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Regulatory and Start Up Admin at IQVIA - ApplyBlast

Regulatory and Start Up Admin

IQVIA

7 months ago

3.8 on Glassdoor

Prague, Czech Republic

Onsite

Full Time

Trainee

0 applicants

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About this role

A Clinical Trial Submission Support role at IQVIA involves assisting with the preparation, management, and tracking of clinical trial submissions and notifications within CTIS and CTMS systems. The role supports regulatory activities for clinical trials, ensuring documentation accuracy, timely submissions, and coordination among trial teams.

Skills

Qualifications

1 year clinical research experience

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.