Jobsrican
Website Wits Health Consortium
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
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