London, Londonderry - Northern Ireland, United Kingdom
-
Full Time
Start Date
Immediate
Expiry Date
21 Dec, 26
Salary
50000.0
Posted On
22 Sep, 26
Experience
10 year(s) or above
Remote Job
Yes
Telecommute
Yes
Sponsor Visa
Yes
Skills
Industry
Pharmaceutical Manufacturing
Description
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.
Responsibilities
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.
Linked-in
Google