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Clinical Trial Associates
The Clinical Trial Associate provides logistical support for the day-to-day operations for one or multiple clinical trials from concept and onset through to completion. This position communicates with clinicians at various trial sites and ensures that all regulatory documents are properly maintained for all studies. Detailed and accurate reporting of all metrics, including all related payments, is critical for the Clinical Trial Associate, who must regularly communicate with the Clinical Trial Manager, Clinical Operations and vendors. The Clinical Trial Associate also coordinates meetings related to trials in addition to planning all meeting materials.
A four-year degree and clinical experience is required for this detail-oriented position. Regulatory Compliance training is required as are proficient computer skills, excellent communication and strong organizational skills.
Employment Outlook
Clinical Trial Associate career opportunities are typically found in hospitals, physicians’ offices, contract research organizations, biomedical research organizations and institutions, sectors of the government, and specialty disease centers and pharmaceutical and medical device suppliers. With the rapid growth of the healthcare industry, particularly in Biotechnology and Genetics, Clinical Trial Associate positions are expected to increase 14% or more in the next 10 years.
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