Senior Study Manager - LCMS/MS

<h2>Job Overview:</h2><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>Are you looking for your next opportunity in Bioanalysis (LC-MS/MS) Study Management?</strong></span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong><span style="font-size: 12pt;"><span style="font-family: Arial, sans-serif;">Are you at a stage in your career where you are ready to work on a variety of studies with differing levels of complexity?</span></span></strong></span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>Do you want to be the pivotal point between our clients and scientists?</strong></span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>Do you want to work for a world class leading company who work together to build a healthier and Safer world?</strong></span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">If this sounds like you, Covance by Labcorp is looking for a Senior Study Manager to join our growing Bioanalysis (LC-MS/MS) team in Alconbury,  Cambridgeshire.  </span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Covance by Labcorp provides essential products and research services for pharmaceutical, crop protection, chemical companies, universities, governments, research organisations.</span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">The <strong>Senior Study Manager</strong> is responsible for the management of bioanalytical (LC-MS/MS) studies/phases of studies in the capacity of a Study Director, Project Manager, Responsible/Contributing Scientist or Principal Investigator. Ensure that all work is conducted in accordance with the Study Plan, SOPs and appropriate regulatory standards such as GLP & GCP, and guidelines (EMA and FDA Bioanalytical Method Validation, SANCO etc.).  T<span style="font-size: 12pt; font-family: Arial, sans-serif;">o run on a day to day basis and report, studies of various types and complexity.</span></span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>As a Senior Study Manager your main responsibilities will be:</strong></span></p><ul><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Direct the successful commencement, running, completion, reporting and archiving of studies assigned to them</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">To liaise with internal and external customers to ensure prompt and proper action on all aspects of the study plans for studies assigned. To attend and, where appropriate, assist in key elements of the work of assigned studies</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">To maintain an awareness and familiarity with other studies assigned to the team so that continuity may be achieved in the absence of any member of the team</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Develop and maintain sufficient experience in bioanalytical extraction (protein precipitation, SPE, liquid-liquid, etc) techniques and use of instrumentation (LC-MS/MS, robotics, etc) such that is not a limiting factor in supporting the Study Managers</span></li></ul><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>What Covance by Labcorp can offer you:</strong></span></p><ul><li style="margin-left: .25in;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Competitive salaries and a comprehensive benefits package including health cover and contributory pension</span></li><li style="margin-left: .25in;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Unrivalled opportunities to develop a successful career in the scientific industry</span></li><li style="margin-left: .25in;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Unsurpassed career development opportunities, with the ability to develop your management skills</span></li><li style="margin-left: .25in;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Ability to work with a variety of different clients on wide ranging projects</span></li><li style="margin-left: .25in;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Opportunity to work in a rapidly expanding and leading edge field</span></li></ul><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>Interested? Then apply today to join Covance by Labcorp and help us achieve our mission – to be the best company to work with and the best company to work for!!</strong></span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>Relocation may be available for this role</strong></span></p><h2>Education/Qualifications:</h2><ul><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">A science or chemistry related degree or equivalent experience</span></li></ul><h2>Experience:</h2><ul><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Proven experience of working in Bioanalysis LC-MS/MS within a CRO/pharmaceutical environment as a bioanalytical study manager/study director or equivalent</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Highly skilled in conducting research, data interpretation and writing reports</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Proven record of accomplishment of managing regulated bioanalytical preclinical and clinical studies</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Client facing experience is desirable</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Experience and knowledge of analytical instrumentation (LC/MS/MS) and its application in bioanalysis</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Highly skilled in performing scientific presentation and preparing scientific publications</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Knowledge of laboratory automation, scientific system software, LIMS, and Microsoft applications</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Effective oral and written communication skills along with great organisational skills</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Has worked within a GLP/GCP environment</span></li></ul>