Study Director - Development and Reproductive Toxicology

Have you got experience in Development and Reproductive Toxicology (DART) or in vivo Study Direction and are you looking to progress up the career ladder?

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'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 DART team at our site in Harrogate, North Yorkshire. 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!