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Medical Director, Respiratory Diseases

Laboratory Corporation of America Holdings (Covance)

Munich, Germany

<h2>Job Overview:</h2><p style="margin: 0px;">Medical Director opportunity - Respiratory Diseases. This position is to conduct medical monitoring  within global clincial trials, managed within labcorp Drug Develoment. In particular, you will be the medical expert for Respiratory clinical studies.</p><p style="margin: 0px;"> </p><p style="margin: 0px;">Flexible locations can be considered within the EMEA region. We are looking for a medical professional (MD) with previous experience in preforming medical monitoring activities within Respiratory Clinical Trials.</p><p style="margin: 0px;"> </p><p style="margin: 0px;">Associate Medical Director level may be considered, depending on experience level.</p><p style="margin: 0px;"> </p><p style="margin: 0px;">Main responsibilities to include:</p><p style="margin: 0px;"> </p><ul><li><span style="color: black; font-family: 'Arial',sans-serif; font-size: 10pt;">Serves as Lead Project Physician or as Program Level Physician in his/ her area of expertise</span></li><li><span style="color: black; font-family: 'Arial',sans-serif; font-size: 10pt;">Develops training modules and materials as required, and provides training in disease areas and protocol specific requirements across the company</span></li><li><span style="color: black; font-family: 'Arial',sans-serif; font-size: 10pt;">Oversight and review of escalated issues/gaps and proposals for process improvement and initiatives </span></li><li><span style="color: black; font-family: 'Arial',sans-serif; font-size: 10pt;">Performs medical data review; reviews laboratory values, adverse events, coding dictionaries and data tables, listings and figures as needed</span></li><li><span style="color: black; font-family: 'Arial',sans-serif; font-size: 10pt;">Provides input, review and revision of protocols, case report forms, training materials, project specific tools, analysis plans design, clinical trial reports and new drug applications</span></li><li><span style="color: black; font-family: 'Arial',sans-serif; font-size: 10pt;">Prepares materials for investigator meetings</span></li><li><span style="color: black; font-family: 'Arial',sans-serif; font-size: 10pt;">Actively participates in investigator meetings</span></li><li><span style="color: black; font-family: 'Arial',sans-serif; font-size: 10pt;">Provides medical/scientific expertise to project teams</span></li><li><span style="color: black; font-family: 'Arial',sans-serif; font-size: 10pt;">Responsible for medical and safety monitoring on assigned projects</span></li><li><span style="color: black; font-family: 'Arial',sans-serif; font-size: 10pt;">Interacts with inter-departmental and external consultants as appropriate</span></li><li><span style="color: black; font-family: 'Arial',sans-serif; font-size: 10pt;">Participates in feasibility discussions relating to specific project proposals</span></li><li><span style="color: black; font-family: 'Arial',sans-serif; font-size: 10pt;">Participates in project risk assessment activities</span></li><li><span style="color: black; font-family: 'Arial',sans-serif; font-size: 10pt;">Provides out of hours medical cover as required</span></li><li><span style="color: black; font-family: 'Arial',sans-serif; font-size: 10pt;">Assists when needed with data safety monitoring board activities</span></li><li><span style="color: black; font-family: 'Arial',sans-serif; font-size: 10pt;">Provides Clinical and medical expertise to other Covance departments</span></li><li><span style="color: black; font-family: 'Arial',sans-serif; font-size: 10pt;">Provides evaluation and oversight of medical data review performed by central medical data reviewers</span></li><li><span style="color: black; font-family: 'Arial',sans-serif; font-size: 10pt;">Reviews and/or assists with medical monitoring scope of work/hours and budget discussions as required for new proposals and assigned studies</span></li><li><span style="color: black; font-family: 'Arial',sans-serif; font-size: 10pt;">Provides oversight of Project and Medical Management to ensure timelines and quality of medical deliverables and assigns physician resources as required</span></li><li><span style="color: black; font-family: 'Arial',sans-serif; font-size: 10pt;">Maintains subject matter expertise through ongoing continuing medical education (CME) or clinical work as well as attendance at relevant conference/meetings</span></li><li><span style="color: black; font-family: 'Arial',sans-serif; font-size: 10pt;">Provides subject matter and drug development expertise and is a key contributor to the medical strategy and execution of the study/program for the client</span></li></ul><p style="margin: 0px;"> </p><p style="margin: 0px;"> </p><p style="margin: 0px;"> </p><p style="margin: 0px;"> </p><h2>Education/Qualifications:</h2><p style="margin: 0px;"><span style="font-family: arial,helvetica,sans-serif; font-size: 10pt;">Medical Doctor trained in Internal Medicine with significant experience in Respiratory Medicine.</span></p><p style="margin: 0px;"><span style="font-family: arial,helvetica,sans-serif; font-size: 10pt;">Board certification in this area would be an advantage.</span></p><h2>Experience:</h2><p style="margin: 0px;"><span style="font-family: arial,helvetica,sans-serif; font-size: 10pt;"><span style="text-decoration: underline;">Mandatory:</span> Experience in Respiratory Diseases</span></p><p style="margin: 0px;"><span style="font-family: arial,helvetica,sans-serif; font-size: 10pt;"><span style="text-decoration: underline;">Optional:</span> Experience in other internal medicine sub-specialties would be desirable</span></p>

Job posted: 2021-08-12

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