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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