LOCAL CLINICAL PROJECT MANAGER, UK, CLIENT DEDICATED

<h2>Job Overview:</h2><p style="margin: 0px;"><span style="font-size: 11.0pt; font-family: 'Arial',sans-serif; color: black;">In the UK, our <strong>sponsor dedicated</strong> team continues its expansion, and we have new opportunities for several <strong>Local Clinical Project Managers</strong></span></p><p style="margin: 0px;"><span style="font-size: 11.0pt; font-family: 'Arial',sans-serif; color: black;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><strong><span style="font-size: 11.0pt; color: windowtext;">THE LOCAL CLINICAL PROJECT MANAGER / PM JOB</span></strong></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: #0a0a0a;"> </span></p><ul><li><span style="font-size: 11.0pt; color: windowtext;">You will work </span><span style="font-size: 11.0pt; color: windowtext;">sponsor dedicated </span><span style="font-size: 11.0pt; color: windowtext;">for a prestigious Top 5 global Pharmaceutical company.</span></li><li><span style="font-size: 11.0pt; color: windowtext;">We need you to bring experience in one/ various of the following therapeutic areas: </span><strong><span style="font-size: 11.0pt; color: windowtext;">Virology</span><span style="font-size: 11.0pt; color: windowtext;">, </span><span style="font-size: 11.0pt; color: windowtext;">Infectious Diseases</span><span style="font-size: 11.0pt; color: windowtext;">, </span><span style="font-size: 11.0pt; color: windowtext;">Oncology</span></strong></li><li><span style="font-size: 11.0pt; color: windowtext;">This job is located in the UK, 100% home based</span><span style="font-size: 11.0pt; color: windowtext;">. </span></li></ul><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;">These jobs are perfect to gain a combined and rich experience within the CRO and Sponsor environments. It would suit existing:</span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><ul><li><span style="font-size: 11.0pt; color: windowtext;">CRO-based Clinical Team Leaders or </span><span style="font-size: 11.0pt; color: black;">Project Managers </span><span style="font-size: 11.0pt; color: windowtext;">looking for a closer partnership with a Sponsor, or </span></li><li><span style="font-size: 11.0pt; color: windowtext;">Biopharmaceutical based Local Study Managers, Clinical Trial Managers or Project Managers looking to have experience within a Global CRO.</span></li></ul><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;">Under the oversight of the Country Therapeutic Area Director, you will be responsible at country level for the performance and execution of your assigned protocols from feasibility to close out.</span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;">This position has a significant impact on how the UK can deliver country-specific trial commitments and objectives. Unlike other roles with a similar job title, you will not be involved with Submissions or Budget management, rather your time will be dedicated to the clinical side:</span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><ul><li><span style="font-size: 11.0pt; color: windowtext;">The successful execution, enrollment and quality of your assigned clinical trials</span></li><li><span style="font-size: 11.0pt; color: windowtext;">Active participation in Feasibilities </span></li><li><span style="font-size: 11.0pt; color: windowtext;">Ensure timelines and key milestones are met in assigned clinical trials</span></li><li><span style="font-size: 11.0pt; color: windowtext;">Quality and compliance, engaged with quality control visits, Monitoring Visits Report review, escalating performance issues.</span></li><li><span style="font-size: 11.0pt; color: windowtext;">Functionally overseeing a team of CRAs & CTAs and guide them to high performance. </span></li></ul><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><strong><span style="font-size: 11.0pt; color: windowtext;">WHAT MAKES THESE JOBS SPECIAL</span></strong></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><ul><li><span style="font-size: 11.0pt; color: windowtext;">You will be dedicated to a prestigious TOP 5 Global Pharmaceutical company, with a unique opportunity to be part of the full drug development cycle, seeing a product from launch through closure.</span></li></ul><ul><li><span style="font-size: 11.0pt; color: windowtext;">This is a pure customer-facing role, allowing you to build high-level business relationships, especially representing the sponsor to investigators and managing the relationship with vendors and external partners.</span></li></ul><ul><li><span style="font-size: 11.0pt; color: windowtext;">You will be exposed to a rich interaction with internal client partners such as Unit Heads, Pharmacovigilance, Regulatory, Medical Affairs, etc. </span></li></ul><ul><li><span style="font-size: 11.0pt; color: windowtext;">You coordinate a wide range of activities across different local country roles ensuring a strong collaboration.</span></li></ul><ul><li><span style="font-size: 11.0pt; color: windowtext;">Covance has a long term relationship with the client. We have a well-organized structure, robust processes in place and unambiguous communication channels. </span></li></ul><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><strong><span style="font-size: 11.0pt; color: windowtext;">OTHER INFORMATION</span></strong></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: #0a0a0a;">This role is a full time & permanent position to be employed through Covance. For more information please contact Andy Smith on 07775 848 250</span><span style="font-size: 9.0pt; color: #252525;">  </span><span style="font-size: 11.0pt; color: #0a0a0a;">or mail andy.smith@covance.com</span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><strong><span style="font-size: 11.0pt; color: #0a0a0a;">COVANCE ARE PRACTICING SOCIAL DISTANCING WITH VIDEO INTERVIEWS </span></strong></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: #0a0a0a;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: #0a0a0a;">All your interviews with us will be conducted via phone or using WebEx video. To help you prepare, check out this brief guide for best practices and WebEx guidance:</span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><a href="https://www.labcorp.com/labcorp-enterprise-video-interviewing-guide" target="_blank" rel="noopener"><span style="font-size: 11.0pt;">https://www.labcorp.com/labcorp-enterprise-video-interviewing-guide</span></a></p><h2>Education/Qualifications:</h2><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: windowtext;">BSc or Master´s degree with strong emphasis in science and/or biology </span></p><h2>Experience:</h2><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: #0a0a0a;">This is a high profile job for Covance, this is why we can only consider candidates with:</span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 11.0pt; color: #0a0a0a;"> </span></p><ul><li><span style="font-size: 11.0pt; color: windowtext;">Significant scientific and clinical research experience in a sponsor/CRO: we need you to have developed your career as a CRA and then having some experience coordinating teams & projects in a matrix organization  </span></li><li><span style="font-size: 11.0pt; color: #0a0a0a;"> </span><span style="font-size: 11.0pt; color: windowtext;">A strong understanding of clinical trial planning, management and metrics is essential, as well as the ability to focus on multiple deliverables and protocols simultaneously. </span></li><li><span style="font-size: 11.0pt; color: windowtext;"> </span><span style="font-size: 11.0pt; color: windowtext;">Communication, educational and empathic skills to effectively build and maintain professional relationships with investigators and other external stakeholders</span></li><li><strong><span style="font-size: 11.0pt; color: windowtext;"> </span></strong><span style="font-size: 11.0pt; color: windowtext;">Proven ability to collaborate and lead high performing cross-functional teams also in a virtual environment.</span></li></ul>