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Regulatory affairs officers new december 24 Jobs in Belfast

Last updated: 6 hours ago
  • Promoted
Regulatory Affairs Specialist

Regulatory Affairs Specialist

ARC Regulatory LtdBelfast, GB
Full-time
ARC's purpose is to expedite access to precision medicine clinical trials for patients globally.We fulfil our purpose through our dedicated team of experts with unparalleled domain knowledge, and t...Show moreLast updated: 10 days ago
Regulatory Reporting Operations Analyst

Regulatory Reporting Operations Analyst

G MASSBelfast, Northern Ireland, GB
£28,000.00–£30,000.00 yearly
Quick Apply
We are currently seeking operations professionals to join an financial services client of ours, based in Belfast.This role will be on a contract basis which will have an initial period of 6-months,...Show moreLast updated: 4 days ago
  • Promoted
Core Compliance Associate - 9 Month FTC

Core Compliance Associate - 9 Month FTC

TP ICAP GroupBelfast, Northern Ireland, United Kingdom
The TP ICAP Group is a world leading provider of market infrastructure.Our purpose is to provide clients with access to global financial and commodities markets, improving price discovery, liquidit...Show moreLast updated: 6 days ago
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Executive Director - Regulatory Risk

Executive Director - Regulatory Risk

Information Commissioner's OfficeBelfast, Northern Ireland, United Kingdom
Executive Director - Regulatory Risk.Apply locations : Wilmslow, Cheshire; Edinburgh; London; Belfast; Cardiff.Time left to apply : End Date : February 23, 2025 (22 days left to apply).Executive Direc...Show moreLast updated: 9 days ago
Locum GP

Locum GP

Mylocum GroupBelfast, GB
£45.00 hourly
Permanent
QUALIFICATIONS & JOB REQUIREMENTS : .Healthcare experience as aLocum GP .References covering the last 3 years of clinical employment. Significant experience as a qualified GP.Key skills : Compassion, T...Show moreLast updated: 30+ days ago
Public Affairs & Policy Manager

Public Affairs & Policy Manager

HappyJobsNIBelfast, United Kingdom
£40,000.00–£45,000.00 yearly
Full-time
Our client is Northern Ireland's leading homeless charity, dedicated to creating a society where everyone has a place to call home. Established over 50 years ago, they are renowned for their commitm...Show moreLast updated: 30+ days ago
Markets Controls Risk Analyst £600 / day 1 Year+ Contract BELFAST

Markets Controls Risk Analyst £600 / day 1 Year+ Contract BELFAST

AdeccoBelfast, Antrim
Full-time
Markets 1LOD Control Testing Business Risk Analyst.AVP / VP | Banking | £-£ / day Inside IR35 | BELFAST | HYBRID 3 days in the office per week | Initial Contract until December | Markets Control Testin...Show moreLast updated: 30+ days ago
Corporate Affairs and Engagement Director

Corporate Affairs and Engagement Director

Clarendon ExecutiveBelfast
£14.00–£18.00 hourly
Full-time
Corporate Affairs and Engagement Director – Belfast Harbour.Belfast Harbour, the city’s port authority, is a vital economic hub, handling a significant portion of Ireland’s maritime trade.Spanning ...Show moreLast updated: 30+ days ago
Policy and External Affairs Officer (NI)

Policy and External Affairs Officer (NI)

Ellwood AtfieldBelfast
£29,580.00–£31,817.00 yearly
Full-time
Ellwood Atfield has partnered with a leading UK health organisation who are looking to appoint a Policy and External Affairs Officer to join their Northern Ireland Office.The organisation works to ...Show moreLast updated: 30+ days ago
  • Promoted
Director, Regulatory Operations

Director, Regulatory Operations

PharmiwebBelfast, GB
Full-time
Director, Regulatory Operations.ICON plc is a world-leading healthcare intelligence and clinical research organization.We’re proud to foster an inclusive environment driving innovation and excellen...Show moreLast updated: 9 days ago
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  • New!
Senior Manager RAQA - Medical Devices

Senior Manager RAQA - Medical Devices

StrykerBelfast, Northern Ireland, United Kingdom
Full-time
Work Flexibility : Hybrid or Onsite.Are you ready to lead a dynamic team of regulatory and quality professionals towards excellence in ensuring market access, product quality, and compliance for lif...Show moreLast updated: 6 hours ago
FinOps Specialist (24 month FTC)

FinOps Specialist (24 month FTC)

Allen & OveryUnited Kingdom - Belfast
£70,000.00 yearly
Full-time
A&O Shearman is a new global industry-leading law firm, with nearly 50 offices in 29 countries worldwide.Our fluency in English law, US law, and the laws of the world’s most dynamic markets, enable...Show moreLast updated: 30+ days ago
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Band 3 Business Services Support Officers

Band 3 Business Services Support Officers

Brook StreetBelfast, Northern Ireland, United Kingdom
£11.67 hourly
Full-time
Do you have excellent IT skills and seeking a new role in Belfast City Centre?.Brook Street (UK) Ltd is currently seeking dedicated individual Band 3 System Support Officers on behalf of our esteem...Show moreLast updated: 7 days ago
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  • New!
Project Manager - Financial Markets Regulatory Transformation - VP

Project Manager - Financial Markets Regulatory Transformation - VP

Citigroup Inc.Belfast, Northern Ireland, United Kingdom
Full-time
Regulatory Project / Program Manager.Seeking a seasoned professional with a proven track record of Program / Portfolio Management within the Securities Markets and Banking (SMB) Technology, Banking or ...Show moreLast updated: 6 hours ago
Policy and External Affairs Officer

Policy and External Affairs Officer

hays-gcj-v4-pd-onlineBelfast
£30,698.00 yearly
Permanent
Hays are working with a public sector organisation to recruit for a Policy and External Affairs Officer on a Permanent basis. In this role you will support and promote thepany’s political, policy an...Show moreLast updated: 30+ days ago
  • Promoted
Regulatory Affairs Specialist

Regulatory Affairs Specialist

ARC RegulatoryBelfast, Northern Ireland, United Kingdom
Full-time
ARC's purpose is to expedite access to precision medicine clinical trials for patients globally.We fulfil our purpose through our dedicated team of experts with unparalleled domain knowledge, and t...Show moreLast updated: 6 days ago
HR Support Officers - Belfast

HR Support Officers - Belfast

Riada ResourcingBelfast
£11.39 hourly
Temporary
Northern Ireland Housing Executive - HR Support Officers - Belfast .Do you have HR experience and want to work in the Public Sector? Apply online or call Mairead on 028 2563 1555 to find out more.E...Show moreLast updated: 30+ days ago
Financial Accountant - 24 Months

Financial Accountant - 24 Months

VanrathBelfast
£43,000.00–£50,000.00 yearly
Temporary
Are you interested in working for a leading Public Sector employer for a period of 18 - 24 months? This is an excellent opportunity to join a stable team environment, with the opportunity to secure...Show moreLast updated: 30+ days ago
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Regulatory Affairs Specialist

Regulatory Affairs Specialist

ARC Regulatory LtdBelfast, GB
10 days ago
Job type
  • Full-time
Job description

ARC's purpose is to expedite access to precision medicine clinical trials for patients globally. We fulfil our purpose through our dedicated team of experts with unparalleled domain knowledge, and the important relationships we have developed with our global clients. We are a Belfast-based Clinical Research Organisation that specialises in delivering compliance excellence for companies in the precision medicine sector. We support many of the world's leading pharmaceutical R&D companies in implementing unapproved diagnostics in their clinical development programmes for patient selection or stratification, working as a strategic and integrated expert partner, taking full sponsor ownership of the IVD study being conducted in parallel with our clients' IND / IMP trial. ARC's team of experts cover IVD regulatory compliance, study design and approvals, quality assurance including vendor due diligence and management along with a team of clinical research experts who manage the IVD study, ensuring it is conducted in compliance with local and global GCP, and that the biomarker data is robust and reliable. To further support our growing client base and to expedite patient access to life-saving experimental medicines, ARC has developed and launched our SaaS platform, ARC360. ARC360 is transforming how organisations access regulatory intelligence and tailor study-specific information for using in vitro diagnostics to select and manage patients in IND trials. Powered by cutting-edge technologies and supported by a team of regulatory, quality, and clinical operations experts, ARC360 is designed to accelerate the initiation of complex clinical trials. Job Description To be an integral member and significant contributor to project team(s) in the development and delivery of global compliance solutions to client companies, ensuring that client objectives are met and exceeded at all times. This will require the utilisation of a platinum standard approach to regulatory research, internal and external stakeholder satisfaction as well as an innate work ethic and attention to detail that is aligned with the companys core values. Support the work of the company and project teams in the provision of specialised regulatory and quality assurance expertise to client companies, ensuring client expectations and interests are met. Research and prepare elements of regulatory submission documents on behalf of client companies, including but not limited to study risk determination requests, IDE submissions, 510(k), PMA, CE Technical Files and Design Dossiers, PMDA Briefing Documents and Submissions etc. Assist wider team in understanding the regulatory requirements for an investigational device in the set-up, management & conduct of IVD performance studies worldwide. Manage and keep up to date information relating to regulatory requirements for IVD performance studies and maintain the companys web-based clinical trial planning tool. Conduct gap analyses on behalf of client companies and prepare associated reports Contribute to the preparation of global guidance documents and white papers. Contribute to the preparation of other regulatory documents on behalf of client companies (e.g., Performance Evaluation Plans / Reports, Investigator Brochures, etc). As required, take advantage of professional networking opportunities to promote the company and its services to appropriate parties. Undertake continuing professional development activity to ensure awareness of current quality and regulatory standards. Contribute to ARC company culture initiatives to maintain a positive and engaging workforce. Any other duties, within reason and capability, as determined by company management. Essential Criteria Engineering or Scientific honours degree or equivalent (10+ years) relevant industry experience 5+ years experience of working in a medical device / IVD manufacturing or regulatory environment Experience with IVD / CDx design and development, from feasibility to approval Knowledge of regulations in key global markets as they pertain to IVD and / or CDx devices (e.g. EU / US) Experience of leading global regulatory submissions (e.g. EU / FDA) Experience developing and maintaining technical documentation (IVDD / IVDR) or design history file documentation (FDA) Experience developing global regulatory strategies for IVD devices Skills : Regulatory Affairs IVDR CDx