Pharmaceutical Operations Specialist
2 settimane fa
- Set up, organize and maintain clinical study documentation (e.g., Main Study Files, CRFs, etc.) including preparation for internal/external audits, final reconciliation and archival;
- Assist project teams with trial progress tracking;
- Contact CRO for specific requests (e.g., enrollment updates, missing documentation, meeting arrangements, etc.);
You will work closely with the project teams to ensure timely completion of tasks and high-quality deliverables. A university degree in Medical Science or a related field is required, along with a minimum of one year's experience in the Pharmaceutical, Biotechnology, and/or CRO industry.
We offer a dynamic and supportive work environment, with opportunities for professional growth and development. Apply now to take your career to the next level
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