Clinical Trial Assistant Job Description

Clinical Trial Assistant Job Profile and Description

A clinical trial assistant is someone who is responsible for helping in the overall performing of a clinical research trial process.

Duties and Responsibilities

• A clinical trial assistant has to help the main investigator, scientist or physician who is responsible for the overall performance of the trial.

• He has to accurately track and maintain the clinical systems of the trial and check to see whether project timelines and track site compliance is being met.

• He has to help the staff assigned with the trial to prepare, handle, distribute, file, and archive the clinical documentation of the trial.

• He has to ensure that standard operating procedures are being met during the trial.

• He has to provide assistance in tracking and managing the CRF’s, clinical data flow and other queries of the trial.

• He has to prepare, handle and distribute the Clinical Trial Supplies and maintain tracking information.

• He has to be the central contact of the clinical trial team in all communications, documentations and correspondence.

• He may have to involve himself in performing certain administrative functions as well to support the trial team.

Skills and Specifications

• A clinical research assistant needs to be able to work on his own.

• He must be equipped with excellent planning, problem – solving and organizational skills.

• He must possess very good interpersonal and communications skills to be successful in this profession.

• He must be proficient is using the computer.

• He must have good teamwork ability.

• He must also possess very high analytical and negotiating skills.

Education and Qualifications

A clinical research assistant must have an advanced degree in his field of interest, such as a PhD, MD or Pharm. D. Interest in research work is also a must in this field.

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Filed in: Research Job Description
Tagged with: Assistant Duties • Clinical Trial • Job Description