Job Description: To assist with the performance of clinical trial related duties in the studies in accordance with Good Clinical Practice (GCP) standards. [the_ad id="21943"] Job Responsibilities: Ensure all queries are attended to appropriately and in a timely manner Discuss QC trends with study team during team meetings To pay particular attention to trends in the QC findings and to conduct refresher training where necessary Ensure a thorough understanding of the project protocol and the SSP manuals To conduct Quality Control activities for the clinical trials and train the site personnel in the protocol and its requirements Assist with regulatory communications, adherence and regulatory file review, Ensure the defined protocol is adhered to at all times. Participate in Project Team meetings as required and provide constructive feedback and support to other team members Maintain a positive and constructive partnership with study Investigators and other site staff through constructive feedback, provision of assistance and active problem solving Ensure all required protocol parameters are followed and recorded accurately at all times. Ensure study staff is following study standard operating procedures at all times. Job Requirements: Ability to apply consistent adherence to intentional research and GCP practices Good Computer Skills Good Clinical Practice (GCP) essential Attention to detail. Require good organizational, administrative and analytical skills. Delegation Qualification & Experience: Grade 12 and Degree in Science or Social Science or equivalent 5 years’ experience working in clinical trials together with previous QA/QC experience. Job Details: Company: Wits Health Consortium Vacancy Type: Temporary Job Location: Soweto, Gauteng, South Africa Application Deadline: N/A [the_ad id="21944"] Apply Here jobsrican.com
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