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Medical Director - Phase I

Laboratory Corporation of America Holdings (Covance)

Harrogate, United Kingdom

<h2>Job Overview:</h2><p style="margin: 0px;"><span style="font-size: 10pt;">Labcorp Drug Development is seeking a Medical Director with strong Phase I study experience to join our team. Reporting to the Executive Medical Director, Clinical Pharmacology, the incumbent will be responsible for providing medical direction for the conduct of early clinical trials. Additionally, the Medical Director will be responsible for supporting the development activities of proposed and ongoing projects in their area of expertise, as well as medical monitoring for assigned clinical studies. </span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-size: 10pt;">This is a remote role and can be based in the EU or UK.</span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-size: 10pt;">Key responsibilities and duties to include;</span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-size: 10pt;"><u>Company Focus</u></span></p><ul><li style="margin-left: .25in;"><span style="font-size: 10pt;">Contributes to the development of Company policies involving medical, safety, and therapeutics</span></li><li style="margin-left: .25in;"><span style="font-size: 10pt;">Participates in process improvement activities across Company</span></li></ul><p style="margin: 0px;"><span style="font-size: 10pt;"><u>Client Relationship & Business Development Activities</u></span></p><ul><li style="margin-left: .25in;"><span style="font-size: 10pt;">Partnering with GCO to develop new and enhance existing client relationships where possible</span></li><li style="margin-left: .25in;"><span style="font-size: 10pt;">Provides medical/scientific capabilities to clients as a participant of a proposal team</span></li><li style="margin-left: .25in;"><span style="font-size: 10pt;">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: 10pt;"><u>Managerial and Leadership</u></span></p><ul><li style="margin-left: .25in;"><span style="font-size: 10pt;">Supports and participates in the recruitment process for department position</span></li><li style="margin-left: .25in;"><span style="font-size: 10pt;">Provides leadership to junior staff within clinical pharmacology</span></li><li style="margin-left: .25in;"><span style="font-size: 10pt;">Participates and leads initiatives that serves the physicians within clinical pharmacology</span></li></ul><p style="margin: 0px;"><span style="font-size: 10pt;"><u>Therapeutic and Scientific Expertise</u></span></p><ul><li style="margin-left: .25in;"><span style="font-size: 10pt;">Develops training modules and materials, and provides training in disease states and protocol specific requirements across the Company</span></li><li style="margin-left: .25in;"><span style="font-size: 10pt;">Participates in training opportunities to advance knowledge of drug development and good clinical practice guidelines</span></li><li style="margin-left: .25in;"><span style="font-size: 10pt;">Serves as global lead project physician </span></li><li style="margin-left: .25in;"><span style="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 style="margin-left: .25in;"><span style="font-size: 10pt;">Develops, reviews and revises protocol, case report forms, training material, project specific tools, analysis plans design, clinical trial reports and new drug applications</span></li><li style="margin-left: .25in;"><span style="font-size: 10pt;">Prepares materials for investigator meetings and site initiation visits</span></li><li style="margin-left: .25in;"><span style="font-size: 10pt;">Actively participates in investigator meetings and site initiation visits</span></li><li style="margin-left: .25in;"><span style="font-size: 10pt;">Provides medical/scientific expertise to project teams</span></li><li style="margin-left: .25in;"><span style="font-size: 10pt;">Responsible for medical and safety monitoring on assigned projects</span></li><li style="margin-left: .25in;"><span style="font-size: 10pt;">Interacts with interdepartmental and external consultants as appropriate</span></li><li style="margin-left: .25in;"><span style="font-size: 10pt;">Participates in feasibility discussions relating to specific project proposals</span></li><li style="margin-left: .25in;"><span style="font-size: 10pt;">Participates in project risk assessment activities</span></li><li style="margin-left: .25in;"><span style="font-size: 10pt;">Assists when needed with data safety monitoring board activities</span></li><li style="margin-left: .25in;"><span style="font-size: 10pt;">Provides clinical and medical expertise to other departments</span></li></ul><h2>Education/Qualifications:</h2><ul><li><span style="font-size: 10pt;">MD Degree with post graduate clinical training</span></li><li><span style="font-size: 10pt;">Phase 1 experience as PI or Medical Monitor</span></li><li><span style="font-size: 10pt;">Relevant sub specialty fellowship training and history of board certification highly preferred</span></li></ul><h2>Experience:</h2><ul><li><span style="font-size: 10pt;">3+ years of experience with substantial knowledge of drug development and extensive clinical research experience within the pharmaceutical/CRO industry in a specific therapeutic area</span></li><li><span style="font-size: 10pt;">Equivalent academic experience can be substituted</span></li></ul>

Job posted: 2021-12-03

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