Base level role Perform comprehensive data management tasks including data review, query generation and query resolution. This may also include, but is not limited to creation of e CRF completion guidelines, entry of test data for e CRF and
IQVIA in South Africa is seeking a Base level Data Management professional to support clinical study data capture, review, query generation and resolution across study start-up, execution, database lock and close-out. The role requires a Bachelor’s degree in
IQVIA in South Africa is seeking a BASE level Data Manager to perform comprehensive data management tasks across study phases. You will review data, generate and resolve queries, support e CRF entry, and maintain TMF documentation. You’ll join diverse
Our client, a major player in the Insurance Space, is recruiting for Digital Performance Specialist. About the role The Digital Performance Specialist drives measurable growth across digital channels through data-led optimisation, campaign management, and actionable performance insights.
Join us on our exciting journey! IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. IQVIA offers a broad range of solutions that harness
We are seeking an experienced Senior Medical Writer to lead the development of high-quality clinical and regulatory documents supporting global regulatory submissions. This role plays a critical part in ensuring that documents such as Investigator’s Brochures
Overview IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. IQVIA offers a broad range of solutions that harness advances in healthcare information, technology,
At IQVIA, our Senior Project Managers play a pivotal role in bringing innovative medicines to patients worldwide. Youll provide strategic leadership for complex global clinical trials, partnering directly with sponsors and cross-functional teams to deliver studies
IQVIA is seeking a Principal Statistical Programmer to work remotely in South Africa. The role involves reviewing datasets for submission, designing SAS programs for complex clinical data analysis, and leading programming activities across clinical studies. Ideal candidates
The Clinical Trial Manager (CTM) will work collaboratively across cross-functional teams with Project Management, Clinical Operations, Data Management, Medical Monitoring, Pharmacovigilance, and Regulatory Affairs while understanding and managing client expectations. The Clinical Trial Manager is responsible for