A
Al Dibel
Admin Pharma
Skills
Compliance
2 months ago
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Important information
Contract type:
Permanent
Location:
Doha, Qatar
Work mode:
Onsite
Published on:
17 August 2026
What they need
- Manage and maintain all documentation related to drug development, clinical trials, and regulatory submissions, ensuring compliance with GxP standards.
- Coordinate and schedule meetings, manage calendars, and prepare agendas and minutes for key pharmaceutical committees and project teams.
- Process and track invoices, expenses, and purchase orders for the pharmaceutical department, ensuring accurate financial record-keeping.
- Assist in the preparation and formatting of reports, presentations, and scientific documents for internal and external stakeholders.
Desired Candidate Profile
- Bachelor's degree in a relevant field such as Life Sciences, Business Administration, or a related discipline.
- Minimum of 3-5 years of administrative experience, preferably within the pharmaceutical or biotechnology industry.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) and experience with document management systems (e.g., Veeva, SharePoint).
- Strong understanding of pharmaceutical industry terminology, regulatory guidelines (e.g., FDA, EMA), and Good Documentation Practices (GDP).
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