Global Channel Management, Inc.
Clinical Operations 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 but at the same time require the best talent for the job.Qualifications
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.Extensive knowledge of clinical development principles, theories, and concepts with a high degree of comprehension of pharmaceutical industry practices, standards, and GCPs.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.Excellent written and oral communication skills, with the ability to communicate in medical and scientific terms with vendors, consultants, and peers.Ability to read, analyze, and interpret professional journals, technical procedures, and government regulations. Ability to write reports, business correspondence, and procedures.Ability to solve problems and deal effectively with a variety of variables in situations of limited standardization.Must be tactful, mature, flexible, and have well-developed interpersonal skills, able to work independently and in a team, multi-task, and prioritize to complete assignments on time, and coach and manage the efforts and development of direct reports.
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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.Extensive knowledge of clinical development principles, theories, and concepts with a high degree of comprehension of pharmaceutical industry practices, standards, and GCPs.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.Excellent written and oral communication skills, with the ability to communicate in medical and scientific terms with vendors, consultants, and peers.Ability to read, analyze, and interpret professional journals, technical procedures, and government regulations. Ability to write reports, business correspondence, and procedures.Ability to solve problems and deal effectively with a variety of variables in situations of limited standardization.Must be tactful, mature, flexible, and have well-developed interpersonal skills, able to work independently and in a team, multi-task, and prioritize to complete assignments on time, and coach and manage the efforts and development of direct reports.
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