
Clinical Trial Associate
Maintaining the Trial Master File (TMF) and assisting with site management, initiating the distribution, collection, handling, reviewing, tracking and archiving of essential documents throughout the lifecycle of clinical studies. Assists the study teams with site communications for various purposes – this includes feasibility/site identification activities and site updates. Responsible for the submission of study documents to ethics committee and/or competent authorities; works as a liaison with review boards and independent ethics committees in the regulatory approval process. Assists with tracking of clinical study progress including the creation and maintenance of study related trackers and status reports. Performs review of clinical data listings, as required. Prepares for and attends Investigator Meetings, as required.
4-6 years of related experience
Knowledge of FDA Code of Federal Regulations and Good Clinical Practices
Time Management
MS Excel
MS Word
eTMF
EDC
Adaptable
Multitasking
Problem Solving
Verbal communication
Detail Oriented
written communication
Organizational skills
According to JobzMall, the average salary range for a Clinical Trial Associate in 550 Hills Dr, Bedminster, NJ 07921, USA is between $49,000 and $65,000 per year. The salary range for a Clinical Trial Associate can vary depending on the individual's experience, qualifications, and location.
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Aerie Pharmaceuticals Inc. is a publicly traded, clinical-stage pharmaceutical company focused on the discovery, development and commercialization of first-in-class therapies for the treatment of patients with glaucoma and other diseases of the eye.

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