Science Jobs

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CMC Associate - Pharmaceutical Sciences.

Salary:
Good Package
Location:
Hampshire
Job Type:
Permanent
Date Posted:
02-Feb-2012 14:05Add to My Shortlist

CMC Associate required by a forward thinking pharmaceutical company located in Hampshire. New Posting Role This new permanent role at our pharmaceutical client is to support CMC submission compliance within the Pharmaceutical Sciences division. The ideal candidate will be familiar with CMC submissions, compliance issues and be an expert in Documentum. This role requires excellent problem solving ability and the...


Service Support Engineer - Science

Salary:
£27,000 - £32,000
Location:
Field Based, London
Job Type:
Permanent
Date Posted:
02-Feb-2012 16:01Add to My Shortlist

Service Support Engineer / Commissioning Engineer - Scientific / Instrumentation / Medical Devices Field based - Covering London area £27,000 - £32,000 per annum plus company vehicle & competitive employee benefits Our client is responsible for the world's most comprehensive range of scientific instrumentation available under one brand - a brand synonymous with excellence, innovation and quality for 50 years....


Medical Science Liaison Manager - East Anglia

Salary:
£44 - 50k
Location:
East Anglia
Job Type:
Permanent
Date Posted:
03-Feb-2012 13:48Add to My Shortlist

Contract Our client, a successful and growing family-owned pharmaceutical organisation is passionate about being the preferred partner in pain management. In recent years, they have made considerable investments in research and development and are intensively searching for new ways of improving pain relief and reducing side-effects. They have recently launched a new and exciting product for the treatment of chronic...


Senior Clinical Program Manager

Salary:
£50k - £62k pa + 14% Bonus + 25/days holiday
Location:
Crawley
Job Type:
Permanent
Date Posted:
01-Feb-2012 12:31Add to My Shortlist

We have an exciting opportunity for an office based Senior Clinical Program Manager for our large global pharmaceutical client. SUMMARY Accountable for all aspects of assigned clinical trials (Phase II through lifecycle management) including leading Clinical Trial Team(s). Lead complex trials or programs or manage trials within an alliance partnership. Responsible for development of reports including providing training opportunities and...


Regulatory Labelling Contractor

Salary:
£50 - £80 p hour
Location:
Uxbridge
Job Type:
Contract/Interim
Date Posted:
30-Jan-2012 15:36Add to My Shortlist

Job title: Regulatory Labelling Contractor Job type: 6 month contract + extensions Location: Uxbridge, Greater London Salary: £50 to £80 / hour A Regulatory Affairs Labelling Specialist with experience of prescribing and patient information is required by a leading Pharmaceutical company based in the Greater London area The ideal candidate will be responsible for managing and developing EU labelling documents, ...


CC / CRA Italy

Salary:
€30, 000-€40, 000
Location:
Milan
Job Type:
Permanent
Date Posted:
01-Feb-2012 00:00Add to My Shortlist

World-Leading CRO in quest of a driven and determined CRA's to become a member of a well organised team within a fantastic work environment which offers the ideal candidate the chance to work on impressive international trials and fantastic career development. * Assist in managing large scale clinical trial projects or function as project manager for small scale projects, ensuring...


Clinical Project Manager (Phase IV) - International CRO - Italy

Salary:
€55
Location:
Italy
Job Type:
Permanent
Date Posted:
31-Jan-2012 00:00Add to My Shortlist

A superb opportunity exists within one of the world's leading CRO's for a Clinical Project Manager with strong late phase (Phase IIIb / Phase IV) experience. This company are paying a salary of over €55k with bonus and health plan, and with the chance to be based anywhere in Italy, this really is an excellent opportunity for candidates looking to...


CRA II - Milan, Italy

Salary:
28,000.00-33,000.00 GBP
Location:
Italy
Job Type:
Permanent
Date Posted:
03-Feb-2012 00:00Add to My Shortlist

Want to develop your career, working for a dynamic, diverse and professional organisation? Look no further! We are currently seeking a Clinical Research Associate II to be office based in Milan ( Italy). You will perform the clinical monitoring aspect of designated projects in accordance with applicable SOPs and regulations. As CRA II, you will be responsible for performing clinical...


Prinicipal Data Co-ordinator - Germany

Salary:
35,000.00-40,000.00 GBP
Location:
Germany
Job Type:
Permanent
Date Posted:
01-Feb-2012 00:00Add to My Shortlist

PRINCIPAL DATA CO-ORDINATOR - GERMANY (SALARY: 35,000.00-40,000.00 GBP) (BASED IN: GERMANY) This major international Clinical Research Organisation provides a comprehensive range of Clinical Research services to the pharmaceutical and biotechnology industries. Primary responsibility is to serve as a member of the project team with the lead responsibility for reviewing CRFs, data listings, and databases to ensure that all captured data...


Commercial Manager - London

Salary:
Up to £50k
Location:
London
Job Type:
Permanent
Date Posted:
03-Feb-2012 12:27Add to My Shortlist

Permanent Headcount Job Purpose and Background Our client's industry brings life-saving and life-enhancing medicines to patients and represents innovative research-based biopharmaceutical companies leading an exciting new era of biosciences in the UK. This role is to provide comprehensive support on all matters relating to pricing, the PPRS and the next scheme in 2014, including project management and logistics support of...


Medical/ Regulatory Communications Scientist

Salary:
£200 - £280 p/day
Location:
Cheshire
Job Type:
Contract/Interim
Date Posted:
02-Feb-2012 00:00Add to My Shortlist

Align and build clinical-regulatory information across the product life cycle so that project strategy is consistently implemented across all study designs, and clear and supportable messages are communicated to internal customers (product teams, governance bodies) and external customers (regulatory authorities, payers, physicians and patients). Information creation and alignment at the Document, Programme and Strategy level. Integration of strategic elements into...


CMC Senior Regulatory Executive

Salary:
£50 - £70 p hour
Location:
South East England
Job Type:
Contract/Interim
Date Posted:
03-Feb-2012 16:47Add to My Shortlist

Job Title : CMC Senior Regulatory Executive Location : Middlesex , South East England Contract Rate : £50-£70 per hour depending on experience Contract Length : 12 Months + possible extensions A Senior Regulatory CMC specialist with strong documentation experience is required by a leading Pharmaceutical company based in the Greater London area. The ideal candidate will be responsible for...


Senior Medical Information Executive - Bucks

Salary:
Circa £40k
Location:
Buckinghamshire
Job Type:
Contract/Interim
Date Posted:
01-Feb-2012 00:00Add to My Shortlist

Contract Our client is an established leader in the field of Dermatology and attracts and retains well-educated, motivated and results-oriented people who are eager to make a contribution to the development of the company. They are currently looking for a Senior Medical Information Executive. Job Puropse 1. With Head of Medical Information and Pharmacovigilance ensure the smooth day to day...


Clinical Project Manager - Dusseldorf

Salary:
€85,000 - 100,000
Location:
Dusseldorf
Job Type:
Permanent
Date Posted:
04-Feb-2012 00:00Add to My Shortlist

Clinical Project Manager - Dusseldorf Package €85,000 - 100,000 If you are a Clinical Project Manager or Lead CRA with at least 3 years of European Clinical Experience, this could be your next position as Clinical Project Manager. The Clinical Project Manager would head up the Clinical Team and the Clinical Project, being responsible for line management, budgetary control and...


Contract Senior Study Manager, Phase III/ IV

Salary:
£300 - £400 p/day
Location:
Marlow
Job Type:
Contract/Interim
Date Posted:
31-Jan-2012 19:06Add to My Shortlist

To be considered for this role you must have delivered international clinical studies, ideally in Phase III/IV, managed from a European hub. This is an office based full time post with periodic travel, studies are outsourced after protocol design and vendor liaison and oversight from planning reporting and close association with brand teams form a significant part of this role....


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