Clinical Data Associate

**Summary of the Position**: The Clinical Research Associate II (CRA II) manages clinical study sites and monitors site activities to assure adherence to Good Clinical Practices (GCPs), Standard Operating Procedures (SOPs), study protocols, and applicable regulatory requirements. Reviews regulatory documents as required and prepares site visit reports. May...

A global clinical research provider is seeking an Advanced Clinical Data Associate in Centurion, South Africa. The role involves providing updates on project status, acting as a liaison for the Clinical Data Manager, and mentoring staff. The ideal candidate should possess a Bachelor’s degree in Health or Science, with over three years of experience in data...

Advance level roleProvide timely status updates including issues & risks to DM and DMLs as neededAct as the Point of contact for Clinical Data Manager, working pro-actively to identify risks and provide mitigationsMay communicate with the vendors to resolve reconciliation issues.Provide input to Study set up activities including but not limited to creation...

Base level rolePerform comprehensive data management tasks including data review, query generation and query resolution.   This may also include, but is not limited to creation of eCRF completion guidelines, entry of test data for eCRF and the Data Review Model, testing of data validation rules, etc.  Data Management tasks should be inclusive of Study...

Centurion, South Africa | Full time | Hybrid | R1517767 - **Job available in additional locations** Advance level role - Provide timely status updates including issues & risks to DM and DMLs as needed - Act as the Point of contact for Clinical Data Manager, working pro-actively to identify risks and provide mitigations - May communicate with the vendors to...

We are currently looking for talented **Senior** **Clinical Research Associates to join our team in South Africa**. You would be working within our Flexible Solutions department dedicated to one sponsor/client. Would you like to work for one of the best known big pharma companies? Our sponsor is a global mid sized pharma company with high working standards....

IQVIA is looking for a **Senior **Clinical Research Associate. **Job Overview** Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. **Essential Functions** - Perform site monitoring visits...

**Summary of the position**: **Essential Functions**: - Contribute to the development and review of protocols and their amendments. - Answer trial-related medical questions and interact with project team members such as Project Managers, Clinical Operations, Regulatory Affairs and Data Management colleagues, investigators, and other site personnel on...

**Summary of The Position**: The Contract Statistical Programmer will perform statistical and database programming (typically in SAS) related to clinical projects undertaken by FHI Clinical, according to the relevant trial protocol and other trial-related documentation, ICH GCP (and local adaptations thereof), local legal requirements, relevant FDA, EMA, and...

**Summary of The Position**: The Statistical Programmer will perform statistical and database programming (typically in SAS) related to clinical projects undertaken by FHI Clinical, according to the relevant trial protocol and other trial-related documentation, ICH GCP (and local adaptations thereof), local legal requirements, relevant FDA, EMA, and other...