Average salary: £137,094 /yearly
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£47k - £63k per annumEstimated
We’re currently recruiting for a Regulatory Clinical Trial Strategy & Submissions Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory Affairs team on an initial 12 Month basis to be based at their office in Maidenhead/hybrid....
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£39k - £53k per annumEstimated
...Role: Regulatory Affairs Associate Location: Maidenhead / M4 corridor.
Salary: Very competitive salary on offer
Planet Pharma are... ...with 6-24 months regulatory experience!
Role summary:
Manage the operational and technical aspects of regulatory affairs for...
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£38k - £51k per annumEstimated
Role: Regulatory Affairs Associate Location: Salary: Very competitive salary on offer
Planet Pharma are supporting a leading large global... ...regulatory professional with 6-24 months regulatory experience!
Manage the operational and technical aspects of regulatory affairs...
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For contractors
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£42k - £53k per annumEstimated
...healthier lives and we are proud to be a Great Place to Work .
Job Description
We are now recruiting a Senior Regulatory Affairs Manager supporting Europe and reporting to the Regulatory Affairs Director, Europe for Oncology.
By integrating AbbVie you...
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Full time
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Local area
£49k - £63k per annumEstimated
...of registration strategy to ensure the regulatory approval of commercially successful pharma... ...product maintenance and lifecycle management, in line with legal/regulatory requirements... ...Pharmaceutical industry experience in Regulatory Affairs or R&D
European regulatory experience...
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Full time
£47k - £63k per annumEstimated
...at . Follow @abbvie on Twitter , Facebook , Instagram , YouTube and LinkedIn .
Job Description
Senior Government Affairs Manager
Based in the offices in Maidenhead with flexible working (3/2 model)
Reporting to the Head of Government Affairs.
Highly...
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Flexible hours
Allergan
Maidenhead, Berkshire
4 days ago
£25k - £33k per annumEstimated
...SRG are currently looking for a Regulatory Administrator for a Global Pharmaceutical Company who have opened a new vacancy within their... ...tasks with a keen eye for detail.
Key Responsibilities:
Managing the diary of the Regulatory Director and assisting with other...
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Flexible hours
...patients across the globe. We are looking for a Study Start-Up Project Manager to be 100% home based anywhere in the UK . This role would suit... ...and organizational skills Skilled knowledge of local regulatory environment and submission and approval processes, and understanding...
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£34k - £46k per annumEstimated
...and Contractor Members. They help maintain the ISO9001 Quality Management System, Avetta’s SSIP Membership and ISO17020 UKAS Accreditation... ...:
Ability to interpret and make decisions based on regulatory industry best practices (HSE Legislation), and/or Operator requirements...
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£97k - £131k per annumEstimated
...Collaboration Tools and Lead of the Centre Of Excellence:
Manage the lifecycle of DevOps solutions
escalations and facilitate... ...including non-employees) are trained and complying with the appropriate regulatory guidelines (e.g. cGMP), global I&T procedures, I&T standards, I&...
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£44k - £59k per annumEstimated
...world´s leading pharma companies, you will be one of the primary Regulatory Medical Writers , project leading the Development Cycle for... ...coordinate functional leads and reviewers from the Biostatistics, Data Management, Programming, Clinical Leadership and Project Physician teams....
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£80 - £100 per hour
...contractor.
Your new role
You will be joining a team of 4 as a Regulatory Labelling Lead consultant to create and implement strategies... ...level.
You will be responsible for leading the creation and management of documents throughout the product lifecycle, including the...
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£44k - £57k per annumEstimated
...world´s leading pharma companies, you will be one of the primary Regulatory Medical Writers , project leading the Development Cycle for... ...Skeleton Report.
~ Facilitate Comment resolution meetings, to manage conflicting comments early and ensuring smooth protocol...
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£45k - £62k per annumEstimated
...Description
The Health Technology Assessment (HTA) Manager reports into the HTA Lead and will be based in our... ...and other Market Access colleagues, Medical Affairs, Government Affairs, Patient Relations, Regulatory Affairs and Commercial Leads.
Accountable for the...
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Flexible hours
£47k - £63k per annumEstimated
...more than 20 therapeutic areas. We are looking for a full time QA Manager to join our Quality Assurance EMEA team.
Ensure the... ...improvement initiatives to drive efficiencies and effectiveness of Regulatory Compliance & Quality Assurance (RC&QA) processes
Lead and effectively...
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Full time
Contract work
£35k - £47k per annumEstimated
...accountants in Maidenhead who are looking to add a Personal Tax Assistant Manager to their team.
Working within the private client tax team,... ...(Accounts, Business Management & payroll) to ensure client affairs are co-ordinated and delivered on time
CTA Part or Fully...
£36k - £48k per annumEstimated
...accountants in Maidenhead who are looking to add a Personal Tax Assistant Manager to their team.
Working within the private client tax team,... ...(Accounts, Business Management & payroll) to ensure client affairs are co-ordinated and delivered on time
CTA Part or Fully...
...Description
About This Role
The Senior Medical Liaison Manager will be field/customer-facing (50%). You will be the medical and... ....
In additional you will have project/office-based medical affairs (50%) responsibility where you will proactively contribute, enrich...
Part time
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Local area
£49k - £66k per annumEstimated
...patients across the globe.
We are looking for a full time QA Manager to join our Quality Assurance EMEA team.
Essential Job Duties... ...improvement initiatives to drive efficiencies and effectiveness of Regulatory Compliance & Quality Assurance (RC&QA) processes
Lead and...
Full time
Contract work
£52k - £70k per annumEstimated
...solutions across more than 20 therapeutic areas. Senior Clinical Data Manager (oncology trials) - FSP - fully home-based anywhere in EMEA... ...operations.
Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological...
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