Regulatory Affairs Jobs in M4 Corridor
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International Medical Information Specialist
- Salary:
- £40k - £45k pa + usual be
- Location:
- Uxbridge
- Job Type:
- Permanent
- Date Posted:
- 22-Jul-2008 09:15Add to My Shortlist
Title:International Medical Information Specialist - Stockley Park Company: My client is a bio pharmaceutical company that discovers, develops and commercializes innovative therapeutics in areas of unmet medical need. The company's mission is to advance the care of patients suffering from life-threatening diseases worldwide. Headquartered in Foster City, California, We has operations in North America, Europe and Australia. As our International...
Senior Regulatory Affairs Officer
- Salary:
- £40K
- Location:
- West London
- Job Type:
- Permanent
- Date Posted:
- 23-Jul-2008 15:22Add to My Shortlist
Senior Regulatory Affairs Officer West London £40K + Benefits A blue-chip Pharmaceutical company requires a Senior Regulatory Affairs Officer to co-ordinate and manage the preparation, submission and follow up of regulatory applications in the UK/Ireland in line with national/corporate strategies under the direction of the Regulatory Affairs Manager. To ensure that all work meets company quality standards and complies with...
Regulatory Affairs Director R&D (Oncology)
- Salary:
- Great Salary & Benefits
- Location:
- London, West London, East, Central London
- Job Type:
- Any
- Date Posted:
- 23-Jul-2008 00:00Add to My Shortlist
A fantastic opportunity has risen for a Regulatory Affairs professional to work for our TOP 20 Global Pharmaceutical Company. The company are based in Central London and have a broad spectrum of products and Specialisms. They have a very exciting pipeline as well as a number of projects in late stages of development. Main purpose of the job: To focus...
Medical Writer
- Salary:
- N/A
- Location:
- Uxbridge
- Job Type:
- Permanent
- Date Posted:
- 25-Jul-2008 00:00Add to My Shortlist
Do you want more from your medical writing career? At PAREXEL, our Medical Writing team use their writing skills for more than just writing clinical study reports. We work on varied document types including patient information and informed consent forms, protocols, pharmacovigilance documents such as PSURs and ASRs, and regulatory submission documents such as clinical overviews. We are looking for...
Medical Writer
- Salary:
- N/A
- Location:
- Uxbridge
- Job Type:
- Permanent
- Date Posted:
- 25-Jul-2008 00:00Add to My Shortlist
Do you want more from your medical writing career? At PAREXEL, our Medical Writing team use their writing skills for more than just writing clinical study reports. We work on varied document types including patient information and informed consent forms, protocols, pharmacovigilance documents such as PSURs and ASRs, and regulatory submission documents such as clinical overviews. We are looking for...
Medical Writer -Middlesex
- Salary:
- Great Salary & Benefits
- Location:
- Middlesex, West London, London
- Job Type:
- Permanent
- Date Posted:
- 24-Jul-2008 00:00Add to My Shortlist
Medical Communications Scientist / Medical Scientific Writer - Office Based - West London / Middlesex Company Summary A fantastic opportunity to work as a office-based Medical Writer, in West London / Middlesex for a world leader in the field of biotechnology. The role presents the opportunity to work in a very supportive environment, with excellent access to training, in a...
Regulatory Affairs Associate Specialising in Compliance (GCP)
- Salary:
- Competitive
- Location:
- Berkshire, Surrey, West Sussex, Middlesex, West London, South East London, Hampshire
- Job Type:
- Permanent
- Date Posted:
- 24-Jul-2008 00:00Add to My Shortlist
A TOP biotechnology company based in Surrey, are looking to recruit a Regulatory Affairs Associate within GCP. If you have 2-5 years of relevant pharmaceutical industry experience within either regulatory compliance or direct quality assurance experience then this should be your next career move! Purpose: This individual will assist in all aspects of clinical compliance and QA activities, including documentation...
Regulatory Affairs Associate Specialising in Compliance (GCP)
- Salary:
- Competitive
- Location:
- Berkshire, Surrey, West Sussex, Middlesex, West London, South East London, Hampshire
- Job Type:
- Permanent
- Date Posted:
- 24-Jul-2008 00:00Add to My Shortlist
A TOP biotechnology company based in Surrey, are looking to recruit a Regulatory Affairs Associate within GCP. If you have 2-5 years of relevant pharmaceutical industry experience within either regulatory compliance or direct quality assurance experience then this should be your next career move! Purpose: This individual will assist in all aspects of clinical compliance and QA activities, including documentation...
Medical Devices - QA / Regulatory Officer Jobs - Berkshire
- Salary:
- £20,000-25,000 pa
- Location:
- Berkshire, Reading, Bracknell, Maidenhead, Newbury, Windsor, Wokingham, Abingdon
- Job Type:
- Permanent
- Date Posted:
- 18-Jul-2008 09:59Add to My Shortlist
Flame Pharma Medical Devices - QA / Regulatory Officer Job - Berkshire: Job Summary Flame Pharma are excited to be working alongside a leader in the worldwide Orthopaedic market who are also one of the world's largest medical device companies. Our client pride themselves on delivering results through a wide range of capabilities including joint replacements, trauma, spine and micro...
Medical Information Scientist
- Salary:
- £30-35 p hour
- Location:
- Newbury
- Job Type:
- Contract
- Date Posted:
- 22-Jul-2008 00:00Add to My Shortlist
Title:Medical Information Scientist - Newbury - 3mth contract Company: My client has a goal to become a leading market position in each of its specialist fields. With its distinctive expertise, the company engages in research on new drugs which, as innovative therapies, make an essential contribution toward improving people's quality of life. Our outstanding research activities, together with our highly...
Regulatory Submissions / Clinical Study Start Up Manager
- Salary:
- c £60k neg
- Location:
- Hampshire, Surrey, Basingstoke
- Job Type:
- Permanent
- Date Posted:
- 19-Jul-2008 00:00Add to My Shortlist
Regulatory Submissions / Clinical Study Start up Manager is required for a global CRO Your responsibilities will include:- ·Coordinate and oversee the study start-up activities at project start-up and throughout the study. This includes maintaining start-up timelines. ·Maintaining ongoing Sponsor contact for start-up issues by serving as the primary contact for the Sponsor and project team members. ·Independently interact with...
Director, Regulatory Affairs
- Salary:
- £60-70k
- Location:
- Marlow, Buckinghamshire
- Job Type:
- Permanent
- Date Posted:
- 20-Jul-2008 00:00Add to My Shortlist
Job Summary: You will be working for a leading full service CRO, with broad therapeutic area expertise. You will be reporting directly to the Senior Director, Regulatory Affairs. You will provide effective management, guidance and direction and actively promote the development and best interests of the Company Requirements: Role: * You will deliver effective management, guidance and direction to assigned...
Senior Medical Writer
- Salary:
- on application
- Location:
- Oxford, Oxfordshire, South East, Abingdon, Didcot, Swindon, Witney
- Job Type:
- Permanent
- Date Posted:
- 22-Jul-2008 00:00Add to My Shortlist
A successful Oxford-based medical education agency is looking for a senior medical writer to join their small but dedicated editorial team. The senior writer will work on selected accounts providing medical writing and editing services to the company's pharmaceutical clients, working on anything from clinical papers to PowerPoint slide presentations, completing each to deadline and budget. The agency is currently...
Regulatory Affairs Manager
- Salary:
- Negotiable
- Location:
- Slough
- Job Type:
- Permanent
- Date Posted:
- 19-Jul-2008 00:00Add to My Shortlist
Our client, a leading Clinical Research Organisation is offering a fantastic opportunity for a Regulatory Affairs Manager to join their ever growing office based in Slough. The main responsibilities of the Regulatory Affairs Manager will include providing regulatory affairs advice and support for all projects, assist with the management of regulatory affairs and technical writing services within the company, Provides...
Regulatory Affairs Manager
- Salary:
- Negotiable
- Location:
- Maidenhead, Berkshire, Uk
- Job Type:
- Any
- Date Posted:
- 23-Jul-2008 00:00Add to My Shortlist
Come and speak with i3 directly about the direction of your regulatory affairs career and find how we can give you the international opening your experience deserves. i3 Research, a United Health Group Company, is a full-service, global clinical research organization therapeutically focused on: central nervous system, oncology, respiratory and infectious diseases, endocrinology and metabolic diseases, and cardiology. i3 brings...
Featured Jobs
Regulatory Submissions / Clinical Study Start Up Manager
- c £60k neg
- Hampshire, Surrey, Basingstoke ...
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