Job Description Main purpose of the job: To provide specialist care focused scientific and technical support to European medical affairs and marketing activities and to support/prepare the launch activities for other products To Design, implement and manage sponsored Phase IV studies and data generation within European markets and coordinate affiliate generated data review and approval process (IIT). <br /...
Based in Hemel Hempstead, Hertfordshire, out client is currently looking to recruit a Quality Co-ordinator to cover a maternity contract for one year. The organisation work in a very specialist, regulated environment and they are a leader in their field. You will be expected to be a highly organised individual who has a solid background in administration. You will thrive on working to deadlines which are always to very strict tim...
Job Description Responsible for the quality and regulatory compliance for studies in Start-up Phase. Perform SSU Project Team Management activities, coordinate the efforts of SSU Team Members and maintain clear client and internal team communication, process documentation, and compliance with Good Clinical Practices and procedures set forth by The Company and its clients. • Organizes efforts of team members assig...
Hertfordshire Medical Device exprienced Quality Assurance Officer- 28-32K per annum Our client is a highly reputed and a very well established Medical Device business. They are an accredited ISO 13485 site, based in Hertfordshire. From very humble beginnings back in 70s they currently employ several thousand employees across EU, The US, Asia, the Mid East, Far East and Americas. A world class global employer their name resonates in ...
We currently recruiting for several vacancies as a Production Technicians to work on on our nightshift, dayshift and 12hour shift, 4days on 4days off. Dayshift - 6am-2pm, 2pm-10pm weekly rotating shift. Nightshift - 10pm - 6am We are looking for candidates, who ideally must possess a relevant degree, wishing to develop their career within a pharmaceutical environment. Training will be provided for the right ca...
Duties will include liaising with clients, setting up new projects on computer system, tracking projects being completed and recording results of investigations, preparing detailed client reports and maintaining client files. This vacancy is based in the United Kingdom. A fundamental part of our service is that you will be required to make a personal visit to our office to finalise any application made on-line.&nbs...
Job Description Responsible for the successful planning, implementation and execution of contracted clinical activity. Assures the accurate transfer of contracts from proposal through project completion. Functionally responsible for all team members throughout the duration of each clinical trial. Assures clear client communication, process documentation, and compliance with Good Clinical Practices and proc...
Job Description Experience required: (1) CDISC, including SDTM. (2) Minimum 5 years working in pharmaceutical or CRO environment. (3) Early phase clinical trials. (4) SAS programming (not just point-and-click programming in Enterprise Guide). (5) Ability to explain what validation involves, and why it is necessary. Job description: (1) SAS program developmen...
Pharmacovigilance Associate to join an expanding company in Hatfield, Hertfordshire. As Pharmacovigilance Associate you will be a Life Science graduate of Healthcare professional. The Pharmacovigilance Associate will be offered a salary in the region of £25,000 + benefits. Duties and Responsibilities: Evaluate and process ICSRs (Individual Case Study Reports) including duplicate...
Pharmacovigilance Associate to join an expanding company in Hatfield, Hertfordshire. As Pharmacovigilance Associate you will be a Life Science graduate of Healthcare professional. The Pharmacovigilance Associate will be offered a salary in the region of £25,000 + benefits. Duties and Responsibilities: Evaluate and process ICSRs (Individual Case Study Reports) including duplica...
Based in Hemel Hempstead, Hertfordshire, out client is currently looking to recruit a Quality Administrator to cover a maternity contract for one year. The organisation work in a very specialist, regulated environment and they are a leader in their field. You will be expected to be a highly organised individual who has a solid background in administration. You will thrive on working to deadlines which are always to very strict timesc...
Quality Systems Data Document Processor - Hertfordshire Opportunity : This job opportunity is for all the quality assurance systems documents controllers out there looking for a new position. This is a brand new potion that has become available for a growing medical device / pharmaceutical company. Your role as Quality Assurance Systems Data Document Processor / Controller based in Hertfordshire...
This new and exciting opportunity for an outstanding Quality Engineer will mean you working closely with the Quality team, suppliers and manufacturing to provide a top class Quality Engineering capability for the business. Focussing particularly on ground breaking innovative new products, utilising plastic moulded components you’ll be involved with supplier development activities to establish the specifications and acceptan...
Pharmaceutical Quality Assurance Associate GMP - Middlesex Opportunity : Are you currently working in quality assurance within the manufacturing medical device, pharmaceutical or related industry? Do you have a good understanding of GMP, dealt with CAPAs and deviations? Have you maintained quality systems? Want to work for an innovative company? Yes, then you do not want to miss out on this rol...
