(Snr) Medical Dir - Oncology

<h2>Job Overview:</h2><p style="margin: 0px;"><strong><span style="font-size: 11pt;">Essential Job Duties: </span></strong></p><p style="margin: 0px;"><strong><span style="font-size: 11pt;"> </span></strong></p><p style="margin: 0px;"><strong><u><span style="font-size: 11pt;">Company Focus</span></u></strong></p><p style="margin: 0px;"><span style="font-size: 11pt;"> </span></p><ul><li style="margin-left: 36pt;"><span style="font-size: 11pt;">Contributes to the development of Company policies involving medical, safety and therapeutics </span></li><li style="margin-left: 36pt;"><span style="font-size: 11pt;">Participates in process improvement activities across Company </span></li><li style="margin-left: 36pt;"><span style="font-size: 11pt;">Performs other duties as assigned</span></li></ul><p style="margin: 0px;"><span style="font-size: 11pt;"> </span></p><p style="margin: 0px;"><strong><u><span style="font-size: 11pt;">Client Relationship & Business Development Activities</span></u></strong></p><p style="margin: 0px;"><strong><u><span style="font-size: 11pt;"> </span></u></strong></p><ul><li style="margin-left: 36pt;"><span style="font-size: 11pt;">Partnering with GCO to develop new and enhance existing client relationships where possible</span></li><li style="margin-left: 36pt;"><span style="font-size: 11pt;">Presents medical/scientific capabilities to clients as a participant of a proposal team</span></li><li style="margin-left: 36pt;"><span style="font-size: 11pt;">Performs site/investigator feasibility, builds relationships with investigators to support optimal recruiting and conduct of trials  </span></li></ul><p style="margin: 0px;"><span style="font-size: 11pt;"> </span></p><p style="margin: 0px;"><strong><u><span style="font-size: 11pt;">Managerial</span></u></strong></p><p style="margin: 0px;"><span style="font-size: 11pt;"> </span></p><ul><li style="margin-left: 36pt;"><span style="font-size: 11pt;">Supports and participates in the recruitment process for department positions</span></li></ul><p style="margin: 0px;"><span style="font-size: 11pt;"> </span></p><p style="margin: 0px;"><strong><u><span style="font-size: 11pt;">Leadership</span></u></strong></p><p style="margin: 0px;"><span style="font-size: 11pt;"> </span></p><ul><li style="margin-left: 36pt;"><span style="font-size: 11pt;">Provides leadership to junior staff within the therapeutic area</span></li><li style="margin-left: 36pt;"><span style="font-size: 11pt;">Participates and leads initiatives that serves the physicians within the TA</span></li></ul><p style="margin: 0px;"><span style="font-size: 11pt;"> </span></p><p style="margin: 0px;"><strong><u><span style="font-size: 11pt;">Therapeutic and Scientific Expertise</span></u></strong></p><p style="margin: 0px;"><span style="font-size: 11pt;"> </span></p><ul><li style="margin-left: 36pt;"><span style="font-size: 11pt;">Develops training modules and materials, and provides training in disease states and protocol specific requirements across the Company</span></li><li style="margin-left: 36pt;"><span style="font-size: 11pt;">Participates in training opportunities to advance knowledge of drug development and good clinical practice guidelines</span></li><li style="margin-left: 36pt;"><span style="font-size: 11pt;">Serves as global lead project physician</span></li><li style="margin-left: 36pt;"><span style="font-size: 11pt;">Performs medical data review - Reviews laboratory values, adverse events, coding dictionaries and data tables, listings and figures as needed</span></li><li style="margin-left: 36pt;"><span style="font-size: 11pt;">Develops, reviews and revises protocols, case report forms, training materials, project specific tools, analysis plans design, clinical trial reports and new drug applications</span></li><li style="margin-left: 36pt;"><span style="font-size: 11pt;">Prepares materials for investigator meetings</span></li><li style="margin-left: 36pt;"><span style="font-size: 11pt;">Actively participates in investigator meetings</span></li><li style="margin-left: 36pt;"><span style="font-size: 11pt;">Provides medical/scientific expertise to project teams</span></li><li style="margin-left: 36pt;"><span style="font-size: 11pt;">Responsible for medical and safety monitoring on assigned projects</span></li><li style="margin-left: 36pt;"><span style="font-size: 11pt;">Interacts with inter-departmental and external consultants as appropriate</span></li><li style="margin-left: 36pt;"><span style="font-size: 11pt;">Participates in feasibility discussions relating to specific project proposals</span></li><li style="margin-left: 36pt;"><span style="font-size: 11pt;">Participates in project risk assessment activities</span></li><li style="margin-left: 36pt;"><span style="font-size: 11pt;">Assists when needed with data safety monitoring board activities</span></li><li style="margin-left: 36pt;"><span style="font-size: 11pt;">Provides clinical and medical expertise to other Covance departments</span></li></ul><h2>Education/Qualifications:</h2><h2><u>Minimum Required</u></h2><p style="margin: 0px;"> </p><ul><li>MD Degree</li></ul><p style="margin: 0px;"> </p><p style="margin: 0px;"><strong><u>Preferred</u></strong></p><p style="margin: 0px;"><strong><u> </u></strong></p><ul><li style="margin-left: 36.0pt;"><span style="font-size: 11.0pt;">Relevant sub specialty fellowship training and history of board certification</span></li></ul><h2>Experience:</h2><ul><li style="margin-left: 54.0pt;"><span style="font-size: 11.0pt;">At least 3-5 years’ experience with substantial knowledge of drug development and extensive clinical research experience within the pharmaceutical/CRO industry in a specific therapeutic area</span></li></ul>