IQVIA

Senior Clinical Data Associate

South Africa · Work style not stated · Full time

Apply on the employer’s site ↗See how well you match this job

You apply directly with the employer. ROLIVA does not submit applications from this page and is not the employer.

About the role

Description from the employer’s posting. Check the employer’s page for the current version.

  • EmployerIQVIA
  • LocationSouth Africa
  • Work styleWork style not stated
  • Employment typeFull time
  • Employer posted

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

Show full description

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.

Staying safe while you apply

  • Never pay to apply, interview or accept an offer. ROLIVA never asks you for payment to apply to a job.
  • Apply only through the official “Apply on the employer’s site” button, on the employer’s own site, and check that a recruiter’s email uses that employer’s own domain rather than a free email address.
  • Be cautious of an offer made with no real interview, or pressure to decide quickly or share financial details early.

Does something look wrong with this listing? Use “Report broken link” in the role details, or read ROLIVA’s full job-safety guidance ↗.

Preparing for this role with ROLIVA

  • Check the fit.

    Compare the requirements with the experience you have confirmed, including gaps.

  • Prepare honestly.

    Build interview stories and application drafts from your own evidence.

  • Keep track.

    Save the role and record your own application status and follow-ups.

Create a free workspace or log in.

At a glance

  • Employment typeFull time
  • SenioritySenior
  • Employer posted
  • Added to ROLIVA
  • Last checked

Explore similar roles

Similar jobs