Regulatory and Start Up Admin
IQVIA
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
About IQVIA
iqvia.comIQVIA 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.
Recent company news
Insider MonkeyJim Cramer on IQVIA: “I Like the Business Very Much, I Just Don’t Know Whether This Is the Right Stock to Play It”
6 hours ago
Business WireIQVIA Releases its 2025 Sustainability Report
4 days ago
MarketBeatIQVIA Holdings Inc. $IQV Shares Bought by Elo Mutual Pension Insurance Co
1 day ago
Stock TitanIQVIA finance chief's talk to stream from Barclays global healthcare conference
2 days ago
Seeking AlphaIQVIA Holdings: Still Exceeding Expectations As A Stealth Compounder (NYSE:IQV)
4 days ago
About IQVIA
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Leadership Team
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
Unlock Company Insights
View leadership team, funding history,
and employee contacts for IQVIA.
Salary
$38k – $52k
per year
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