Regulatory Affairs Jobs in Cambridge

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Process Improvement Facilitator - ROW

A leading US biopharmaceutical organisation with a solid commercial portfolio of life-saving drugs within a number of therapy areas have a new Process Improvement Facilitator job opportunity at their offices in Cambridge, UK. The company has a growing pipeline of investigational drugs and approximately 5,000 employees in offices across four continents. This is a contract position. Role and Responsibilities: *...

Salary:
450 - 550 per day
Location:
Cambridge
Date Posted:
16-Jan-2017
Job Type:
Contract/Interim

Process Improvement Facilitator - ROW

An opportunity has arisen for a Process Improvement Facilitator to join a leading pharmaceutical company on an 18 month contract, within their Regulatory Affairs Team. Job Role and Responsibilities: * The Process Improvement Facilitator is responsible for project management for Rest Of World (ROW) 3 year road map initiative * Organises, facilitates and participates in meetings with the regulatory teams...

Salary:
65 - 75 per hour
Location:
Cambridge
Date Posted:
12-Jan-2017
Job Type:
Contract/Interim

CMC Pharma Development Director -Cambridgeshire

CMC Pharma Development Director -Cambridgeshire I am currently working with an exciting company, who are looking for a CMC Director to lead late stage development. Working within pharmaceutical development, you should have a strong background within Formulation, Analytics and CMC all within small molecules. This is a position based in Cambridgeshire, offering you the chance to really be responsible for...

Salary:
Neg
Location:
Cambridge
Date Posted:
12-Jan-2017
Job Type:
Permanent

Medical Writer (Regulatory)

As part of our on-going growth, we are currently recruiting for a Senior Medical Writer to join our rapidly expanding team of over 90 regulatory writers based in Europe, North American and Asia Pacific. The Phase II-IV Medical Writing group, which is part of the Biostatistics Department, includes Writers who prepare documents in support of clinical trials and who assist...

Salary:
competitive
Location:
Cambridge
Date Posted:
17-Jan-2017
Job Type:
Permanent

Senior Regulatory Associate, Great Salary - Biopharma

Senior Regulatory Associate, Hepatology. Work for one of the Top Biopharma's in the UK. Development, Registrations and Established Products - Centralised Procedure. This is for one of theindustry's most successful companies!! This role is within the Hepatology Portfolio. Ideally, you will have good working knowledge and experience of the full Regulatory pipeline: CTA's, CTD/Dossiers for MAA's; National Submissions and Centralised...

Salary:
44,000 to 54,000, bonus and leading benefits
Location:
Cambridge, Essex, Hertfordshire, Suffolk, Norfolk
Date Posted:
12-Jan-2017
Job Type:
Permanent

Technical Specialist, Science and Technology

For our Production and Development site we are currently looking for a home office based Technical Specialist, Science and Technology in Germany The Technical Specialist, Science and Technology, will support and execute assigned sections of Catalent Science and Technology strategy for the region, leveraging the internal scientific community and external collaborations to drive Catalent's brand for innovation and advanced drug...

Salary:
TBD
Location:
Germany, Home Based
Date Posted:
14-Jan-2017
Job Type:
Permanent

Executive Director, Regulatory Consultant PPD (EMEA wide)

We are seeking an Executive Director to join our global PPD Consulting group in the EMEA region as Clinical Regulatory Consultant. This is primarily for the therapeutic areas of gene therapy and rare disease. The role can be office or home based in any of the European countries where PPD has an office. PPD are seeking a candidate based in...

Salary:
competitive package
Location:
Home Based
Date Posted:
17-Jan-2017
Job Type:
Permanent

Senior Specialist or Manager - Global Regulatory Affairs - UK

Worldwide Clinical Trials (WCT) currently have a permanent vacancy to support activities due to new projects. Experience in Global submission is required.Must have multi countries experience. Company: Worldwide Clinical Trials Ltd Location: Home based UK Reference: Manager, Regulatory Affairs Type: Permanent, Salary (): On Application (Highly competitive) Benefits: Bonus + benefits Job summary: Exciting opportunity within a leader global CRO...

Salary:
Competative
Location:
Home Based
Date Posted:
13-Jan-2017
Job Type:
Permanent
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