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Job #03534

About our client Our Client is a full service CRO based in Arizona. They offer Phase I – IV clinical trial abilities in multiple therapeutic areas. The company has strong financials, an experienced management team and a loyal customer base. They have developed an industry-wide reputation for a positive work environment and an aggressive training program that ensures employees are up to date on current trends and best practices. This is a strong opportunity for someone that wants to put their drive and initiative to work! Position Location Chief Medical Director Arizona Salary Highly competitive package, commensurate with experience Responsibilities 1) Acts as Principal Investigator/Sub-Investigator. 2) Reviews and evaluates protocols and Investigator Brochures and provides clinical and scientific support as needed. 3) In conjunction with the Chief Operations Officer, makes recommendations for scheduling, logistics and feasibility for proposed studies. 4) Acts as a consultant to clients in regard to scientific/medical aspects of clinical study designs. 5) Evaluates the performance of the medical staff. 6) Ensures medical coverage for clinical studies. 7) Establishes and maintains close affiliations with the medical community. 8) Ensures that the highest levels of client service are maintained. 9) Performs study physical examinations and reviews vital signs, medical histories, ECGs, and laboratory results to ensure that volunteers meet inclusion/exclusion criteria for the study. 10) Performs on-study and post-study examinations and reviews adverse events, vital signs, ECGs, and laboratory results to ensure that safety and well being of study participants is assured throughout the study. 11) Reviews relevant data for dose escalation and attends safety reviews with clients, as required. 12) Administers test articles to study participants or delegates this task to qualified staff when appropriate. 13) Informs clients, IRB, and upper management of significant study issues. 14) Assists CEO with client proposals and attend client meetings as needed. 15) Attends new client visits and promotes Phase I and IIa business as appropriate. 16) Ensures the Safety of the Study Participants and Conduct Staff. 17) Supervises and manages the safety team including paramedics and EMT, RN/ LPN or Physicians Assistant. Requirements 1) M. D. license and DEA license. 2) Minimum of 5 years experience post residency in a clinical setting. 3) Well versed in ICH-GCP principles. 4) Understanding of drug development and clinical research principles; previous clinical research experience preferred. 5) Strong planning and organizational capabilities to manage multiple projects. 6) Can work independently on multiple tasks and manage time effectively. 7) Problem solving where development of new solutions, methods and systems will result in a major impact on department's overall success. 8) Develop/implement/own recommendations and see projects through to completion. 9) Analyze current methods and procedures, recommend and implement improvements. 10) Ability to communicate effectively by telephone, in group meetings, and discussions.