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Job Title: EU Regulatory Affairs Manager Department: Regulatory Affairs Location: Uxbridge, UK or Dublin, Ireland – 3x a week in the office Job Type: 12 Month Contract /FTC Remuneration: Up to £85,000/€90,000 This is a 12-month contract role, and you MUST be able to start this role within 4 weeks. An exciting opportunity to work for a global leading and prestigious Biotechnology company that is at the heart of science. They have a new opportunity and growing need for EU-specific expertise on the development programs, as well as to keep the company compliant on emerging EU legislation and processes, which has led to the need to create a new position based in our Dublin or London office. The role is positioned at the Manager/Senior Manager level to enable advanced regulatory input to interactions with EU Regulatory agencies and with our business partners. This role will be focussed on supporting development activities in the area of respiratory and inflammation. JOB RESPONSIBILITIES: • Assist Development teams and Regulatory management in developing strategies that are EU-appropriate and take advantage of EU regulatory systems and processes., • Provide leadership on both late and early-stage clinical development related process and strategy to ensure timely study conduct end to end., • Assist clinical teams in study start up and maintenance activities by leading all associated regulatory activities, including but not limited to submissions, addressing agency queries, managing compliance issues., • Take ownership of EU CTR applications, Study Start up and PIPS., • Provide leadership on MAA related process and strategy to ensure timely product approvals with competitively differentiated labelling., • Monitor emerging legislation and guidance in the EU and contribute to ensuring company-level awareness and compliance (where appropriate)., • Build the representation of EU regulatory function to EMA and EU National Agencies, as, • well as Alliance partners as required. JOB REQUIREMENTS: Education • Advanced degree in a scientific discipline master’s degree or Ph.D. Experience • Minimum of 5 years in Regulatory Affairs ideally in drug development., • Prior CTA submission experience., • Prior Cell Therapy experience is preferred., • Confident in leading EU strategy development., • Strong knowledge of the clinical research process and regulations/guidelines, • Strong organizational, interpersonal and communication skills, • Ability to manage multiple projects. For more information, please reach out to You MUST be UK/IRELAND based and hold the Full Right to Work

The role is positioned at the Manager/Senior Manager level to enable advanced regulatory input to interactions with EU Regulatory agencies and with our business partners. Job Title: EU Regulatory Affairs Manager. Assist Development teams and Regulatory management in developing strategies that are EU

Job Title: Senior Medical Writer, Clinical and Regulatory.Job Type: Initial 9 Month Contract /FTC.This is a 9 month contract role, and you MUST be able to start this role within 4 weeks.The Senior Medical Writer (SMW) works with team members and independently to write the content of clinical documen

Remote position based in England.Due to the rapid growth and expansion of business activities across multiple markets,.Arabic Financial Translator (English ↔ Arabic).My client operates as a global financial services organisation supporting experienced traders across a wide range of international m

Job Title: EU Regulatory Affairs Manager.Department: Regulatory Affairs.Location: Uxbridge, UK or Dublin, Ireland – 3x a week in the office.Job Type: 12 Month Contract /FTC.Remuneration: Up to £85,000/€90,000.This is a 12-month contract role, and you MUST be able to start this role within 4 wee

Children’s Home — Registered Manager (South region).Relocation support available for those willing to relocate.We are seeking an enthusiastic and determined Registered Manager to lead a residential children’s home.The successful candidate will head up a team, ensuring that children receive out

Job Title: Regulatory Affairs Training Manager – Regulatory Information Management (RIM).Description: 18-month Contract, Inside IR35.Location: Remote, 1x a month travel to West London.Rate: £430/day via umbrella engagement only.The RA Training Manager - RIM will have a key role in the success of

Why work with Cpl UK Healthcare?. Cpl UK Healthcare are a market-leader in recruiting AHP’s across the UK.

Senior Manager, Regulatory Labelling.Competitive Salary + Excellent Benefits.As a Senior Manager, Regulatory Labelling,.This includes inputting from a regulatory labelling perspective on developing and established drug programs and being accountable for driving global labelling strategies.This is a

Children’s Home — Registered Manager (South region).Relocation support available for those willing to relocate.We are seeking an enthusiastic and determined Registered Manager to lead a residential children’s home.The successful candidate will head up a team, ensuring that children

Technical Sales Manager – Imaging & Detector Systems - £70,000 + 20% bonus.A growing specialist imaging and detector systems company is seeking a.This role is ideal for someone with strong technical understanding (imaging, detectors, physics, engineering) and the commercial ambition to progress i

Why work with Cpl UK Healthcare?. Cpl UK Healthcare are a market-leader in recruiting AHP’s across the UK.

Our Client is hiring an experienced Packaging Engineering Project Manager to join their world-class manufacturing site in Cramlington, Northumberland.In this pivotal role, you will lead the delivery of advanced packaging solutions—driving and leading the design, installation, and commissioning of

Deputy Medical Director – Surgical Services (South Coast Region).An experienced medical leader to join the senior management team of a leading independent healthcare provider, overseeing surgical services across two high-performing South Coast sites.Part-Time (4–5 days per week) and flexible to

Job Title: EU Regulatory Affairs Manager.Department: Regulatory Affairs.Location: Uxbridge, UK or Dublin, Ireland – 3x a week in the office.Job Type: 12 Month Contract /FTC.Remuneration: Up to £85,000/€90,000.This is a 12-month contract role, and you MUST be able to start this role withi

CPL Executive Search has been retained as the exclusive search and selection (recruitment) company to look for a strong and passionate results orientated leader, with good strategic vision to lead the global activities for our Client’s Natural Food Ingredients business unit. Please note that CPL E

UK Commercial Excellence Manager – Global Pharmaceutical Company.Slough (3 days per week on-site).A global pharmaceutical company is seeking a Commercial Excellence Manager to lead its Business Excellence function and drive commercial performance across the organisation.Lead Business Excellence ac

Remote position based in England.Due to the rapid growth and expansion of business activities across multiple markets, my client is seeking an experienced, motivated, and technology-oriented individual for a full-time position as an Arabic Financial Translator (English Arabic).My client operates

Regulatory Affairs Manager/Snr Manager - UK Market.Hertfordshire, UK – Hybrid, 3x a week on site.This is an excellent opportunity to join a leading pharmaceutical business.In this position, you will be responsible for all aspects of the UK product portfolio for developing drugs and established pro

Sales Territory Business Manager.Location: Southwest England & Wales.The Immunology Territory Business Manager (TBM) will be responsible for managing the business for biologic in key accounts within their territory.TBMs will lead on local account planning across priority hospital accounts and the ov

Technical Sales Manager – Imaging & Detector Systems - £70,000 + 20% bonus.A growing specialist imaging and detector systems company is seeking a.This role is ideal for someone with strong technical understanding (imaging, detectors, physics, engineering) and the commercial ambition to progress i