Clinical Data Associate - Base

3 LOCATIONS, OTHER (OTHER)HYBRIDPOSTED: 6/28/2026
PHARMAFull-time
HIRING ORGANIZATIONIQVIAHealthcare Technology & Contract Research
Iqvia

ROLE DEFINITION & RESPONSIBILITIES

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.

REQUIRED VERIFIED SKILLS

Clinical Research
Microsoft Office
Project Management

COMPENSATION & REWARDS

Salary: Competitive / Disclosed upon candidate shortlisting
Salary for this Clinical Data Associate - Base position is competitive and aligned with industry standards for this location.

ORGANIZATION CONTEXT & CULTURE

IQVIA is a leading global provider of advanced analytics, technology solutions, and contract research services (CRO) to the life sciences industry. The company helps pharmaceutical, biotech, and medical device clients accelerate the development and commercialization of new medical treatments through its extensive data, technology, and human expertise. Their offerings span from clinical trial design and execution to real-world evidence and commercial effectiveness.

TEAM SIZE: 87,000+ employees
INDUSTRY: Healthcare Technology & Contract Research

EXPECTED CAREER ROADMAP

Clinical Data Associate ➔ Senior Data Manager ➔ Clinical Data Lead ➔ CDM Director.

APPLICATION ADVISORY

Ensure your resume clearly showcases experience with: Clinical Research, Microsoft Office, Project Management. Prepare real-world examples demonstrating these skills for the interview.

READY TO SUBMIT?

Verify your capability profile and matching credentials before submitting direct applications.