Covance

Study Director - Development and Reproductive Toxicology

Company
Covance
Location
Eye, United Kingdom
Salary
Competitive
Posted
11 May 2021
Closes
17 May 2021
Ref
10024_64436
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Are you at a stage in your career where you are ready to work on a variety of studies with differing levels of complexity?

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?

As one of the world's premier Contract Research Organizations, Covance by Labcorp's mission 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 Study Direction department at our site in Eye, Suffolk.This is to be responsible for, to organise, to run on a day to day basis and report, DART 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
  • 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 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


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!
Education/Qualifications:
  • BSc minimum preferably in life science (MSc/PhD preferred) or equivalent industry experience
Experience:
  • Experience working as a Study Director to GLP standards
  • Knowledge and/or experience in performing a number and/or complexity of safety assessment 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

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