Data Capturer Vacancies in Eastern Cape – Clinical Trial Assistant

Website Tigermed

Job Description:

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

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

Apply Here