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Quality assurance auditor - ireland
- Plan and conduct QA Clinical audits on a regional basis - Ensure that audit results are formally and consistently recorded, reported and then corrective/preventative actions have been requested. - Review audit replies to QA
Quality assurance auditor - ireland
- Plan and conduct QA Clinical audits on a regional basis - Ensure that audit results are formally and consistently recorded, reported and then corrective/preventative actions have been requested. - Review audit replies to QA
Senior clinical data manager
Clinical Professionals-Berkshire/Buckinghamshire - Berkshire/Buckinghamshire-United KingdomContract : Permanent - Salary : £Negotiable + BenefitsSenior Clinical Data Manager Permanent Buckinghamshire/Berkshire borders competitive salary + bonus and benefits Job brief: Working for a global specialty pharmaceutical company that develops and commercializes innovative products for the eye care, neuromodulator, skin care and other specialty markets.
Senior clinical research associate (scra) turkey
Clinical Professionals-Turkey - Turkey-United KingdomContract : Permanent - Salary : £Negotiable + BenefitsSenior Clinical Research Associate (SCRA) Turkey Permanent, Fulltime Office Based An exciting opportunity to work with a global Clinical Research Organisation with established global capabilities. The company is seeking high calibre senior level Clinical Research Associates to work at an international level on multiple trials.
Clinical programmer
Battle-GBSalary : 45000The Clinical Programmer, manages and supports project deliverables and timelines. Designs, writes, validates, and maintains software to meet specifications and specifies, develops, and validates applications supporting data capture and processing Core Responsibilities 1.
Clinical programmer
Battle-GBSalary : 45000The Clinical Programmer manages and supports project deliverables and timelines. They design, write, validate and maintains software to meet project specifications. They also specify, develops and validate applications supporting data capture and processing Core Responsibilities 1.
Senior clinical data associate
Battle-GBSalary : 50000Senior Clinical Data Associate Location UK, Battle Job ID 8080 Area of Interest Global Client Services Job Type Full-Time Regular Education Required Not Indicated Experience Required Not Applicable Relocation Provided.
Clinical biostatistician
South of England-United KingdomContract : PermanentOur client, a leading Clinical Research Organisation are looking for a talented Statistician to join our Biostatistics and Programming team. Responsibilities; - Your role will be to support the lead statistician or lead programmer on projects, by providing statistical support for data summaries and analyses.
Clinical imaging associate
CK Group (Science, Clinical & IT)-Middlesex-United KingdomContract : PermanentClinical Imaging Associate Our client a global drug research and development company are looking to appoint a new Clinical Imaging Associate for the team based in Uxbridge.
Clinical study specialist
CK Group (Science, Clinical & IT)-Middlesex-United KingdomContract : PermanentClinical Study Specialist - South West London Our client is a global pharmaceutical manufacturer and are currently looking to appoint the above position within the company's global imaging unit. The global imaging unit focuses on the development and application of imaging methodology to early phase clinical trials across the company's pipeline.
Senior clinical data manager
CK Group (Science, Clinical & IT)-South East-United KingdomContract : PermanentCK Clinical are currently recruiting for a Senior Clinical Data Manager to work for a leading Pharmaceutical company in the South-East, whereby you will be responsible for all Data Management activities, including data quality and the timely delivery of database locks for projects, particularly within the Oncology therapy area.
Clinical project manager - europe
CK Group (Science, Clinical & IT)-Hertfordshire-United KingdomContract : PermanentThis is a permanent position with a well established and successful Clinical Research Organisation. You will have responsibility for the planning, implementation and execution of successful clinical trials from contract transfer through to project completion.
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