skills / Experience:
- Experience working as a Study Director to GLP standards
- Knowledge and/or experience in performing a number and/or complexity of DART studies along with study design and conduct in adherence to regulatory guidance
- Strong customer service and communication skills
- Knowledge in planning, negotiation and process innovation
- Demonstrated problem solving and decision-making skills
If you are looking to make a difference and want to work within a supportive team, where there are real opportunities to learn, develop and progress then we would like to hear from you!
Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.
For more information about how we collect and store your personal data, please see our Privacy Statement .
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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