Medical Dir - MD

Job Overview:Labcorp Drug Development is seeking a Medical Director to join our Clinical Pharmacology team based in Madison, WI. 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. Key responsibilities and duties to include;Company FocusContributes to the development of Company policies involving medical, safety, and therapeuticsParticipates in process improvement activities across CompanyClient Relationship & Business Development ActivitiesPartnering with GCO to develop new and enhance existing client relationships where possibleProvides medical/scientific capabilities to clients as a participant of a proposal teamPerforms site/investigator feasibility, builds relationships with investigators to support optimal recruiting and conduct of trialsManagerial and LeadershipSupports and participates in the recruitment process for department positionProvides leadership to junior staff within clinical pharmacologyParticipates and leads initiatives that serves the physicians within clinical pharmacologyTherapeutic and Scientific ExpertiseDevelops training modules and materials, and provides training in disease states and protocol specific requirements across the CompanyParticipates in training opportunities to advance knowledge of drug development and good clinical practice guidelinesServes as global lead project physician Performs medical data review - reviews laboratory values, adverse events, coding dictionaries and data tables, listings and figures as neededDevelops, reviews and revises protocol, case report forms, training material, project specific tools, analysis plans design, clinical trial reports and new drug applicationsPrepares materials for investigator meetings and site initiation visitsActively participates in investigator meetings and site initiation visitsProvides medical/scientific expertise to project teamsResponsible for medical and safety monitoring on assigned projectsInteracts with interdepartmental and external consultants as appropriateParticipates in feasibility discussions relating to specific project proposalsParticipates in project risk assessment activitiesAssists when needed with data safety monitoring board activitiesProvides clinical and medical expertise to other departmentsEducation/Qualifications:MD Degree with postgraduate clinical trainingRelevant sub-specialty fellowship training preferredBoard Certification history preferredExperience:3+ years of experience with substantial knowledge of drug development and extensive clinical research experience within the pharmaceutical/CRO industry in a specific therapeutic areaPhase 1 background preferred