Regulatory Officer (Clinical Trial Submissions)

PSI CRO

3 hours ago

Almaty, Almaty Region, Kazakhstan

Onsite

Full Time

Junior

0 applicants

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About this role

A Regulatory Specialist at PSI focuses on facilitating the start of research projects for novel medicinal products in Kazakhstan, ensuring regulatory and ethical compliance through submission dossiers, communication with authorities, document review, and safety reporting.

Skills

Qualifications

College/University degreeClinical trial industry experiencePrior experience with clinical trial submissions in KazakhstanFull working proficiency in English and KazakhProficiency in MS Office applications

About PSI CRO

psi-cro.com

PSI CRO is a full-service global Contract Research Organization (CRO) that partners with biopharma and medical device sponsors to plan and run clinical trials. The company emphasizes predictable patient enrollment across multiple therapeutic areas and offers end-to-end services such as study operations, site management, monitoring, and regulatory support. With a worldwide footprint and local operational expertise, PSI positions itself as a trusted, reliable partner for delivering clinical development programs on time.