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Covance
,
Harrogate, North Yorkshire
Study Director - Toxicology
Overview
Job Description
Job Overview: 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'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 Toxicology department at out 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 * 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 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 Employment Type: Full Time