Deliver CTA regulatory strategies and operations for a designated portfolio of development compounds in specified geographic region.
Ensure the submission strategy for clinical trials planned globally are in accordance with the overarching global regulatory strategy and any risks and issues are highlighted to the Global Regulatory Project Team and study teams.
General
SRG are currently looking for a Regulatory Affairs Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory Affairs team on an initial 12 Month basis to be based at their office in Maidenhead.
An excellent opportunity has arisen for an Order Processerto join our friendly team based in Sittingbourne or Maidenhead.
Job: H2H Order Processer (6 months contract)
Our client manufactures specialist medical food and equipment for enterally (through tubes) fed patients, to improve patient quality of life and meet their nutritional needs.
This role has come about due to expansion and an increase in the production of pharmaceutical.
This is an excellent opportunity for an experienced Clincial Trial Regulatory Specialist to join a global pharmaceutical company for an initial 12 months with the potential for this to be extended.
This role has come about due to expansion and an increase in the production of pharmaceutical.
This is an excellent opportunity for an experienced Clinical Trial Submissions Manager to join a global pharmaceutical company for an initial 12 months with the potential for this to be extended.
To collate, check and process monthly information for the payroll including starters, leavers, timesheets, attachment of earnings and child maintenance orders, sickness, expenses, shift enhancements and pensions.
General
An experienced, professional, and competent individual is required immediately on a fixed term contract basis.
An exciting opportunity has arisen for a Payroll & Pensions Manager to join a well-established company based in Maidenhead.