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| Job Field | Discipline | Region | Actions |
| Regulatory And Drug Safety | Regulatory Affairs | Bedfordshire, Cambridgeshire, Essex (United Kingdom) | Details |
| The role will be responsible to develop and implement regional regulatory strategies to expedite global drug development and registration and manage the execution of regional strategy, communications and submissions. You will have expertise on regional regulatory requirements and precedence.
The ideal candidate must have significant experience of working with the Centralised procedure as well... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Regulatory Affairs | Surrey, Middlesex (United Kingdom) | Details |
| We are seeking candidates with solid regulatory management skills in R&D or product licensing. Current understanding of pharmaceutical product development in EU is essential to allow swift adaptation to in this role.
This role is a senior management role and will demand skill in negotiating with peers and managers across alldisciplines involved in making and maintaining regulatory... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Regulatory Affairs | Essex, Middlesex (United Kingdom) | Details |
| Responsibilities:
Use expertise in IE markets to provide input into product strategy for the IE region
Preparation of International Market Applications for new products
Review of post-marketing variations (labelling and CMC)
Generation of responses to agency questions. This includes:
Manage execution of product strategies for assigned MAA and variations
Interface with regional... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Regulatory Affairs | Essex, Surrey, Middlesex (United Kingdom) | Details |
| Our Client, a leading Biotech company, is currently recruiting additional Regulatory Managers. You will be responsible for developing and implementing effective regulatory strategies for assigned projects enabling the development and registration of the company's commercial product portfolio in the Middle East/Africa; Non-EU Central/Eastern Europe; Asia/Pacific and Latin America. As the lead... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Regulatory Affairs | Essex, Surrey, Middlesex (United Kingdom) | Details |
| Responsibilities:
Use expertise in IE markets to provide input into product strategy for the IE region
Preparation of International Market Applications for new products
Review of post-marketing variations (labelling and CMC)
Generation ofresponses to agency questions. This includes:
Manage execution of product strategies for assigned MAA and variations
Interface with regional regulatory,... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Regulatory Affairs | Bedfordshire, Cambridgeshire, Essex (United Kingdom) | Details |
| The role will be responsible to develop and implement regional regulatory strategies to expedite global drug development and registration and manage the execution of regional strategy, communications and submissions. You will have expertise on regional regulatory requirements and precedence.
The ideal candidate must have significant experience of working with the Centralised procedure as well... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Regulatory Affairs | Any Location (Ukraine) | Details |
| Main Duties & Responsibilities:
- To act as a regulatory project manager for assigned clinical studies in any phase of development.
- Coordination and project management of worldwide CTA applications and CTA amendments in line with client expectations and allocated budget.
- Prepare, review and compile regulatory CTA applications, amendments, and end of trial notifications.
- Liaise... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Regulatory Affairs | Cheshire (United Kingdom) | Details |
| We are looking for a Product Safety Officer to join the regulatory affairs department of an expanding specialist chemicals company. Reporting to the Regulatory Affairs Manager, you will take responsibility for product safety and hazard communication; this involves producing MSDSs, labels and transport documentation. Experience in producing MSDSs is essential.... [Full Details] |
| Salary: 18000 - 22000 £ |
| Regulatory And Drug Safety | Regulatory Affairs | Cheshire (United Kingdom) | Details |
| An opportunity for a Technical Administrator to join the regulatory affairs department of a specialist chemicals company. Reporting to the Regulatory Affairs Manager, you will take responsibility for the production of regulatory documentation; this includes MSDSs, labels and transport documentation. Previous experience with regulatory documentation and MSDSs is essential.
Regulatory Affairs... [Full Details] |
| Salary: 18000 - 20000 £ |
| Regulatory And Drug Safety | Regulatory Affairs | Avon, Bedfordshire, Berkshire, Buckinghamshire,... | Details |
| I am currently working with a major client of mine, who are looking for a senior regulatory consultant to work in their offices just outside London.
The successful candidate will posess the following;
• Degree in a relevant life science subject or equivalent
• Considerable regulatory experience, including labelling and other safety-related regulatory activities
• A good... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Regulatory Affairs | Any Location (Hungary) | Details |
| Main Duties & Responsibilities:
- To act as a regulatory project manager for assigned clinical studies in any phase of development.
- Coordination and project management of worldwide CTA applications and CTA amendments in line with client expectations and allocated budget.
- Prepare, review and compile regulatory CTA applications, amendments, and end of trial notifications.
- Liaise... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Regulatory Affairs | Any Location (Slovakia) | Details |
| The main duties & responsibilities:
- Track of status and progress of regulatory documentation.
- Review, edit and proofread regulatory documentation.
- Assist in preparation and review of labelling and other departmental documents.
- Support local marketing by means of timely and effective communication.
- Compile under supervision regulatory documents for submission.
- Participate as... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Regulatory Affairs | Middlesex (United Kingdom) | Details |
| Our Client, one of the world's leading biotech companies, has a vacancy for a Regulatory Affairs Manager to work within the Oncology Therapeutic Area.
The Regulatory Affairs Manager will facilitate product development and global registration to achieve the desired regional labelling by developing and executing regulatory strategies and effective regulatory agency interactions.
Candidates... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Regulatory Affairs | Any Location (Austria) | Details |
| Responsibilities:
• You will be responsible for development, preparation, and submission of applications and notifications to international regulatory agencies and government bodies
• You will provide input to product development projects and changes to existing products
• You will provide input to the development of regulatory strategies and obtaining regulatory approvals from... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Regulatory Affairs | Any Location (France, Germany) | Details |
| Regulatory Affairs Specialist
LOCATION
Paris France, could be home based in France or Germany
COMPANY STATEMENT
Medical Device development company with a very strong reputation for expertise in medical device development. Although a fairly young company it is based on hiring highly experienced Medical device professionals who all bring their own experience and... [Full Details] |
| Salary: Negotiable (40000 - 45000 £) |
| Regulatory And Drug Safety | Regulatory Affairs | Any Location (United Kingdom) | Details |
| Regulatory Officer. Permanent. Berkshire. £30,000-£35,000.
A global company with a large portfolio of products are currently looking for a Regulatory Affairs Officer to join their team.
As Regulatory Officer you will be responsible for :
* Co-ordinating and undertaking the preparation of high quality license applications in order to gain approval for clinical trials and the marketing... [Full Details] |
| Salary: Negotiable (30000 - 35000 £) |
| Regulatory And Drug Safety | Regulatory Affairs | Any Location (United Kingdom) | Details |
| Regulatory Affairs Consultant- CMC. 12 month Contract. London. Salary upon application
An exciting opportunity has arisen for a Regulatory Consultant to co-ordinate and manage a Module 3 CMC exercise.
As Regulatory Consultant you will be responsible for:
* Managing team resources for regulatory in conjunction with the Module 3 Project Manager, including line management... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Regulatory Affairs | Any Location (Germany) | Details |
| Give your Regulatory Affairs Career the International experience it deserves!
i3’s Global Regulatory Affairs team provides expert regulatory support for i3’s conduct of clinical trials in 40+ countries across the globe.
Being assigned to global regulatory projects as a Regulatory Associate II you will able to coordinate the regulatory and ethics submissions for international... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Regulatory Affairs | Any Location (Russia) | Details |
| Give your Regulatory Affairs career the experience it deserves!
i3’s Global Regulatory Affairs team provides expert regulatory support for i3’s conduct of clinical trials in 40+ countries across the globe.
Assigned to global regulatory projects as a Regulatory Associate, you will coordinate the regulatory and ethics submissions for our studies in Russia.
This is a challenging and... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Regulatory Affairs | South Yorkshire (United Kingdom) | Details |
| Clinical Quality Assurance Auditor GCP GLP GCLP – CRO - £30,000+ and Excellent benefits
SUMMARY
There is now the opportunity for an experienced Quality Auditor to join this hugely successful organisation in a senior role within their UK operation. It is a strategically hands-on opportunity in their Quality assurance function and team and being the key point of contact for all Good... [Full Details] |
| Salary: Negotiable (20000 - 35000 £) |
| Regulatory And Drug Safety | Regulatory Affairs | Any Location (United Kingdom) | Details |
| Quality Assurance QA Associate Laboratory GLP - Contract Research Organisation – LONDON - £35,000 + Benefits
SUMMARY
This exciting new position is for an experienced Quality Assurance QA Associate who is looking for a challenging role within a growing organisation with involvement across the QA department and continual career progression. They offer an innovative product and are going... [Full Details] |
| Salary: Negotiable (30000 - 40000 £) |
| Regulatory And Drug Safety | Regulatory Affairs | West Sussex (United Kingdom) | Details |
| My client is one of the world's leading pharmaceutical companies. We are currently working with them in recruiting an Associate Director within their Health Economics and Outcomes Research group.
Job Description
- Execute HE&OR strategies that demonstrate overall product value (clinical and economic).
- Develop and integrate parameters necessary to demonstrate clinical, economic, and... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Regulatory Affairs | Any Location (United Kingdom) | Details |
| Quality Assurance QA Associate Laboratory GLP - Contract Research Organisation – LONDON - £35,000 + Benefits
SUMMARY
This exciting new position is for an experienced Quality Assurance QA Associate who is looking for a challenging role within a growing organisation with involvement across the QA department and continual career progression. They offer an innovative product and are going... [Full Details] |
| Salary: Negotiable (30000 - 40000 £) |
| Regulatory And Drug Safety | Regulatory Affairs | Manchester (United Kingdom) | Details |
| Clinical Quality Assurance (GCP) Auditor – International Clinical Research Organisation - £30,000+ and Excellent benefits - Northwest
SUMMARY
There is now the opportunity for an experienced Quality Auditor to join this hugely successful organisation in a senior role within their UK operation. It is a strategically hands-on opportunity in their Quality assurance function and team and being... [Full Details] |
| Salary: Negotiable (20000 - 30000 £) |
| Regulatory And Drug Safety | Regulatory Affairs | Any Location (Germany) | Details |
| SENIOR Clinical Quality Assurance (GCP) Auditor – International Clinical Research Organisation - >€90,000 + and Excellent benefits – GERMANY/SWITZERLAND
SUMMARY
There is now the opportunity for an experienced Quality Auditor to join this hugely successful organisation in a senior role within their European operation. It is a strategically hands-on opportunity in their Quality assurance... [Full Details] |
| Salary: Negotiable (60000 - 90000 £) |
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