Director Clinical Operations

<h2>Job Overview:</h2><p style="margin: 0px;"><span>Do you want a career that makes an impact on patient lives?  You can find it here at Labcorp Drug Development. We have a great opportunity for a Director Clinical Operations to join our team in Sweden or Denmark ( remote working). Our work in developing new pharmaceutical solutions has an incredible impact on millions of lives worldwide.  Be a part of this life-saving work.</span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span><strong>In this role, the Study Director will:</strong></span></p><p style="margin: 0px;"> </p><ul><li>Talent Management: Selection, Onboarding, Training & Retention</li><li>Budget and Fiances </li><li>accountable and responsible for execution of the country and/or regional quality plans and delivery on country quality metrics and quality delivery</li><li><p style="margin: 0px;">Coach staff to own effective investigator relations and investigator oversight at the local and/or regional level</p></li><li><p style="margin: 0px;">Liaise with management at other locations and Leadership to identify and implement opportunities for standardisation of process and increased efficiency within and between departments</p></li><li>Drive department resourcing strategy within designated area of responsibility including ensuring the right talent are assigned to the right projects at the right time; ensure that the talent is fully utilised</li><li>line management ( Denmark and Sweden) </li></ul><p style="margin: 0px;"> </p><h2>Education/Qualifications:</h2><p style="margin: 0px;"> </p><ul><li>Masters or other advanced degree from an appropriately accredited institution</li><li>University/college degree – life sciences preferred </li><li>Supervisory experience in a health care or clinical research setting and relevant clinical research experience in a pharmaceutical company/CRO</li></ul><h2>Experience:</h2><p style="margin: 0px;"> </p><ul><li>Relevant clinical research experience in a pharmaceutical company or CRO</li><li>Individual is proficient with on-site monitoring activities (including pre-study, initiation, routine monitoring and closeout visits)</li><li>supervisory experience, including f managing managers, in a health care or clinical research setting </li><li>Thorough knowledge of drug development process</li><li>Thorough knowledge of relevant SOPs, ICH, and GCP guidelines</li><li>Demonstrated ability to lead by example and to encourage team members to seek solutions</li><li>Proven interpersonal skills</li><li>Excellent planning and organisational skills</li><li>Demonstrated ability to successfully manage multiple competing priorities</li><li>Excellent oral, written and presentation skills</li><li>fluent in English and local language </li></ul><p style="margin: 0px;"> </p>