Medical Research jobs in Gauteng
- IQVIACenturion, Gauteng
- Bachelor’s degree in a Health or Science discipline with experience in clinical research.
- Experience working in highly diverse teams within clinical research;…
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- Salary Search: Clinical Data Associate - Base salaries
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- Clinix Health Group (Pty) LtdSandton, Gauteng
- Registration with HPCSA as a medical practitioner.
- Research, enable and consult on opportunities to harness medical technology in the treatment of clients.
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- Salary Search: Medical Officer salaries
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- TOTAL TRIALS INCCenturion, Gauteng
- Apply medical knowledge and experience to the review and assessment of medical and safety data during trial conduct and post-trial analysis.
- Business Dynamics ConsultantsPretoria, Gauteng
- Identify and attract medical and healthcare professionals for international opportunities, including doctors, nurses, allied health professionals, specialists,…
- ICON PlcJohannesburg, Gauteng
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
- Your focus will be on coordinating clinical trial monitoring…
- IQVIACenturion, Gauteng
- Previous experience with medical writing is essential for the role.
- Contribute to medical writing training initiatives to upskill the team and set quality…
- University of PretoriaPretoria, Gauteng
- UP subscribes to the BESTMED and UMVUZO medical aid schemes and contributes 50% of the applicable monthly premium.
- Strong display of customer service acumen;
- View all University of Pretoria jobs - Pretoria jobs - Human Resources Administrator jobs in Pretoria, Gauteng
- Salary Search: Faculty of Economic and Management Sciences: Human Resource Management Department - Departmental Administrator B salaries in Pretoria, Gauteng
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- IQVIACenturion, Gauteng
- Principal Data Manager position is to oversee data operations tasks for a team of data managers from study start-up to database lock, to produce a clean and…
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View similar jobs with this employerSouth African Medical Research CouncilPretoria, Gauteng- Create research translation outputs such as policy briefs and media output.
- A PhD qualification in epidemiology / biostatistics / data science/ medical…
- IQVIACenturion, Gauteng
- Oversees the development of research questions, PICOS criteria, search strategies and literature review protocols.
- Proficiency in MS Word, PowerPoint, Excel.
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- Eli LillyJohannesburg, Gauteng
- Support the design of customer research as medical expert.
- Support medical information associates in preparation and review of medical letters and other medical…
- Eli LillyJohannesburg, Gauteng
- Support the design of customer research as medical expert.
- Support medical information associates in preparation and review of medical letters and other medical…
- KearneyJohannesburg, Gauteng
- Comprehensive medical insurance for employees and their families.
- Support with research requirements for the projects, as required.
- LexisNexisJohannesburg, Gauteng
- Provide insight and research on competitive intelligence, market sizing, industry trends, regulatory trends and market drivers to inform strategy and improve…
- LexisNexis Risk SolutionsJohannesburg, Gauteng
- Provide insight and research on competitive intelligence, market sizing, industry trends, regulatory trends and market drivers to inform strategy and improve…
- ClickatellJohannesburg, Gauteng
- O Documentation: Document research findings, design concepts, and development processes to maintain a clear and organized record of innovation efforts.
Job Post Details
Clinical Data Associate - Base - job post
Location
Full job description
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 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 Start-up, Execution, Database Lock and Close-out.
- Perform ongoing Data Reconciliation of all data streams
- Attend study related meetings/teleconferences
- Perform Study Closeout/Archiving Activities including QC of subject/site Archival CRFs
- Create and provide status/metric reports
- Generate reports on EDC and track cleaning progress
- Manage Freeze / lock of eCRF
- File documentation in the virtual Trial Master File (TMF)
- Receives and enters lab normal ranges
Education and Experience Guidelines:
- Bachelor’s degree in a Health or Science discipline with experience in clinical research.
- Data Management experience and experience working on a clinical trial mandatory.
- Rave experience mandatory
- Experience working in highly diverse teams within clinical research; cross-functional, global, multi- regional.
- Knowledge of current industry standards (e.g., CDISC, SDTM, CDASH, etc.) for Advanced CDA.
- Knowledge of technology platforms and systems to capture and process data
- Project management skills.
- Vendor management skills.
- Proficiency with Microsoft Office tools
- Experience CDA BASE level: 1-3 years of experience in Data Management at a CRO/Pharma
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.