Lead Clinical Data Manager - Early Phase

<h2>Job Overview:</h2><ul><li><span style="font-size: 10.0pt;">You will be permanently employed by Labcorp Drug Development working in our Clinical Pharmacology Services (CPS) division working across multiple Sponsors and multiple therapeutic areas in Phases I to IIa.</span></li><li><span style="font-size: 10.0pt;">Office based or home based anywhere in Europe or South Africa.</span></li><li><span style="font-size: 10.0pt;">You must have previous experience of working in a clinical data management lead role within clinical research.</span></li><li><span style="font-size: 10.0pt;">Candidates must be fluent in English language (both verbal and written).</span></li></ul><p style="margin: 0px;"><span style="font-size: 10.0pt;">Join our growing team and discover your extraordinary potential by working as a Labcorp Clinical Data Manager within our  Clinical Pharmacology Services department.  The CPS department works across multiple therapeutic areas in Phases I to IIa with multiple Sponsors.  The position offers a strong support network, flexible working solutions and the opportunity to progress your career.  If you are looking to strengthen your expertise within a varied and dynamic environment, then this is a fantastic opportunity.  This is a permanent, full-time office or home-based role anywhere within Europe or South Africa.</span></p><h2>Education/Qualifications:</h2><ul><li><span style="font-size: 10.0pt;">University/college degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology).</span></li><li><span style="font-size: 10.0pt;">Knowledge of drug development process.</span></li><li><span style="font-size: 10.0pt;">Knowledge of effective clinical data management practices.</span></li><li><span style="font-size: 10.0pt;">Fluent in English, both written and verbal.</span></li><li><span style="font-size: 10.0pt;">In lieu of above requirement, approximately six years’ experience in related field (e.g. pharmaceutical, laboratory, data analysis).</span></li></ul><h2>Experience:</h2><ul><li><span style="font-size: 10.0pt;">Proven experience in handling customer negotiations and experience with managing Scope of Work and budgets.</span></li><li><span style="font-size: 10.0pt;">Thorough knowledge of clinical trial process, DM, clinical operations, biometrics, and system applications to support operations.</span></li><li><span style="font-size: 10.0pt;">Proven ability to lead by example on project strategies and achievement of department goals, objectives and initiatives and to encourage team members to seek solutions.</span></li><li><span style="font-size: 10.0pt;">Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical/biotechnological companies.</span></li><li><span style="font-size: 10.0pt;">Time management skill and ability to adhere to project productivity metrics and timelines.</span></li><li><span style="font-size: 10.0pt;">Ability to work in a team environment and collaborate with peers.</span></li><li><span style="font-size: 10.0pt;">Good organizational ability, communication and interpersonal skills.</span></li><li><span style="font-size: 10.0pt;">Team working skills and good collaborator skills.</span></li><li><span style="font-size: 10.0pt;">Constructive problem solving attitude while deadline focused with time demands, incomplete information or unexpected events.</span></li><li><span style="font-size: 10.0pt;">Knowledge of medical terminology.</span></li><li><span style="font-size: 10.0pt;">Knowledge of science or a scientific background is preferred.</span></li><li><span style="font-size: 10pt;">Good oral and written communication skills.</span></li></ul><p style="margin: 0cm; margin-bottom: .0001pt;"><span style="font-size: 10pt;"><strong><span style="font-family: Calibri, sans-serif; color: black;">MORE INFORMATION AVAILABLE ON REQUEST</span></strong></span></p><p style="margin: 0cm; margin-bottom: .0001pt;"> </p><p style="margin: 0cm; margin-bottom: .0001pt;"><span style="font-size: 10pt;"><span style="font-family: Calibri, sans-serif; color: black;">For a confidential discussion about this opportunity, please phone Antony McAteer on </span><span style="font-family: Calibri, sans-serif; color: black;">+44 (0) 7800 913 717</span><span style="font-family: Calibri, sans-serif; color: black;">.  To apply, please click on the APPLY button.  </span></span></p><p style="margin: 0cm; margin-bottom: .0001pt;"><span style="font-size: 10.0pt; font-family: 'Calibri',sans-serif; color: black;"> </span></p><p style="margin: 0px;"><span style="font-size: 10pt;"><strong><u>Keywords:</u></strong></span></p><p style="margin: 0px;"><span style="font-size: 10.0pt;">Labcorp Drug Development, Covance by Labcorp, Covance, Chiltern, Phase I, Phase IIa, Phase II, CRO, Contract Research Organisation, Contract Research Organization, pharma, pharmaceutical, clinical data manager, clinical data management, Clinical Data Management, Clinical Data Management, home based, pharma, home-based, flexible working, flexible location, field based, home based EU Anywhere, anywhere in Europe, field-based, United Kingdom, UK, Great Britain, England, Maidenhead, Reading, Berkshire, Birmingham, Cambridge, Sheffield, Manchester, Alderley Edge, Scotland, Edinburgh, Wales, Swansea, Northern Ireland, Austria, Belgium, Bulgaria, Czech Republic, France, Paris, Germany, Greece, Hungary, Ireland, Italy, Lithuania, Netherlands, Leiden, Poland, Portugal, Romania, Russia, Slovakia,  Bloemfontein, Centurion, South Africa, Madrid, Barcelona, Spain, Ukraine, <strong><span style="font-family: 'Calibri',sans-serif; color: black; border: none windowtext 1.0pt; padding: 0cm;">#LI-Remote, </span></strong><span style="color: black; border: none windowtext 1.0pt; padding: 0cm;">Remote, EMEA</span></span></p>