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CRA 2, IQVIA Biotech at IQVIA - ApplyBlast

CRA 2, IQVIA Biotech

IQVIA

1 day ago

3.8 on Glassdoor

Reading, England, United Kingdom

Onsite

Full Time

Junior

0 applicants

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About this role

This role involves performing site monitoring visits and managing study progress for clinical trials in collaboration with sites and study teams. The position requires ensuring regulatory compliance, tracking subject recruitment, and maintaining essential study documentation. It is designed for professionals passionate about innovation in the biotech and biopharma sectors.

Responsibilities

Perform site monitoring visits in accordance with GCP and ICH guidelines
Track subject recruitment plans and manage study progress
Maintain Trial Master File and Investigator Site File documentation

Skills

About IQVIA

iqvia.com

Headquarters

Durham, North Carolina, United States

Company Size

10001+ employees

Founded

2016

View Profile

IQVIA is a leading global provider of data, technology, and advanced analytics focused on transforming healthcare and life sciences. The company empowers organizations to accelerate innovation, enhance patient outcomes, and expedite the market introduction of new treatments through comprehensive healthcare analytics and real-world evidence. With a commitment to Human Data Science, IQVIA combines its extensive expertise with innovative technology to improve health outcomes worldwide.