Study Director - Invitro Metabolism

<h2>Job Overview:</h2><p style="margin-bottom: .0001pt;"><strong><em><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Do you have experience working with invitro metabolism studies such as transporter and phenotyping?</span></em></strong></p><p style="margin-bottom: .0001pt;"><strong><em><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;"> </span></em></strong></p><p style="margin-bottom: .0001pt;"><strong><em><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Are you a Study Director with GLP experience looking to work with a wider variety of clients and studies?</span></em></strong></p><p style="margin-bottom: .0001pt;"><strong><em><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;"> </span></em></strong></p><p style="margin-bottom: .0001pt;"><strong><em><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">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?</span></em></strong></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;"> </span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">If so, then we have the role for you!</span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;"> </span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Labcorp is a leading global life sciences company that includes contract research and developmental services to the </span><a href="https://drugdevelopment.labcorp.com/" target="_blank" rel="noopener"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif; color: windowtext;">pharmaceutical</span></a><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">, </span><a href="http://medtech.labcorp.com/" target="_blank" rel="noopener"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif; color: windowtext;">medical technology</span></a><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">, </span><a href="http://crop-protection.labcorp.com/" target="_blank" rel="noopener"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif; color: windowtext;">crop protection</span></a><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;"> and </span><a href="http://chemical.labcorp.com/" target="_blank" rel="noopener"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif; color: windowtext;">chemical</span></a><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;"> industries.</span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;"> </span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">We are currently recruiting for a Study Director to join our Invitro Metabolism team located in Huntingdon, Cambridgeshire, on a full time, permanent basis. As a Study Director in Invitro Metabolism, you are responsible for managing the design, conduct and reporting of studies to meet scientific, regulatory and client requirements. The Study Director is the single point of study control and has overall responsibility for the scientific, technical and regulatory conduct of studies as well as for the interpretation, documentation and reporting of results. Close and regular liaison with the client is of primary importance.</span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;"> </span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">The main responsibilities will include:</span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;"> </span></p><ul style="margin-top: 0in;"><li style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Act as study director, ensuring studies are performed and reported to high scientific standards</span></li><li style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Supervising studies according to study plans and SOPs in compliance with GLP</span></li><li style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Reviewing and preparing SOPs along with preparing study plans</span></li><li style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Assisting in the evaluation, validation and introduction of new instrumentation or techniques</span></li><li style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Working safely following company and departmental Health and Safety guidelines and local rules in relation to radioactive isotopes</span></li><li style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Interpreting data and preparing reports </span></li><li style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Developing project management skills by effectively managing activities and resources</span></li><li style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Communicating and working with both internal and external customers to provide technical expertise and advice to relevant study staff</span></li></ul><p style="margin-bottom: .0001pt;"> </p><p style="margin-bottom: .0001pt;"><strong><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">We Offer:</span></strong></p><p style="margin-bottom: .0001pt;"> </p><ul style="margin-top: 0in;"><li style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">A competitive salary together with a comprehensive benefits package including health cover and pension</span></li><li style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Unsurpassed career development opportunities supported by exceptional people from across the globe with an energized purpose</span></li><li style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Ability to work with a variety of different, global clients on wide ranging projects</span></li><li style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Relocation package (subject to criteria)</span></li></ul><h2>Education/Qualifications:</h2><ul><li style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">A degree in biology or other relevant scientific subject</span></li></ul><h2>Experience:</h2><ul><li style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">GLP experience in a scientific laboratory environment </span></li><li style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Previous study or project management experience desired</span></li><li style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Great communication and organisational skills</span></li><li style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Experience of working in Metabolism specifically in vitro and/or working with radioactivity [¹⁴C/³H] and analytical techniques including HPLC is advantageous</span></li><li style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Previous data interpretation and report writing experience</span></li></ul>