- Principal Clinical Study Specialist (Start-up) contract (Study/site set up documentation specialist)
Minimum 12 month contract position available for a Principal Clinical Study Specialist (start-up). This role emphasises on the regulatory documentation required to start a trial and is a very important position with our global pharma client. Daily rate available!!
- Study Start-Up Specialist I
The position provides study start-up activities in support of assigned projects.
- Senior Quality Specialist
Clinical Professionals are working with one of the Largest CROs in the UK, actively seeking experience Quality Specialists with expert working knowledge of Quality Management Systems and GMP regulations, to join them on a permanent basis.
- Principal Medical Writer - Homebased
This opportunity for a principal level Medical Writer will provide the successful applicant with a wide variety of projects and clients to work with, and also the line management and development of staff.
- QA Officer - 12 month Contract
QA Officer, 12 Month Contract, A great opportunity for a QA officer to be a part of a nationally known project on a contract basis for the next 12 months. The is a lab based position located within the South East of England. You will report and work directly with the QA Manager assisting in a number of areas including CAPA, Documentation, Deviations, SOP’s and more. ...
- Quality Assurance Auditor Warsaw Poland
Quality Assurance Auditor GCP, Warsaw, PolandExperienced QA professional required for a Quality Assurance (QA) Auditor position. This is an office based position in Warsaw. You will conduct audits of on-going clinical research and data management projects, as well as assist with handling other QA program initiatives. Permanent role.
- Quality Assurance Auditor Prague Czech Republic
Quality Assurance Auditor GCP, Prague, Czech Republic Experienced QA professional required for a Quality Assurance (QA) Auditor position. This is an office based position in Warsaw. You will conduct audits of on-going clinical research and data management projects, as well as assist with handling other QA program initiatives. Permanent role.
- Study Start-Up Associate - Home based - Turkey
Study Start-Up Associate - CRO - Istanbul Turkey This is an exciting role with one of the industry leading CROs. This is a home based role in Istanbul. This role is for someone with healthy experience in Clinical Research that has a strong interest in submissions and feasibilities. You will have an experienced background in Regulatory Affairs, Clinical Research or Study Start-Up.
- Sterility and QA Engineer
Sterility and Quality Assurance EngineerSterility and Quality Assurance Engineer required for a global Pharmaceutical manufacturing company. This is a permanent role based in big manufacturing site in East Anglia. You will be responsible for providing coaching to other functions in using problem solving structured approach to help support and lead risk reduction and continues improvement initiatives. Candidates must be eligible to work in the UK. ...
- Senior QA GCP Auditor
Senior QA Auditor, 6 - 12 Month Contract, Global CROI am currently working with a global CRO who are currently in search for a Senior Quality Assurance Auditor to join their team for 6 – 12 months. The position will be office based (Midlands) requiring less than 50% travel. ...