IQVIA
๐ About IQVIA
IQVIA is a global leader in clinical research services, healthcare intelligence, and advanced analytics. At IQVIA, we create powerful connections to accelerate innovation in the life sciences sectorโultimately enhancing patient outcomes across the globe.
๐งพ Job Summary
Are you passionate about clinical data and ready to be part of high-impact studies that shape the future of healthcare? IQVIA is hiring a Clinical Data Associate to join its world-class team in Bloemfontein. This hybrid role is perfect for individuals with data management expertise and experience in clinical trials.
๐ ๏ธ Key Responsibilities
As a Clinical Data Associate, your tasks will include:
โ๏ธ Perform comprehensive data management activities from start-up to close-out
โ๏ธ Review data, generate and resolve queries
โ๏ธ Participate in reconciliation of all data streams
โ๏ธ Attend study meetings and teleconferences
โ๏ธ Manage freeze and lock of eCRFs
โ๏ธ Perform QC of archival CRFs and close-out activities
โ๏ธ Track cleaning progress and provide status updates
โ๏ธ Ensure TMF compliance and maintain documentation
โ๏ธ May serve as subject matter expert and mentor junior CDAs
๐ Qualifications and Experience
โ๏ธ Education: Bachelorโs degree in a Health or Science discipline
โ๏ธ Experience:
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Base Level: 1โ3 years in data management
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Advanced Level: 3+ years in data management
โ๏ธ Required: -
Rave EDC system experience
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Experience in clinical research and clinical trials
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Strong project and vendor management skills
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Proficiency in Microsoft Office tools
โ๏ธ Knowledge of industry standards: CDISC, SDTM, CDASH (Advanced CDA level)
๐ค Why Work at IQVIA?
โ๏ธ Work in a diverse and globally distributed team
โ๏ธ Opportunities for growth and leadership
โ๏ธ Access to cutting-edge tools and industry innovation
โ๏ธ Flexible work-life balance in a hybrid environment
โ๏ธ A mission-driven company impacting global healthcare
๐ Find similar jobs at:
https://careerjunctionza.co.za/jobs/
๐ CV Tips for Clinical Data Associate Roles
๐ Highlight Relevant Tools: Emphasize experience with clinical data systems like Rave or Medidata.
๐ Showcase Metrics: Quantify your impact (e.g., number of studies managed, reduction in query time).
๐ Certifications: Include relevant clinical research certifications (e.g., CDISC, GCP, ICH guidelines).
๐ Demonstrate Global Readiness: Mention experience in cross-functional or global teams.
โ
Customize for Each Role: Tailor your CV to match the specific job description and responsibilities.
๐ Company Website: https://jobs.iqvia.com
To apply for this job please visit jobs.iqvia.com.
