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below. ProClinical Ltd. specialise in Bio/Pharmaceutical recruitment in the UK and throughout Europe... . An approved supplier to major market leading companies, ProClinical have a host of permanent and contract... , Clinical Trials Supplies and Logistics, Health Outcomes and Economicsetc. ProClinical Ltd. is acting... consultation. [URL removed] ProClinical Ltd. specialise in Bio/Pharmaceutical recruitment in the UK
Contract: Permanent
. ProClinical Ltd. specialise in Bio/Pharmaceutical recruitment in the UK and throughout Europe. An approved... supplier to major market leading companies, ProClinical have a host of permanent and contract opportunities... Trials Supplies and Logistics, Health Outcomes and Economics…etc. ProClinical Ltd. is acting
Jobs similar to "proclinical": proclinical uk manager, proclinical recruitment manager, proclinical ltd manager
Management Systems preferable. Proclinical is a specialist pharmaceutical R&D recruitment company, and any... d.----@----.uk ProClinical Ltd. specialise in Bio/Pharmaceutical recruitment in the UK and throughout Europe
Contract: Permanent
Jobs similar to "proclinical": senior proclinical, senior proclinical uk, senior proclinical regulatory, senior proclinical ltd
contact Priyam on +44 (0) 845 --- ---3 or send your CV to p.----@----.uk ProClinical Ltd. specialise in Bio/Pharmaceutical recruitment in the UK and throughout Europe. An approved supplier to major market leading... companies, ProClinical have a host of permanent and contract opportunities in Regulatory Affairs, Clinical Research, Medical Affairs, Drug Safety, Quality Assurance/Control, Clinical Trials Supplies and Logistics, Health Outcomes
or email d.----@----.uk ProClinical Ltd. specialise in Bio/Pharmaceutical recruitment in the UK and throughout Europe, on both a contract and a permanent basis. Register your CV at ----@----.uk or call 0845 338
Contract: Contract
Cambridge
Company: ProclinicalSalary: £30000 - £350000 per annum
* Main Purpose of the Role: To serve as the primary European reporting resource with responsibility for the support and management of the reporting system to provide bespoke reports and manage all documentation related to these reports. * Duties and Responsibilities: * Analyse and implement functionality of the reporting system to fulfil the reporting requirements of the EU Drug Safety and Pharmac
Buckinghamshire
Company: ProclinicalSalary: £400 - £420 per week
Clinical Trials Assistant/ Clinical Trials Administrator A very good opportunity has arisen for a CTA to join a reputable pharmaceutical company in the UK. The ideal Candidate must be able to demonstrate that they can fulfil the responsibilities and competencies listed below Tasks and responsibilities * Prepare and maintain accurate and up to date in-house trial related files (CAF) according to re
Regulatory Conformance Officer & Regualtory Associate, Hampshire, 8 Months Working on site within a major top 20 Pharmaceutical company, this role involves working within a team of seven Regulatory Affairs professionals and reporting directly to the Manager. This position has come about as a result of increased departmental workload under a restriction to new permanent headcount. The requirement i
High Wycombe
Company: ProclinicalSalary: £20 - £25 per hour
* Job Title: Drug Safety Associate * Job Type: 12 Month Contract * The Role: My client, a leading global pharmaceutical company, are looking for a Drug Safety Associate to join them on a 12 month contract basis. The job will mostly entail case processing duties such as database and literature searches, case data entry and single case unblinding. The Drug Safety Associate is required to assist with
Requirements: The ideal candidate for this role will have recent experience within Drug Safety, and would have ideally worked in this area for at least a year.
Middlesex
Company: ProclinicalSalary: £30000 - £39000 per annum + Benefits
Clinical Submissions Responsible/ Clinical Submissions specialist/ CRA/ Regulatory-Affairs Officer Our client, one of the fastest growing pharmaceutical companies in the UK with a strong pipeline of new products, is looking for someone who has relevant experience in the area of clinical submissions to work in their head office in Middlesex. Role *To review and approve labels for IMP, provide trans