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, Labcorp Drug Development'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, Toxicology 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 General Toxicology 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