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Earth/Environmental Sciences Jobs in Middlesex

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Regulatory Affairs Labelling Consultant

Salary:
£30 - £60 p hour
Location:
West London
Job Type:
Contract/Interim
Date Posted:
24-May-2012 00:00Add to My Shortlist

A Global Pharmaceutical company are presently looking to bring on a Regulatory Labelling Consultant to be based in the UK West London Office, on a contract basis. This role involves managing the creation, review, approval and implementation of Global Data Sheets (GDSs) and Global Patient Leaflet. To provide support for labelling submissions for MRP/DCP. Role: - Management of the development... questions. - Participation in other projects and activities as required. - Management of the development and maintenance of EU CP and MR/DCP labelling documents throughout the product lifecycle. Experience: - Life sciences degree and relevant experience. - Demonstrated understanding of labelling regulations for medicinal products. - Pharmaceutical labelling experience in Regulatory Affairs, including labelling preparation, leading/participating in labelling review meetings, and labelling submissions. - Direct experience of managing labelling issues. To Apply: To apply, please click on the Apply button. Ideally, please include a short note outlining why you are interested in the role and why you think you are suitable. In...

Oncology Regulatory Affairs Manager

Salary:
Neg
Location:
Uxbridge
Job Type:
Contract/Interim
Date Posted:
24-May-2012 17:00Add to My Shortlist

My client seeks to deliver truly innovative and life-changing drugs for their patients. Their mission is to build a major global biopharmaceutical corporation while focusing on the discovery and the development of products for the treatment of cancer and other severe, immune, inflammatory conditions. They are currently recruiting for an Oncology Regulatory Manager to work a 12 month Fixed Term... Regulatory documents in electronic and paper format. * Identify issues that will impact programs and work with regulatory colleagues to provide strategies for dealing with them. * Participate or act as EU regulatory representative on various cross-functional teams You the successful candidate will hold a degree, or equivalent, in a scientific discipline and will have extensive Phase III Oncology experience. You will also have a proven European Regulatory background, with a strong understanding of the laws, regulations and guidelines related to drug development. Strong project management skills are also required to be successful in this role. In return an excellent salary...

Regulatory Affairs Consultant - CMC

Salary:
£25 - £60 p hour
Location:
West London
Job Type:
Contract/Interim
Date Posted:
24-May-2012 00:00Add to My Shortlist

A Global Pharma company are presently looking to bring in a Regulatory Affairs Consultant and also a Senior Regulatory Affairs Consultant for their CMC group, within the EU team to be based in the UK West London Office, on a contract basis. Role: - Preparation of high quality, chemistry manufacturing and control (CMC) detailed regulatory documents using varied information sources. - Liaising...

Reg Aff Man - Labelling Great Company

Salary:
£50k - £60k pa + EXCELLENT BENEFITS
Location:
Middlesex
Job Type:
Permanent
Date Posted:
29-May-2012 15:42Add to My Shortlist

Spread your wings with an exciting opportunity to work for a fast growing Pharma company This is an exciting opportunity for a Regulatory Affairs Professional to develop their career with a reputable mid-sized pharma company who are focused on getting the best out their employees. The successful candidate will be a Reg Affairs specialist will have over 5 years experience and...

Senior Consultant RA CTA Specialist

Salary:
£40k - £60k pa + competitive benefits package
Location:
Middlesex
Job Type:
Permanent
Date Posted:
24-May-2012 21:12Add to My Shortlist

Great career development opportunity for a Consultant or Senior Consultant to join a global CRO conveniently located in Middlesex. If youre looking to broaden your CTA skills then this is a great opportunity to work with a number of world class companies throughout Europe. The ideal candidate will have CTA experience to include protocol reviews. This is a great chance for a candidate with 3-5 years experience in Regulatory Affairs to broaden their skills in a varied role. If youre looking to broaden your skills and gain career development then please call Chloé Fox at NonStop Recruitment on 0207 940 2105 or e-mail c.fox@nonstop-recruitment .com

Senior Materials Engineer

Salary:
£30, 000-£45, 000
Location:
London, Hammersmith
Job Type:
Permanent
Date Posted:
24-May-2012 00:00Add to My Shortlist

Job Title- Senior Materials Engineer Employment Type - Permanent Location - London, Hammersmith Remuneration Package- Private Healthcare, Money Purchase Pension Plan, 32 days holiday inc bank holidays Salary - £30,000-£45,000 Dependant on Experience About the client Our client is the leading consultancy delivering planning, design and management services for developing infrastructure and buildings worldwide. Their Asset Management Group is based...

Senior GCP Auditor

Salary:
Up to £55,000
Location:
Berkshire, Buckinghamshire, Middlesex
Job Type:
Permanent
Date Posted:
26-May-2012 00:00Add to My Shortlist

Benefits: Up to £55,000 + Bonus + Car + Pension + Medical + Life Assurance + Parking JOB SUMMARY Opportunity to join this Global Pharmaceutical Company as their permanent Senior GCP Auditor. Through the execution of quality audits, you'll provide assurance of the level of GCP and GvP Compliance throughout the organization (Global). BACKGROUND Global Headquarters for specialist Pharmaceutical Company... follow-up measures. Assess adequacy of responses to audit findings. Support functional areas and Global QA during supplier approval process. Review and revise relevant procedures as needed. Act as GCP/GvP compliance consultant for projects, GCP training, task forces, continuous improvement projects etc. Conduct periodic training QUALIFICATIONS / EXPERIENCE REQUIRED: * A scientific degree is essential / formal auditing qualification is desirable * Strong technical knowledge and experience in application of Global regulations and guidelines for GCP in Europe and the US * Understanding of medical devices (ISO) regulations is desirable. * Experience in performance of a variety of audits including but not...

Medical Writing Manager

Salary:
up to £240 per day
Location:
Stockley Park, Uxbridge, Uk,
Job Type:
Contract/Interim
Date Posted:
25-May-2012 12:55Add to My Shortlist

Start Date : ASAP Duration: 6 month Contract Rate: GBP240 per day Location: Stockley Park, Uxbridge, UK. Basic qualifications: Bachelor of Science * Has good theoretical understanding of research principles within a particular area of medicine or science. * Demonstrates solid scientific technical expertise and the ability to independently apply new knowledge and operational processes accordingly. * Possesses excellent writing skills * Possesses excellent computer skills, literacy, technical and statistical skills. * Understands and is able to independently analyse/critique/assess trends and patterns in both text and statistical data and communicate findings clearly...

Associate, Clinical Trial Supplies

Salary:
On Application
Location:
Hertfordshire, London, Middlesex, Buckinghamshire
Job Type:
Permanent
Date Posted:
26-May-2012 00:00Add to My Shortlist

JOB SUMMARY: To coordinate, under supervisory direction, IMP packaging, labeling, distribution and accountability activities contributing to the on-time delivery of quality-driven clinical supplies. To collaborate with clinical supply team colleagues and external vendors in the creation of value within the overall clinical development process. PRIMARY DUTIES: Main duties/responsibilities: * Coordinate, under supervisory direction, IMP packaging and labeling activities * Work... at AXESS Limited on 020 8560 2300. To apply, please send your CV to jobs@axess.co.uk quoting reference 5184 . Only candidates with EU work authorisation will be considered. ABOUT AXESS: AXESS has been operating since 1990 We are a recruitment business dedicated to the pharmaceutical industry, specialising in Medical Affairs, Regulatory Affairs & Clinical Development We match professional candidates to the best permanent, contract and interim roles in the market Visit us at [URL removed]

Scientific Affairs Manager (EU/ Dermatology)

Salary:
On Application
Location:
Berkshire, Buckinghamshire, London, Middlesex
Job Type:
Permanent
Date Posted:
26-May-2012 00:00Add to My Shortlist

BACKGROUND Our Client is one of the world's leading research-based pharmaceutical companies that combines both individual talent and technical resources to create a platform for the delivery for strong growth in a rapidly changing healthcare market. Their mission is to improve the quality of human life by enabling people to do more, feel better and live longer. PRIMARY DUTIES Medical scientific input into promotional materials ensuring they are an ethical, fair and balanced representation of the known body of information and comply with all relevant guidelines, codes and laws. * Supporting the responsible medical adviser to achieve robust and timely collaborative clinical research projects. * Medical scientific input into the creation...

Associate Director Clinical Operations Neuroscience

Salary:
On Application
Location:
Cambridgeshire, Essex, Hertfordshire, London, Middlesex
Job Type:
Permanent
Date Posted:
24-May-2012 09:14Add to My Shortlist

JOB SUMMARY: Rare opportunity for a Senior Project Manager/Programme Manager looking to progress into an Associate Director role within a top tier Pharma Company. This role will involve both strategic and scientific leadership for assigned studies and/or have overall Clinical Operations responsibility for a specified compound within the Neuroscience portfolio. May also have responsibility for direct reports, including hiring and development. BACKGROUND: Top Tier Pharmaceutical company based in Hertfordshire PRIMARY DUTIES: * Ensuring that Clinical Operations activities for the assigned projects proceed...

Medical Writing Scientist (Secondment)

Salary:
On Application
Location:
Berkshire, Buckinghamshire, Middlesex, London, Hampshire
Job Type:
Contract/Interim
Date Posted:
26-May-2012 00:00Add to My Shortlist

JOB SUMMARY: 9 month maternity contract. This secondment will offer the individual an opportunity to focus on the medical writing needed in late stage clinical development projects. The individual will gain exposure to and interact with members of global Clinical Project teams, including Clinical, Contract Research Organizations, Global Regulatory Affairs, Safety and Statistics colleagues. BACKGROUND: Top Tier Global Pharmaceutical Company PRIMARY DUTIES: * Support the preparation of critical regulatory documents for US, EU and Emerging Markets/Asia Pacific including clinical summaries of efficacy and safety, clinical overviews, clinical study reports, investigators brochures, briefing documents, for regulatory meetings, clinical modules of INDs...

Medical Affairs Manager (Acquired Bleeding)

Salary:
On Application
Location:
Surrey, London, East Sussex, Kent, Middlesex, West Sussex
Job Type:
Permanent
Date Posted:
26-May-2012 00:00Add to My Shortlist

Benefits: Standard (including car and bonus) JOB SUMMARY This is an exciting opportunity for an experienced Medical Information / Medical Scientific Affairs specialist looking to further their career within Medical affairs. You will be responsible for handling UK Medical Information queries, ZINC review and providing product specific and SOP training internally and externally as required. BACKGROUND Our client is a global leader in the Biotherapeutics industry. They research, develop, manufacture and...

Regulatory Documentation Scientist

Salary:
On Application
Location:
Essex, Hertfordshire, London, Middlesex
Job Type:
Permanent
Date Posted:
24-May-2012 09:14Add to My Shortlist

JOB SUMMARY: Here is a great opportunity to combine your scientific knowledge and writing skills in an important role with one of the world's leading healthcare companies. You will be responsible for the project management and preparation of vital safety regulatory reports for innovative products and part of a global team driving the development of our clients rich pipeline of new...

CMC Project Manager

Salary:
On Application
Location:
Berkshire, Buckinghamshire, London, Middlesex
Job Type:
Permanent
Date Posted:
25-May-2012 09:06Add to My Shortlist

JOB SUMMARY: Permanent position for a CMC Project Manager to work within this renowned Global Pharmaceutical Company. Responsibilities include: product registration, submissions, representing Regulatory cross functionally, coordinate affiliates and ensuring compliance across life cycle. The role has strategic elements and will see you mentor and train team members. BACKGROUND: Broad based Global Pharmaceutical Company EU HQ based in M4 /... appropriate. Ensure input from sub-team members and issue international regulatory plans as appropriate. Attendance at project teams (Brand teams, Product Workstreams, CMC Workstreams etc.) and sub-team meetings, representing EPD RA as appropriate. Prepare regulatory filings for submission to international regulatory agencies. Manage strategy for response to regulatory agency queries, ensuring scientific dossier content and consistency of scientific content and Company position across geographic areas. Coordinate assigned affiliate(s) workload planning & prioritisation and performance. Monitor actual vs. planned activities and timelines. Identify issues impacting project progression and work with manager to recommend improvements to correct or accelerate project progression Prepare and present...

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