Clinical Trial jobs
View similar jobs with this employerIQVIACenturion, Gauteng- Data Management experience and experience working on a clinical trial mandatory.
- Bachelor’s degree in a Health or Science discipline with experience in clinical…
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- Background in clinical trial management.
- Experience with clinical trial submissions in other Southern African Countries - preferred.
- TASKParow, Western Cape
- Planning, coordinating, implementing and participating in recruitment campaigns according to clinical trial protocol requirements.
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- StrykerJohannesburg, Gauteng 2160
- Coordinate and conduct product trials and evaluations in theatre and clinical environments, supporting evidence‑based product adoption.
- ICON PlcJohannesburg, Gauteng
- Collaborating with cross-functional teams, including clinical project managers, data managers, and biostatisticians, to ensure the successful execution of…
- IQVIABloemfontein, Free State
- Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e.
- Good software and computer skills.
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View similar jobs with this employerIQVIACenturion, Gauteng- Serve as Data Team Lead (DTL) on a program of 6-10 global clinical trials or 40+ increasingly complex central laboratory studies.
- SOW (scope of work) / budget.
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View similar jobs with this employerIQVIACenturion, Gauteng- Lead data management for complex, global clinical trials from study setup to database lock.
- IQVIA is seeking experienced Clinical Data Management Leads to…
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- Salary Search: Clinical Data Management Lead salaries
- See popular questions & answers about IQVIA
View similar jobs with this employerIQVIACenturion, Gauteng- Lead data management for complex, global clinical trials from study setup to database lock.
- IQVIA is seeking experienced Clinical Data Management Leads to…
- View all IQVIA jobs - Centurion jobs - Clinical Data Manager jobs in Centurion, Gauteng
- Salary Search: Clinical Data Management Lead salaries
- See popular questions & answers about IQVIA
- TOTAL TRIALS INCCenturion, Gauteng
- Support the Finance Manager with the management of the company’s financial affairs, in accordance with sound financial management and accounting practices.
- 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.
- TrialfactsHome Based
- Client Onboarding & Support: Guide new clients through our onboarding process, ensuring they feel confident using our systems and understand how we help them…
- ClarinessCape Town, Western Cape
- Impact healthcare by accelerating medical innovation through improved access to clinical trials, potentially bringing needed treatments to patients faster.
- Syneos - Clinical and Corporate - ProdHome Based
- Participates in and may lead global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical…
Technical Support Manager - Farm Animals
Often replies in 12 daysVirbacCenturion, Gauteng- Assist in defining, planning and overseeing Marketing trial needs as product support strategies (marketing trials) to illustrate ROI to customers and the…
- TASKBellville, Western Cape
- Previous experience in clinical trials, preferably in a coordinator or similar role.
- Ensuring strict adherence to study protocols, regulatory guidelines,…
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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.