Quantitative Research Analyst providing analytical and data support to energy company's Grid Strategy team. Leveraging data analysis to support utility planning and decision - making processes.
About the role
- Clinical Research Associate supporting and overseeing clinical trial sites to ensure quality and compliance. Seeking experienced candidates in Johannesburg or Cape Town.
Responsibilities
- Conduct site selection, initiation, monitoring, and close-out visits in line with GCP and study requirements
- Support sites with recruitment planning and study training
- Monitor study progress, including regulatory submissions, enrollment, data quality, and query resolution
- Ensure proper maintenance of site files and TMF documentation
- Build strong relationships with site staff and collaborate with the study team
- Contribute to site-level financial oversight and start-up activities (where applicable)
Requirements
- Bachelor’s degree in a scientific or healthcare field (or equivalent experience)
- Minimum 2 years of on-site monitoring experience
- Experience in the following therapeutic areas are highly beneficial: Respiratory, Gastro Intestinal, Major Depression
- Strong knowledge of ICH-GCP and clinical research regulations
- Excellent communication, organization, and problem-solving skills
- Proficiency with Microsoft Office and digital tools (laptop, iPhone/iPad)
- Ability to work independently and build effective partnerships with sites and colleagues
Benefits
- Working at IQVIA
- Shape the Future of Clinical Research
- Support and oversee clinical trial sites
- Ensure highest standards of quality, compliance, and patient safety
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Tech skills
Location requirements
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