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Act as a lead writer across multiple projects, overseeing timelines, quality, and team resourcing. Coach and mentor junior writers, contributing to team knowledge sharing and best practice. Proven experience as lead writer across at least 3 document types (e.

This role offers the opportunity to work in a high-impact environment with a global client base, excellent support systems, and the ability to work remotely or flexibly.

We’re looking for a highly experienced and detail-oriented Senior Payroll Officer to manage and execute payroll operations within the fast-paced utilities and construction sectors. With a strong understanding of TUPE legislation and complex payroll system implementations, you’ll play a critical r...

Employment Solicitor - Remote | Flexible Hours Location: Fully Remote | Flexible Hours Salary: £40-70,000 Experience: NQ+ Full-time | Part-time This is a rare opportunity offering excellent work-life balance, with flexible working days and hours tailored to your lifestyle. ABOUT T...

We are recruiting on behalf of a well-established and highly respected firm, known for delivering exceptional conveyancing services with a strong reputation for quality and client care. Key Responsibilities: - Manage property transactions from instruction through to completion, ensuring a smo...

Registered Manager Homecare Bury, Greater Manchester £38,000 - £40,000 per annum Full-time, permanent position TRC is working with a great, private business, one of the leading providers of home care in the North of England and has been for the last 20 years. We are working hand in hand to...

We are really proud to say that in 2024, Outcomes First Group were officially certified as a ‘Great Place to Work’ for the fifth year running. *You’ll work 80% of your contractual hours for 100% of your pay, giving you more time to do the things that make you happy. 4DWW is subject to success...

Proven experience as a lead author on multiple regulatory documents, including at least 3 of the following: protocols, clinical study reports, clinical summaries, clinical overviews, investigator brochures, narratives, briefing documents, or regulatory response documents. Advise clients and colle...

Your new role /n /nJoining a team that operates nationally, this regulatory/health and safety solicitor role will see you handle a range of contentious and non-contentious regulatory matters for clients across a number of sectors. You will be involved in corporate manslaughter cases and will deal...

Excellent opportunity for a lawyer with experience in regulatory, environmental and/or health and safety to join a FTSE 100 business based in the West Midlands. You will have a high profile role within an established and experienced team advising on a variety of regulatory, civil and criminal inv...

As a Senior Regulatory Medical Writer, you will independently lead the development of a wide range of core regulatory documents across various therapeutic areas. Independently produce a range of high-quality regulatory documents (e. Minimum of 5 years' regulatory writing experience in a medical c...

Senior Compliance Consultant – Financial Crime & Regulatory Compliance (Payment Services & E-Money). Audits (financial crime, regulatory, safeguarding). AML, sanctions, fraud & regulatory compliance.

As a Senior Regulatory Medical Writer, you will independently lead the development of a wide range of core regulatory documents across various therapeutic areas. Independently produce a range of high-quality regulatory documents (e. Minimum of 5 years' regulatory writing experience in a medical c...

As a Senior Regulatory Medical Writer, you will independently lead the development of a wide range of core regulatory documents across various therapeutic areas. Senior Regulatory Medical Writer. This is a unique opportunity to join a high-performing regulatory writing team, with exposure to inte...

Strong understanding of regulatory writing standards and processes (e. This is a fantastic opportunity to contribute to meaningful regulatory submissions across a variety of therapeutic areas, working with a highly collaborative and well-established team. This position involves the development of...

To support in this development we are seeking a satellite regulatory and licencing manager, who will focus on the management and meeting of our regulatory compliance obligations across the EU. Lead on the regulatory and licencing strategy for Europe, including ensuring that licences are applied f...

You will work closely with internal teams and external clients to ensure that deliverables meet both scientific and regulatory standards. Write and edit a variety of regulatory documents (e. Ensure all documents are clear, accurate, and aligned with relevant regulatory guidelines and client expec...

Act as a subject matter expert on global regulatory requirements, including for ATMPs, ensuring company-wide compliance and integrating relevant regulatory intelligence. Lead regulatory interactions with authorities such as the FDA, EMA, and national agencies, while overseeing the preparation and...

As a Senior Regulatory Medical Writer, you will independently lead the development of a wide range of core regulatory documents across various therapeutic areas. This is a unique opportunity to join a high-performing regulatory writing team, with exposure to international projects, complex docume...

Reporting to the Regulatory Affairs Manager, you will play a key role in supporting global regulatory submissions, maintaining compliance documentation, and ensuring adherence to regulatory standards for medical devices in the EU, US, and other markets. Regulatory Affairs role within the medical ...

The ideal candidate will be an experienced Regulatory Solicitor with a background in handling insurance-related claims and a proven track record in regulatory law. The firm is well known for delivering high-quality legal services to both individuals and businesses, with a strong reputation for ou...

Provide critical support in developing global regulatory strategy, planning and execution of global investigational submissions and manages lifecycle regulatory activities in alignment with the Global Regulatory Lead (GRL). Research and apply regulatory intelligence and knowledge of strategic opt...

About the Role: As a Senior Regulatory Medical Writer, you will independently lead the development of a wide range of core regulatory documents across various therapeutic areas. Senior Regulatory Medical Writer. This is a unique opportunity to join a high-performing regulatory writing team, with ...

As a Senior Regulatory Medical Writer, you will independently lead the development of a wide range of core regulatory documents across various therapeutic areas. Independently produce a range of high-quality regulatory documents (e. Minimum of 5 years' regulatory writing experience in a medical c...

Due to the development and expansion of the firm, they are now seeking to appoint an experienced Health & Safety Regulatory Solicitor to support the Partner, dealing with regulatory cases and inquest work. The firm is recognised for its outstanding client care and high-quality Crime and Regulator...

You will work closely with internal teams and external clients to ensure that deliverables meet both scientific and regulatory standards. Write and edit a variety of regulatory documents (e. Ensure all documents are clear, accurate, and aligned with relevant regulatory guidelines and client expec...

The Regulatory Labelling Lead role is part of a project with a leading biopharmaceutical company focused on developing innovative treatments for rare and ultra-rare genetic diseases. Guiding the labeling team to develop and maintain Core Date sheets, USPI, SmPC and associated Patient Labeling doc...

To provide high-quality, concise, and accurate regulatory documentation that meets the expectations of both clients and regulatory authorities. Author regulatory documents across various therapeutic areas, ensuring outputs are clear, factual, scientifically accurate, and free from over-interpreta...

About the Role: As a Senior Regulatory Medical Writer, you will independently lead the development of a wide range of core regulatory documents across various therapeutic areas. This is a unique opportunity to join a high-performing regulatory writing team, with exposure to international projects...

Senior Regulatory Affairs Associate – Class III Devices | PMA Submissions | Remote + Monthly Onsite in Oxford | Equity + £100M Backed Start-up. Senior Regulatory Affairs Associate. Regulatory team and help take a breakthrough neuromodulation device through PMA submission and into the market.

The Regulatory Labelling and Artwork Specialist role is part of a project with a leading biopharmaceutical company focused on developing innovative treatments for rare and ultra-rare genetic diseases.

As a Senior Regulatory Medical Writer, you will independently lead the development of a wide range of core regulatory documents across various therapeutic areas. Senior Regulatory Medical Writer. This is a unique opportunity to join a high-performing regulatory writing team, with exposure to inte...

Advise on regulatory aspects of payment services for both bank and non-bank PSPs and e-money issuers. Minimum of 5 years PQE within a Financial Regulatory team, with strong knowledge of payment services and experience working with e-money businesses. Ability to draft regulatory provisions related...

Write and edit a variety of regulatory documents (e. Ensure all documents are clear, accurate, and aligned with relevant regulatory guidelines and client expectations. Conduct background research to confirm references and stay aligned with current regulatory requirements.

Write and edit a variety of regulatory documents (e. Ensure all documents are clear, accurate, and aligned with relevant regulatory guidelines and client expectations. Conduct background research to confirm references and stay aligned with current regulatory requirements.

Act as a reviewer and signatory during review of labeling ensuring that content complies with regulatory requirements. Facilitate cross-functional and team awareness and understanding of regulatory issues as appropriate. Significant hands-on registration experience associated with development, ma...

CTD clinical summaries, investigator brochures) across multiple therapeutic areas Ensure all documents are clear, accurate, and aligned with relevant regulatory guidelines and client expectations Review and quality-check clinical documentation, data outputs, and other supporting materials Liaise ...

Professional growth and development: You’ll have the opportunity to work on a diverse range of projects, from writing and editing regulatory documents to providing oversight for outsourced deliverables to our clients. Our services include device development and CE/UKCA marking certification, glob...

As a Senior Regulatory Medical Writer, you will independently lead the development of a wide range of core regulatory documents across various therapeutic areas. Strong understanding of ICH and regulatory authority requirements. Senior Regulatory Medical Writer.

This well-known biotech is looking for an experienced Regulatory Affairs Manager to join their established EU Regulatory Affairs team. As EU Senior Regulatory Affairs Manager, you will support the creation of strategy and execution plans and manage regulatory submissions (e. As EU Senior Regulato...

About the Role: As a Senior Regulatory Medical Writer, you will independently lead the development of a wide range of core regulatory documents across various therapeutic areas. BSc or PhD in life sciences (PhD preferred) Strong understanding of ICH and regulatory authority requirements Experienc...

We are looking to recruit Senior Regulatory Writers with at least 3 years' experience as a regulatory writer within the pharmaceutical industry and/or a medical writing agency. Complete Regulatory is part of IPG Health Medical Communications, who is home to the world’s most celebrated and awarded...

Healthcare Regulatory Partner | Manchester | up to £165k + Bonus + Excellent Benefits. A Tier 1 Legal 500 firm with a stellar reputation in healthcare law is looking to appoint a senior hire—Legal Director or Partner level—into its expanding Healthcare Regulatory team in Manchester. This is a r

Proven experience as a lead author on multiple regulatory documents, including at least 3 of the following: protocols, clinical study reports, clinical summaries, clinical overviews, investigator brochures, narratives, briefing documents, or regulatory response documents. Senior Regulatory Writer...

Over years 5 years working on a range of Regulatory documents.

The ideal candidate will be an experienced Regulatory Solicitor with a background in handling insurance-related claims and a proven track record in regulatory law. This is an exciting opportunity to handle a broad range of regulatory matters on behalf of insurers representing large charities, pub...

Ensure all documents are clear, accurate, and aligned with relevant regulatory guidelines and client expectations. Conduct background research to confirm references and stay aligned with current regulatory requirements. Previous experience producing regulatory documentation within a medical commu...

Significant hands-on registration experience associated with development, maintenance, and commercialization activities within Regulatory affairs. Understand regulatory implications of product strategy with regards to the product label & assessment. Ability to interpret and apply global and local...