Regulatory Affairs Assistant

About the role

Join PSI, a leading Contract Research Organization, as a Regulatory Affairs Assistant in Almaty. You will support the regulatory aspects of clinical research projects, ensuring smooth communication between project teams and regulatory bodies.

Key responsibilities

• Act as the primary contact for clinical project teams on regulatory matters.
• Prepare draft regulatory and ethics submission dossiers.
• Manage documents, including filing, processing, translation, and quality control.
• Update and maintain automated tracking systems, working files, and schedules.
• Organise meetings, prepare agendas, and record minutes.

Required profile

• College or university degree, or equivalent education and experience.
• Life‑science degree is a plus.
• Administrative experience, preferably in an international setting.
• Prior experience in clinical research is advantageous.
• Full professional proficiency in English, Kazakh and Russian.
• Strong planning, multitasking and teamwork abilities.

Required skills

• Proficiency in MS Office applications.

What we offer

• A full‑time permanent position within a global CRO.
• An inclusive, diverse work environment that values personal growth.
• Opportunities to contribute to innovative pharmaceutical projects.