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Data capturer vacancies in eastern cape – clinical trial assistant

,

R 300000 ZA Per annum

Job Description:

Perform logistic work to assist clinical monitoring activities timely and effectively to ensure that clinical research project goes smoothly.

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Job Responsibilities:

Trial Master File Management and Documents Filing;

Prepare and provide the standard ISF index and fold for all the study sites;

Daily Study Administrative Support;

File all the essential study documents delivered by CRAs into TMF timely. Do double check for the completeness and quality of all the important documents filing (approvals, ICF, etc);

Set up TMF binders for a specific study according to the information provided by CRAs/Project Leaders;

According to Tigermed SOP, be responsible for the management on the Trial;

Support Medical Director, Medical (associate) manager or supervisor on department daily management;

Assist medical director to organize and summary the weekly report in timely manner.

Department Administration Support;

Arrange proper archiving space to the TMF of each study and make proper label for clear identification according to Tigermed or sponsor SOP;

Master File kept in Tigermed office with the cooperation from CRAs/Project Leaders;

Job Requirements:

At least 1 year clinical trial related experience, CRO working experience is preferred. The excellent candidates will not be restricted to the current requirements;

Adequate knowledge of new product development, including local regulation, GCP, clinical trial operations;

Good skills on Microsoft Word, Excel, PPT and Outlook, etc.;

Good command of written and verbal English;

Bachelor degree or above in Medical, Pharmacology or Biology related major;

Other abilities such as Communication skills/Information-gathering skills. Knowledge and/or experience in medical practice is a plus.

Job Details:

Company: Tigermed

Vacancy Type: Full Time

Job Location: South Africa

Application Deadline: N/A

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