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Sr. Medical Director / Medical Director – Respiratory / Pulmonary

Covance

This is a Contract position in Chicago, IL posted January 12, 2021.

Job Description
Job Overview: Reporting to the Executive Medical Director, the primary role of the incumbent will be to provide subject matter and drug development expertise in support of Respiratory/Pulmonary drug development trials. He/She will be expected to be a key contributor to the medical strategy and execution of clinical programs. Furthermore, the Medical Director or Sr. Medical Director will play a key role in client relations, business development representing Covance in proposals and industry meetings, and potentially people leadership/management as needed. This is a remote home-based role supporting US trials. Client Relationship & Business Development Activities * Partnering with GCO to develop new and enhance existing client relationships where possible * Provides leadership and presents medical/scientific capabilities to clients as a participant of a proposal team * Leverage known and builds new relationships with investigators/sites to performs site/ investigator feasibility and to support optimal recruiting and conduct of trials * Able to present or serve on panels to represent the company at conferences and scientific meetings. Therapeutic and Scientific Expertise * Responsible for medical and safety monitoring on assigned projects * Develops training modules and materials, and provides training in disease states and protocol specific requirements * Participates in training opportunities to advance knowledge of drug development and good clinical practice guidelines * Serve as global lead project physician and provides clinical and medical expertise * May serve as a program level physician across multiple studies for a given company * Provides subject matter and drug development expertise to be a key contributor to the medical strategy and execution of the program for the client * 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 * Develops, reviews and revises protocols, case report forms, training materials, project specific tools, analysis plans design, clinical trial reports and new drug applications * Prepares materials for investigator meetings * Actively participates in investigator meetings * Provides medical/scientific expertise to project teams and to other Covance departments * Interacts with inter-departmental and external consultants as appropriate * Participates in feasibility discussions relating to specific project proposals * Participates in project risk assessment activities * Assists when needed with data safety monitoring board activities * Contributes to the scientific strategic leadership for clinical programs. Education/Qualifications: * MD degree * Fellowship trained in Pulmonary and/or Respiratory Disease * History of Board Certification in Pulmonary and/or Respiratory Disease is highly preferred * Excellent communication and interpersonal skills Experience: * 5+ years of medical monitoring experience in CRO or Pharma/Biotech * Experience with Pulmonary/Respiratory trials; COPD, Asthma * Experience supporting Phase II- IV clinical trials * Previous experience in clinical patient care preferred

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