Global Channel Management, Inc.
Clinical Trials Manager
Global Channel Management, Inc., Fort Lee, New Jersey, us, 07024
Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs while requiring the best talent for the job.Qualifications
The Clinical Trial Manager needs a Bachelor's degree and a minimum of 3 years experience in the healthcare or clinical trial industry, or the equivalent combination of education and experience.The Clinical Trial Manager requires:Extensive knowledge of clinical development principles, theories, and concepts, and a high degree of comprehension of pharmaceutical industry practices, standards, and GCP's.Thorough working knowledge of the clinical trial lifecycle from protocol development and feasibility through study closeout and reporting.Ability to manage complex, multiple studies simultaneously, some of which may be of a global nature.Manages/oversees the conduct and execution of assigned clinical trials and associated activities in accordance with Good Clinical Practices (GCP) and relevant standards.Assists with the review and determination of appropriate site and vendor selection and ensures all vendors meet predetermined program milestones.
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The Clinical Trial Manager needs a Bachelor's degree and a minimum of 3 years experience in the healthcare or clinical trial industry, or the equivalent combination of education and experience.The Clinical Trial Manager requires:Extensive knowledge of clinical development principles, theories, and concepts, and a high degree of comprehension of pharmaceutical industry practices, standards, and GCP's.Thorough working knowledge of the clinical trial lifecycle from protocol development and feasibility through study closeout and reporting.Ability to manage complex, multiple studies simultaneously, some of which may be of a global nature.Manages/oversees the conduct and execution of assigned clinical trials and associated activities in accordance with Good Clinical Practices (GCP) and relevant standards.Assists with the review and determination of appropriate site and vendor selection and ensures all vendors meet predetermined program milestones.
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