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Associate Line Manager - sponsor dedicated

Laboratory Corporation of America Holdings (Covance)

Czech Republic

<h2>Job Overview:</h2><p style="margin: 0px;">As an Associate Manager, Clinical Operations, you would be responsible for the supervision of <span>of assigned direct reports within Clinical Operations, FSP and/or Global Site Services as well as the Sponsor interaction.</span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span>Key Responsiblities:</span></p><ul><li>Responsible for detailed performance review and management of assigned direct reports including: Annual Performance Management and Development (PMD), Individual Development Plan (IDP), Line of Sight Goals and “Shoves & Tugs”</li><li>Responsible for appropriate management and resolution of performance issues</li><li>Develop and measure performance indicators for assigned staff</li><li>Identify individual training needs and assist with the coordination and conduct of training and development efforts, regionally</li><li>Coordinate, conduct, report and follow-up on Quality Control Visits (CQC)</li><li>Effectively communicate management strategies, policies and procedures in conjunction with leadership teams</li><li>Develop and maintain effective relationships with management team to manage assigned staff in a matrix environment</li><li>Maintain good working relationships with internal and external clients to ensure opportunity for acquiring additional new business</li></ul><h2>Education/Qualifications:</h2><ul><li>University/college degree – life sciences preferred or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)</li><li>In lieu of this required educational background the following relevant work history may be considered:</li><li>Proven supervisory experience in a health care or clinical research setting and</li><li>Relevant clinical research experience in a pharmaceutical company/CRO</li></ul><h2>Experience:</h2><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>Proven relevant clinical research experience in a pharmaceutical company/CRO</li><li>Thorough knowledge of drug development process</li><li>Thorough knowledge of relevant SOPs, ICH, and GCP guidelines</li><li>Relevant supervisory experience</li><li>Minimum of 3 years as a Line Manager or Project Manager required</li><li>Demonstrated ability to lead by example and to encourage team members to seek solutions</li><li>Proven interpersonal skills</li><li>Demonstrated ability to successfully participate as a member of a project team</li><li>Demonstrated ability to successfully manage multiple competing priorities</li><li>Advanced planning and organizational skills</li><li>Advanced oral, written and presentation skills</li></ul>

Job posted: 2021-11-03

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