Regulatory Affairs Jobs in M4 Corridor

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Medical Adviser UK, Respiratory

*THIS IS AN OUTSTANDING CAREER OPPORTUNITY FOR EXPERIENCED PHARMACEUTICAL PROFESSIONAL OR A MEDIC WITH IN DEPTH KNOWLEDGE AND INTEREST IN RESPIRATORY. THE HIRING COMPANY IS A LEADING PLAYER IN THE RESPIRATORY AND OTHER THERAPEUTIC AREAS AND THE INCUMBENT WOULD BE EXPOSED TO THE RANGE OF INTERNAL STAKEHOLDERS AND EXTERNAL CUSTOMERS RELATED TO THE ASSIGNED PRODUCTS. *PROVIDE MEDICAL REVIEW AND APPROVAL...

Salary:
competetive base and flexible benefits
Location:
Maidenhead
Date Posted:
20-Jan-2017
Job Type:
Permanent

Regulatory Affairs Manager - Medical Devices

Regulatory Affairs Manager - Medical Devices Cardiff, Wales - 50,000 - 65,000 An opportunity to become a Regulatory Affairs Manager has become available at a leading medical device company. Upon successful application, you will be based in either Wales or Northern Ireland. Responsibility for proactively ensuring regulatory compliance across the group. Reporting directly to the Director responsible for working closely...

Salary:
50,000 - 65,000
Location:
Cardiff
Date Posted:
20-Jan-2017
Job Type:
Permanent

Regulatory Affairs Coordinator

Oliver Care is recruiting for a Regulatory Affairs Co-ordinator to join a company in the pharmaceutical industry at their site based in Berkshire on a contract basis. This is an excellent opportunity to join a pharmaceutical company developing high quality products across the world, offering a competitive salary and bonus. The main purpose of the role will be: -To support...

Salary:
26000 to 27000
Location:
Bracknell
Date Posted:
20-Jan-2017
Job Type:
Contract/Temp

Project Manager - Medical Devices - Technical Specialist

Job Title: Project Manager - Medical Devices Salary : 50,000 - 70,000 + benefits Possibly part time considered Territory: South Central .................................................................................................................................................... The Role: I have a rare opportunity to join a well funded early stage innovative medical device company. Specialising in implantable and wearable devices use wireless, battery less technology capable of capturing and analysing biometric data in real-time....

Salary:
50,000 - 70,000
Location:
Southampton, Portsmouth, Winchester, Guildford, Basingstoke, Reading
Date Posted:
19-Jan-2017
Job Type:
Permanent

Global Quality and Regulatory Affairs Manager

Our client is a private family owned global company who specialise in medical devices. They are seeking a Global Quality and Regulatory Affairs Manager to join their team. This is a dual role so you will be in charge of the entire quality and regulatory affairs process. You will have extensive experience working in a similar role within the medical...

Salary:
Up to 60k + Bonus
Location:
Bracknell
Date Posted:
19-Jan-2017
Job Type:
Permanent

Sr SSU & Regulatory Specialist (United Kingdom)

As a member of our Study Start Up team you will traverse all therapeutic areas and phases, providing your expertise at this vital period of time in the study. This expertise at this critical time has resulted in the average study start up time four weeks faster than industry standard. We are currently looking to strengthen our Ethics and Regulatory...

Salary:
Negotiable
Location:
Camberley
Date Posted:
20-Jan-2017
Job Type:
Permanent

Manager, Regulatory Records - Study Start Up (United Kingdom)

Do you want to be a part of a global top 10 CRO? INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world's pharmaceutical, biotech and medical device industries. We do this across six continents. We believe that therapeutic and operational experience forms the foundation for taking...

Salary:
Negotiable
Location:
Camberley
Date Posted:
21-Jan-2017
Job Type:
Permanent

Regulatory Compliance Reviewer - Consumer Health and OTC products

Regulatory Compliance Reviewer - Consumer Health and OTC products Start: February 2017 Duration: 6 months' initial period As part of a long-standing working partnership with one of our most valued clients, we are currently recruiting for a number of Regulatory Compliance Reviewers for our Maidenhead office. You would be joining a burgeoning team of enthusiastic and dynamic regulatory affairs professionals, ...

Salary:
Competitive
Location:
Maidenhead
Date Posted:
21-Jan-2017
Job Type:
Contract/Interim

Regulatory CMC Writer

Regulatory CMC Writer - Biopharmaceutical/Vaccine products Start: Immediate Duration: 6 months initial period, further 12-18 month extension 2017 is starting out on a very positive note for Genpact Pharmalink - we are kicking January off with a major new CMC project for one of largest pharmaceutical companies in the world. We are building the new team across our offices on...

Salary:
Competitive
Location:
Maidenhead
Date Posted:
21-Jan-2017
Job Type:
Contract/Interim

Senior Regulatory Affairs Associate

Senior Regulatory Affairs Associate We are looking for an experienced Regulatory Affairs Associate with a strong background in Clinical Research who is passionate about drug development and are seeking a challenging and rewarding career in a commercially focused role. - You will be expected to take responsibility for managing clinical trial applications of new and established pharmaceuticals performed, ensuring that...

Salary:
40, 000-55, 000
Location:
Slough, London
Date Posted:
19-Jan-2017
Job Type:
Permanent

SSU & Regulatory Specialist II (United Kingdom)

Summary: Performs assigned activities within the country that lead to start-up of investigative sites in all phases of clinical trials. Responsible for providing delivery and expertise in one or more of the following functional areas: investigator site contracts, ethics and regulatory submissions, and review and finalization of essential documents required for site initiation. Ensures local activities are undertaken in accordance...

Salary:
Negotiable
Location:
Camberley
Date Posted:
20-Jan-2017
Job Type:
Permanent
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SSU & Regulatory Specialist II (United Kingdom)

Summary: Performs assigned activities within the country that lead to start-up of investigative sites in all phases of clinical trials. Responsible for providing delivery and expertise in one or more of the following functional areas: investigator site contracts, ethics and regulatory submissions, and review and finalization of essential documents required for site initiation. Ensures local activities are undertaken in accordance...

Salary:
Negotiable
Location:
Camberley
Date Posted:
20-Jan-2017
Job Type:
Permanent

Regulatory Clinical Trial Submissions Manager

My Client a Global Pharmaceutical Company has opened a new vacancy within their Regulatory team and are looking to recruit a Regulatory Affairs Manager on an initial 12 Month contract basis to be based at there offices in Buckinghamshire. The role will be involved with day to day Regulatory Activities related to Regulatory filings to support Global Regulatory strategies within...

Salary:
1 p hour
Location:
High Wycombe
Date Posted:
16-Jan-2017
Job Type:
Temporary/Seasonal

SSU & Regulatory Specialist I (12 Month Contract)

We are currently looking to strengthen our Ethics and Regulatory department in the UK and are seeking an experienced SSU & Regulatory Specialist I to be based in our office in Camberley or Edinburgh or other European locations. A brief summary of duties you will be involved in as a Site Start up Specialist I : * Reviewing essential document...

Salary:
Negotiable
Location:
Camberley, Edinburgh
Date Posted:
20-Jan-2017
Job Type:
Permanent

SSU & Regulatory Specialist I (12 month Contract)

We are currently looking to strengthen our Ethics and Regulatory department in the UK and are seeking an experienced SSU & Regulatory Specialist I to be based in our office in Camberley or Edinburgh or other European locations. A brief summary of duties you will be involved in as a Site Start up Specialist I : * Reviewing essential document...

Salary:
Negotiable
Location:
Camberley, Edinburgh
Date Posted:
20-Jan-2017
Job Type:
Permanent

Regulatory Affairs Officer- Pharmaceutical/ Reg Affairs

Role Summary An exciting opportunity has arisen to join our Regulatory Affairs team, based in Maidenhead, Berkshire. Responsibilities Prepare and submit applications of reliable quality in a timely manner to MHRA (UK) via National Procedure. These include new licence applications, variations (including grouping and work sharing), renewals, artwork changes, RFIs, updates and any other relevant applications or notifications. Work with...

Salary:
25-40k
Location:
Maidenhead
Date Posted:
20-Jan-2017
Job Type:
Permanent

Senior Regulatory Manager Emerging Markets

Senior Regulatory Affairs Manager, Emerging markets, APAC, LATAM, CEER, Middle East Your new company This leading biotech is looking to strengthen their Regulatory Affairs team with the appointment of a Senior Regulatory Affairs Manager on a 6 month contract within their Emerging Markets team with scope for contract extension Your new role This is an interesting contract as you will...

Salary:
60.00 - 70.00 p hour
Location:
Maidenhead
Date Posted:
16-Jan-2017
Job Type:
Contract/Interim

Regulatory Affairs Manager Emerging Markets

Regulatory Affairs Manager, LATAM, APAC, Middle East, CEER, emerging markets Your new company This leading biotech is looking to strengthen their Regulatory Affairs team with the appointment of a Regulatory Affairs Manager on a 6 month contract within their Emerging Markets team with scope for contract extension Your new role This is an interesting contract as you will be working...

Salary:
50.00 - 60.00 p hour
Location:
Maidenhead
Date Posted:
16-Jan-2017
Job Type:
Contract/Interim

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:
21-Jan-2017
Job Type:
Permanent

SCRA - Small CRO - CNS - UK - 37-42, 000 - Homebased

SCRA - Senior Clinical Research Associate - Small CRO - CNS - UK - 37-42,000 - Homebased Upsilon Global are currently seeking a Senior CRA for a small Scottish CRO specialising in the delivery of CNS focused clinical trials. Our client is looking for an experienced CRA to work as part of a small clinical team and monitor key sites...

Salary:
37-42, 000
Location:
Home Based
Date Posted:
19-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

Medical Writer II

Medical Writer II, Global CRO Medical Writer II required for a Top Clinical Research Organisation. You will be responsible for a variety of clinical documents for a wide range of both international and local sponsors across all therapeutic areas. This role would suit someone with some MW experience looking to advance their career. The focus of the role will be...

Salary:
0.00 pa
Location:
Berkshire, Home Based
Date Posted:
20-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:
20-Jan-2017
Job Type:
Permanent
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