Senior Medical Director / Medical Director - Head & Neck Oncology

<h2>Job Overview:</h2><p style="margin: 0px;"><span style="font-size: 10.0pt;">Reporting to the Executive Medical Director, the primary role of the <strong>Senior Medical Director / Medical Director</strong> will be to serve as a physician providing medical delivery services and subject matter and drug development expertise.  He/She will be expected to be a key contributor to the medical strategy and execution of clinical programs.  Furthermore, the Senior Medical Director / Medical Director will play a key role in people leadership/management, client relations, and business development representing Covance by Labcorp in proposals and industry meetings as needed.  This is a remote home-based role with travel (US and Global) as needed.</span></p><p style="margin: 0px;"><span style="font-size: 10.0pt;"> </span></p><p style="margin: 0px;"><span style="font-size: 10.0pt;">Responsibilities to include;</span></p><p style="margin: 0px;"><span style="font-size: 10.0pt;"> </span></p><p style="margin: 0px;"><span style="font-size: 10pt;"><strong><u>Client Relationship & Business Development Activities</u></strong></span></p><p style="margin: 0px;"><span style="font-size: 10.0pt;"> </span></p><ul><li style="margin-left: .5in;"><span style="font-size: 10.0pt;">Partnering with GCO to develop new and enhance existing client relationships where possible</span></li><li style="margin-left: .5in;"><span style="font-size: 10.0pt;">Provides leadership and presents medical/scientific capabilities to clients as a participant of a proposal team</span></li><li style="margin-left: .5in;"><span style="font-size: 10.0pt;">Leverage known and builds new relationships with investigators/sites to performs site/ investigator feasibility and to support optimal recruiting and conduct of trials</span></li><li style="margin-left: .5in;"><span style="font-size: 10.0pt;">Able to present or serve on panels to represent the company at conferences and scientific meetings.</span></li></ul><p style="margin: 0px;"><span style="font-size: 10.0pt;"> </span></p><p style="margin: 0px;"><span style="font-size: 10pt;"><strong><u>Therapeutic and Scientific Expertise</u></strong></span></p><p style="margin: 0px;"><span style="font-size: 10.0pt;"> </span></p><ul><li style="margin-left: .5in;"><span style="font-size: 10.0pt;">Responsible for medical and safety monitoring on assigned projects</span></li><li style="margin-left: .5in;"><span style="font-size: 10.0pt;">Develops training modules and materials, and provides training in disease states and protocol specific requirements</span></li><li style="margin-left: .5in;"><span style="font-size: 10.0pt;">Participates in training opportunities to advance knowledge of drug development and good clinical practice guidelines</span></li><li style="margin-left: .5in;"><span style="font-size: 10.0pt;">Serve as global lead project physician and provides clinical and medical expertise</span></li><li style="margin-left: .5in;"><span style="font-size: 10.0pt;">May serve as a program level physician across multiple studies for a given company</span></li><li style="margin-left: .5in;"><span style="font-size: 10.0pt;">Provides subject matter and drug development expertise to be a key contributor to the medical strategy and execution of the program for the client</span></li><li style="margin-left: .5in;"><span style="font-size: 10.0pt;">Performs medical data review and/or oversight of central medical data review- laboratory values, adverse events, coding dictionaries and data tables, listings and figures as needed, holistic and aggregated data review</span></li><li style="margin-left: .5in;"><span style="font-size: 10.0pt;">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: .5in;"><span style="font-size: 10.0pt;">Prepares materials for investigator meetings</span></li><li style="margin-left: .5in;"><span style="font-size: 10.0pt;">Actively participates in investigator meetings</span></li><li style="margin-left: .5in;"><span style="font-size: 10.0pt;">Provides medical/scientific expertise to project teams and to other Covance departments</span></li><li style="margin-left: .5in;"><span style="font-size: 10.0pt;">Interacts with inter-departmental and external consultants as appropriate</span></li><li style="margin-left: .5in;"><span style="font-size: 10.0pt;">Participates in feasibility discussions relating to specific project proposals</span></li><li style="margin-left: .5in;"><span style="font-size: 10.0pt;">Participates in project risk assessment activities</span></li><li style="margin-left: .5in;"><span style="font-size: 10.0pt;">Assists when needed with data safety monitoring board activities</span></li><li style="margin-left: .5in;"><span style="font-size: 10.0pt;">Contributes to the scientific strategic leadership for the Oncology programs</span></li></ul><h2>Education/Qualifications:</h2><p style="margin: 0px;"> </p><ul><li><span style="font-size: 10.0pt;">Doctor of Medicine </span></li><li><span style="font-size: 10.0pt;">BE/BC in Oncology and/or Hematology</span></li></ul><h2>Experience:</h2><ul><li><span style="font-size: 10.0pt;">Experience with medical monitoring of Oncology clinical trials</span></li><li><span style="font-size: 10.0pt;">Previous experience within the CRO or Pharmaceutical/Biotech industry</span></li><li><span style="font-size: 10.0pt;">History of trial work with focus in head / neck <span>squamous cell carcinomas</span></span></li></ul>