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Senior Clinical Data Associate

Bloemfontein, South Africa

Pay
Pay not listed
Work setting
Not stated
Employment
Full-time — employment source
Employment type in the employer’s posting: Full time
From the employer’s posting
Apply at Iqvia

What you’ll work on

Full posting
  • Coordinate and assign work to CDAs on a study alongside the Global Data Manager

  • Send timely status updates on issues and risks to DM and DMLs

  • Act as point of contact for the Clinical Data Manager and proactively identify risks

  • Help set up studies, including inputs to DVRs and data management documents

  • Train and mentor CDA staff

From the employer’s posting
Assign work to allocated CDAs on a trial.
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
Provide input to Study set up activities including but not limited to creation of DVRs
Train and mentor CDA staff

What you’ll bring

All qualifications

Core experience

  • Bachelor's degree in a Health or Science discipline with clinical research experience
  • More than 3 years of data management experience, including on a clinical trial
  • Rave experience
  • Knowledge of industry standards such as CDISC, SDTM and CDASH
  • Project management and vendor management skills
Qualification wording
Bachelor’s degree in a Health or Science discipline with experience in clinical research.
>3 year of experience Data Management experience Data Management experience and experience working on a clinical trial mandatory.
Rave experience mandatory
Knowledge of current industry standards (e.g., CDISC, SDTM, CDASH, etc.) for Advanced CDA.
Project management skills. Vendor management skills.
Education & alternatives
Education and Experience Guidelines: - Bachelor’s degree in a Health or Science discipline with experience in clinical research. - Experience CDA ADVANCED level: >3 year of experience Data Management experience

Posting record

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Status in our records
Live
First seen by us
Oct 9, 2026 · 20 days ago
Recorded sightings
70
Last seen by us
Oct 29, 2026

These dates show when we found the posting. Check the employer’s website to confirm it is still accepting applications.

Your next step

  • Have your resume and examples of relevant work ready.
  • Check the listed location, eligibility and core experience before starting.
  • Ask the employer about the pay range before committing time to the process.

Complete your application on iqvia.wd1.myworkdayjobs.com. The employer’s form will show what is required.

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Job description

View original posting ↗

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 resolve reconciliation issues.

  • Provide input to Study set up activities including but not limited to creation of DVRs

  • Create and/or provide inputs to Data Management documents (e.g. eCRF completion guidelines, etc.).

  • Review and provide inputs to Data Management documents (e.g. IRP, DMP, etc.)

  • Assign work to allocated CDAs on a trial.  Coordinate work of CDAs assigned to a study working closely with the Global Data Manager to understand priorities and timelines.

  • Assist the Data Management Leader in TMF compliance reviews.

  • Train and mentor CDA staff

  •  May serve as an SME and participate in SME forums

  • May act as delegate for Data Manager, as needed

Education and Experience Guidelines:  

  • Bachelor’s degree in a Health or Science discipline with experience in clinical research. 

  • Experience CDA ADVANCED level:  >3 year of experience Data Management experience

  • 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

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.

Source details

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Location & working pattern

Bloemfontein, South Africa

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