Provide end‑to‑end administrative and operational support for RUBCCA Life Sciences activities to ensure timely, compliant, and efficient execution of internal processes.

Support organization and execution of local clinical trials and research activities, including coordination of tenders, documentation, and external partners, to enable compliant delivery of studies.

Maintain structured and up‑to‑date archiving of Life Sciences administrative, research, and technical documentation to support traceability and audit readiness.

Deliver competitor and market monitoring inputs upon request to support Life Sciences, regulatory, and business discussions.

Support development, translation, and adaptation of internal education and communication materials to ensure scientific accuracy and consistency.

Provide ongoing operational support for nutrition‑ and science‑related data requests (e.g., pep+ positive choices status, marketing materials review – e.g. web-site articles etc.) to enable timely and accurate responses to global and local stakeholders.

University degree. Dergee in Life sciences, biology, pharmacy, or a related scientific field is an advantage.

3+ years of experience in an administrative or operational support role within Life Sciences, R&D, Regulatory Affairs, or a comparable regulated environment.

Solid understanding of document workflows, approval processes, and compliance requirements in a corporate setting.

Experience supporting clinical trials, local research activities, or working with external research partners is an advantage.

Strong organizational skills, attention to detail, and ability to manage multiple tasks and stakeholders.

Professional proficiency in English and Russian.