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Study Site Management Specialist at IQVIA - ApplyBlast

Study Site Management Specialist

IQVIA

9 months ago

3.8 on Glassdoor

Frankfurt, Hesse, Germany

Hybrid

Full Time

Senior

0 applicants

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About this role

A senior regulatory/site activation lead at IQVIA overseeing regulatory input and site activation for multi-regional clinical studies and programs. The role supports study initiation and maintenance, contributes regulatory intelligence to program strategy, and liaises with cross-functional and regional teams to ensure compliance with international guidelines. It also supports business development and collaborates with Quality Management and study teams to meet project timelines.

Skills

Qualifications

Bachelor's Degree in Life Sciences

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.