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© All Rights Reserved. ApplyBlast.com
Sitero
This role involves analyzing, reviewing, and interpreting safety data to author and review aggregate reports such as PSURs, PBRERs, and DSURs for submission to health authorities. The position requires managing process trackers, handling regulatory inquiries, and ensuring deliverables comply with regulatory requirements within agreed timelines. The incumbent will also contribute to training programs and collaborate with regulatory affairs to ensure appropriate reporting of pharmacovigilance information.
Sitero is a contract research organization (CRO) delivering next‑generation technology and services to accelerate clinical trials and research. They offer end‑to‑end solutions including clinical operations, IRB/IBC oversight, and drug safety/pharmacovigilance with a strong focus on regulatory compliance and participant safety. Sitero combines compliant technology platforms with experienced operational teams to shorten timelines, improve data quality, and de‑risk studies. Sponsors and research organizations partner with Sitero to unlock innovation and scale complex clinical programs.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
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
View leadership team, funding history,
and employee contacts for Sitero.
Sitero didn’t post a salary, so this is our estimate from similar listings.