Site Coordinator
psicro
Regulatory Officer (Clinical Trial Submissions)
psicro· Regulatory
About this role
Company Description
PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications.
At PSI, we foster an environment where a diverse range of colleagues feel welcomed and valued. Our inclusive culture is a cornerstone of our success, enabling us to attract and retain top talent globally.
We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry.
Job Description
Join our team of experts in regulatory and ethics submissions of clinical studies. You will focus on facilitating the start of research projects of novel medicinal products in Kazakhstan, while taking a step further in your professional career.
Office-based in Almaty
You will:
- Prepare clinical trial submission dossiers for Regulatory and Ethics Authorities, including Import and Export license applications
- Communicate with regulatory authorities, ethics committees, project teams and vendors on regulatory-related matters
- Review translations of essential documents subject to clinical trial submission
- Track the regulatory project documentation flow
- Review documents to greenlight IP release to sites
- Manage safety reporting to authorities
- Deliver regulatory training to project teams
- Assist with feasibility research and business development requests
Qualifications
- College/University degree or an equivalent combination of education, training and experience
- Clinical trial industry experience
- Prior experience with clinical trial submissions in Kazakhstan
- Full working proficiency in English and Kazakh
- Proficiency in MS Office applications
- Detail-oriented
- Ability to learn, plan and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
Additional Information
If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you.
Frequently Asked Questions
Is the salary disclosed for the Regulatory Officer (Clinical Trial Submissions) position at psicro?
The salary for this Regulatory Officer (Clinical Trial Submissions) role at psicro is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the Regulatory Officer (Clinical Trial Submissions) position at psicro located?
This Regulatory Officer (Clinical Trial Submissions) role at psicro is based in Almaty, Almaty, Almaty Region, Kazakhstan, Almaty Region, kz. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the Regulatory Officer (Clinical Trial Submissions) role at psicro full-time or part-time?
This is listed as a Full time position. It is posted as a Regulatory Officer (Clinical Trial Submissions) role in the Regulatory department at psicro.
Which team or department does the Regulatory Officer (Clinical Trial Submissions) at psicro belong to?
This Regulatory Officer (Clinical Trial Submissions) position is part of the Regulatory department at psicro. See the full job description for more information about the team structure and responsibilities.
How do I apply for the Regulatory Officer (Clinical Trial Submissions) position at psicro?
Click the "Apply Now" button on this page. You will be redirected to psicro's official application portal hosted on smartrecruiters where you can submit your application directly.
When was the Regulatory Officer (Clinical Trial Submissions) job at psicro posted?
This Regulatory Officer (Clinical Trial Submissions) position at psicro was posted on Jul 21, 2026. Apply as soon as possible — early applications are often reviewed first.
Regulatory Officer (Clinical Trial Submissions)
psicro
You'll be redirected to psicro's official application page on SmartRecruiters.