Study Director

Company description: At Labcorp Drug Development we believe in the power of science to change lives. Labcorp is a leading global life sciences company that provides vital information to help doctors, hospitals, pharmaceutical companies, researchers, and patients make clear and confident decisions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations to improve health and improve lives. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to transform approaches to patient care. Job description: Do you have an Analytical Chemistry background? 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 organisation 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 Organisations, 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 Dose Analysis department at our site in Huntingdon, Cambridgeshire. This role 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: Liaise with the Team Leaders and Head of Department for the planning, supervision and reporting of Inhalation and Formulation Analysis data. Ensure that all data produced by designated staff is in accordance with Protocol, GLP and relevant SOPs. Undertake the role of Study Director for standalone Dose Formulation Analysis studies. Taking ownership of the day to day organisation, 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. Method development and validation. 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. Required profile: Education/Qualifications: BSc (Hons) in (Bio)Chemistry or equivalent subject. Experience: Educated to degree level in Chemistry (or equivalent is essential) Previous work/study experience in a laboratory is essential and the desire to work in a scientific environment Proven ability to build relationships with clients, scientists and related departments is desirable Knowledge or experience of working in a GLP regulated environment Knowledge or experience of using HPLC analysis This role can be made available as a Trainee Study Manager role too What 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). 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

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