Regulatory CMC/Documentum Contractors-12 months Based Herts/North London Based in Potters Bar, Herts (15 minutes from Kings Cross), Mylan has global revenues of $6.8 billion, a commercial presence in all EU and international regions and a robust, diverse portfolio of blockbuster products across all dosage forms. The substantial EU Regulatory Teams in the UK need support to manage the strategic compliance and g...
Job Description: Our client is a growing CRO who are looking for a Principal Statistical Programmer to be based in their Slough office. Job Summary Provides programming and technical support to allocated studies within agreed project timelines. Communicates programming related study issues to the Study Statistician. Acts as Study Statistician as required. Participates in business development and client li...
Contract CRA/SCRA Category: Pharma Type: Contract Location: South West- UK Daily Rate: £200-£270 Are you a competent clinical research associate looking for a new contract position? If so I’m working with a client that you need to know about. My client is one of the most reputable pharma companies in the world and has been recognised as being one of the best places to work globally....
Test Lead Location: Dublin Rate: Dependant on experience Duration: 4 months Job Type: Contract The role I am currently seeking a Test Lead for my client in Dublin. The successful candidate will be working in an agile/scrum development methodology. My client is looking for someone who will proactively...
An exciting opportunity has arisen for a Senior Financial Analyst to work within the Financial Planning and Analysis Team on a 6 month contract for my Client based in Cambridge. You will be a Qualified Accountant (CIMA / ACCA with Shared Financial Services Experience), You will be Strong on Systems: Cognos, Hyperion & Oracle, & Advanced Excel. Reporting to the FPA Manager your duties will include: co-ordinating the plan...
I am looking for a Interim Quality Assurance Manager working for a leading Pharmaceutical organisation. This role will be overseeing the QA department for approximately 3 months. You will have responsibility for the UK GxP requirements with a particular focus on GDP. You will be overseeing a more junior member of staff. As a contractor you will play an important role working closely with the RP to ensure products are distributed and...
UK Interim Brand/Product Manager, Urgent Requirement Innovative Pharmaceutical Company London. 6 to 12 month contract, 3 to 5 days a week. To c£400 to £450pd (DOE). My client is urgently seeking an interim brand manager for a 6 to 12 month contract to come in and support the existing brand teams working on one of their leading brands within mental health. The Company One of the fastest growing pharm...
Regulatory Affairs - 6-9 month contract - Medical Devices Due to plans to expand into new markets this exciting and highly intelligent business now needs a Regulatory Specialist to aid the completion of 510k submissions and product registrations, this role is based in Berkshire. Working closely with the RA/QA manager, the successful individual will be completing regulatory activities that are essential for the business to ...
Senior Quality Engineer (Medical Device / Product Transfers), NW UK, 12 mth contract, Daily Rate negotiable, This position supports the transfer of products between manufacturing sites, ensuring acceptance criteria are established and robust verification and validation activities are performed. This position is a key member of product transfer teams and interfaces between the 'sending site’ and 'receiving site’ accord...
Statistician - Clinical - Statistics - Surrey - Contract As a Clinical Statistician you will be managing statistical project support and providing expert statistical consultancy across the function. You will also liaise and work closely with Medical Directors on the statistical analysis and reporting of clinical trials. Responsibilities also include: Providing expert review of study designs, analysis plans and r...
Statistician to analyse and report on statistical data from clinical trials. Communicate your findings effectively with directors and senior memebers of staff. You must have at least 5 years SAS 9.2 ideally from a clinical trials environment and excellent interpersonal skills. 12 month contract intially. ...
