Clinical Data Associate

IQVIA Argentina; Manchester; On-site; GBP 26,000 - 36,000; Full time

Job summary

IQVIA's Medicines Evaluation Unit in the UK seeks a Clinical Data Associate to support data entry, query resolution, and admin tasks within a hospital-based trial environment. This office-based role focuses on accurate data capture and timely documentation.

You will assist with volunteer logistics, support sponsor monitoring visits, manage database updates, and help with archiving, contributing to high-quality data for multiple therapeutic areas.

Qualifications

• High School Diploma required.
• Proficient in Word, Excel, PowerPoint.
• Strong written and verbal English communication.
• Basic data entry and administrative skills.

Responsibilities

• Perform clinical trial data entry with accuracy.
• Resolve data queries and ensure data quality.
• Provide administrative support to the data management team.

Skills

Communication skills

English language

Attention to detail

Education

High School Diploma

Tools

Microsoft Office

Word

Excel

PowerPoint

Job description

Clinical Data Associate

Medicines Evaluation Unit (MEU)

This role is office based!

The Medicines Evaluation Unit (MEU) Ltd, an IQVIA business, is one of the UK’s leading contract research organisations, and a facility where commitment to excellence is paramount. Possessing extensive pharmaceutical, scientific and clinical expertise, allied with fast volunteer recruitment, both healthy and patient, within a state-of-the-art hospital based research facility, enables the MEU to offer clients positive clinical trial solutions.

Join us on our exciting journey!

Job Overview:

Serve in support-level capacity on a Clinical Data Management team to provide efficient, quality data entry, query resolution, and administrative services that meet customer needs.

Responsible for clinical trials data entry.

Responsible for the administration of volunteer logistics.

Assisting with clinical trial administrative duties.

Responsible for assisting at sponsor monitoring visits.

Assist with database updating / other data related activities.

Responsible for archiving duties.

Requirements:

• High School Diploma or equivalent
• Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
• Written and verbal communication skills including good command of English language.

Join IQVIA to see where your skills can take you

• High level of autonomy.
• Global exposure
• Variety of therapeutic areas
• Collaborative and supportive team environment
• Access to cutting-edge and innovative, in-house technology
• Excellent career development and progression opportunities
• Work-Life Balance, with a strong focus on a positive well-being.

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.