Find Fraud manager Jobs in Ireland

Senior Clinical Editor
IQVIA —Dublin, County Dublin
- Doctoral degree
- English
- Research
Senior Manager, Supplier Compliance & Third Party Risk Management (TPRM) – Global Procurement
Bristol-Myers Squibb —Dublin, County Dublin
- Full-time
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- Master's degree
- Analysis skills
- Annual leave
Vendor Startup Manager IRT – Single Sponsor (home-based)
IQVIA —Dublin, County Dublin
- Remote
- Continuous improvement
- Budgeting
- Communication skills
Assoc Director, Quality Management - Client Dedicated Clinical Compliance Optimization Lead
IQVIA —Dublin, County Dublin
- English
- Microsoft Office
- Bachelor's degree
2d
Senior Manager CSCQ, Qualified Person
Bristol-Myers Squibb —Dublin, County Dublin
- Full-time
- Microsoft Excel
- Bachelor's degree
- In-person
- Annual leave
10d
Forensic Accounting Manager - Deals - Forensic Claims, Investigations and Audit
PwC —Dublin, County Dublin
- Full-time
- Data analysis skills
- Analysis skills
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Merchant Acquiring Pricing Manager (VP)
JPMorganChase —DUBLIN 2, County Dublin
- Full-time
- Microsoft Excel
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Senior Manager, Serialization Data Operations
Bristol-Myers Squibb —Dublin, County Dublin
- Full-time
- Microsoft Excel
- ERP systems
- Bachelor's degree
2d
Talent Acquisition Partner
Daon Inc —Dublin, County Dublin
- Hybrid work
- Recruiting
- Analytics
Quick apply
Clinical Research Associate - Ireland
IQVIA —Dublin, County Dublin
- Nursing
- English
- In-person
Senior Software Engineer - PathMakers (Patient Care Systems)
Medtronic —Galway, County Galway
- €65,600–€98,400 a year
- Full-time
- Azure
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On-Chain Risk Strategy Manager
Coins.ph —County Cavan
- Hybrid work
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Quick apply
Senior Solutions Consultant
Trulioo —Dublin, County Dublin
- Full-time
- Hybrid work
- English
- AI
- Communication skills
- Annual leave
Advertising Operations Manager
Koneo Mobile Inc. —Dublin, County Dublin
- Microsoft Excel
- English
- Analysis skills
Quick apply
Remote Sales Representative
Medtronic —Dublin, County Dublin
- €52,800–€79,200 a year
- Full-time
- Remote
- Sales
- Recruiting
- Negotiation
10d
Data Team Lead/Senior Data Team Lead
IQVIA —Dublin, County Dublin
- Analysis skills
- Bachelor's degree
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Senior French Speaking Customer Operations Agent
FNZ —Dublin, County Dublin
- Full-time
- Microsoft Excel
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- English
Transfer Agency – Registration Services, Associate 2
State Street —Kilkenny, County Kilkenny
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Microsoft Office
- Work from home
3d
Microbiology and Sterility Assurance Lead
Baxter —Dublin, County Dublin
- Management
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- Continuous improvement
- Annual leave
2d
A&H Travel Complex Adjuster
AIG Europe S.A. (Ireland branch) —DUBLIN 1, County Dublin
- Full-time
- Customer service
- Administrative experience
- Communication skills
Quick apply

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Senior Clinical Editor

IQVIA -
Dublin, County Dublin

Apply Now

Job details

Qualifications

Doctoral degree
English
Research
Microsoft Office
Master's degree
Bachelor's degree
Quality control
Adobe Acrobat
Time management

Full job description

Job Overview

Performs quality control review of Medical Writing deliverables from internal and external authors to ensure accuracy, consistency, and compliance with format and style requirements. Provides leadership, training, and guidance to staff, and assists in resource management.

Essential Functions

Is a subject matter expert within the group and a source of advice and information to IQVIA staff on quality control processes;
Conduct quality control (QC) review of a wide range of Medical Writing deliverables for both internal and external customers, including complex and substantial documents, with limited guidance and consistent high quality and efficiency;
Document findings clearly, in accordance with defined procedures and checklists;
Liaise promptly with document authors in case of questions or missing sources;
Provide service metrics and scores, as required;
Develop quality tools such as checklists, quality guidelines, standards and scoring methodology to meet project specific needs;
May have responsibility for resourcing of QC tasks within the team;
Take a leading role in providing training, guidance, and mentoring within the QC group;
May take a formal supervisory role in managing QC staff and/or contract resources;
Take a leading role in proposing, developing, evaluating, and implementing process changes and tools and monitoring their adoption and benefits;
Take a leading role in QC team meetings and ensuring that lessons learned are shared and consistent approaches are applied;
Contribute to budget proposals for QC tasks and maintain a clear understanding of the time and resources needed for tasks within remit;
May take a leadership role for a stand-alone QC project, lead the team, and be the primary contact with the customer;
May participate in project team meetings and liaise directly with the customer on QC issues, as appropriate and with senior support as needed;
Take responsibility for on-time delivery of QC review comments;
Manage daily assignments, planning and directing work, and take responsibility for managing workload for assigned projects and tasks, in collaboration with senior staff;
Keep abreast of current data, trends, medical writing (MW)/regulatory knowledge, developments and advances in area of drug development/MW.

Qualifications

Bachelor's Degree Life sciences related discipline or related field Req
Master's Degree Life sciences related discipline or related field Pref
Ph.D. Life sciences related discipline or related field Pref
Typically, at least 8 years experience working with clinical trial documentation in a research environment, including significant experience of performing quality control (QC) review of clinical trial-related documents, defining and refining processes, and training and developing others.

Experience

Requires in-depth understanding of the structure, format, and purpose of a wide range of MW deliverables and the importance of consistency, clarity, and accuracy versus sources. Req
Careful attention to detail, accuracy, and consistency;
Impeccable English language skills and ability to detect and correct grammatical, spelling, and language errors;
Ability to understand scientific/medical documents and identify deficiencies, errors and inconsistencies;
Familiarity with the structural and content requirements of clinical study reports, protocols, and similar documents;
Proactivity and advanced organizational and time management skills and ability to prioritize workload effectively with commitment to deadlines;
Ability to communicate clearly, concisely, and effectively in English, both in writing and verbally, and confidence in using a range of communication methods to achieve results;
Good understanding of clinical drug development and the functions, steps, and processes involved;
Advanced understanding of the nature and purpose of Medical Writing deliverables;
Ability to provide clear and effective guidance and training in the form of written instructions, presentations, and one-to-one discussion;
Ability to provide thorough, appropriate, and sensitive feedback to less experienced colleagues;
Confident use of Microsoft Office and Adobe Acrobat;
Ability to quickly establish and maintain effective working relationships with co-workers, managers, and customers at a range of seniority levels.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Apply Now

Refine Your Search

fraud manager jobs in ireland

Senior Clinical Editor

Senior Manager, Supplier Compliance & Third Party Risk Management (TPRM) – Global Procurement

Vendor Startup Manager IRT – Single Sponsor (home-based)

Assoc Director, Quality Management - Client Dedicated Clinical Compliance Optimization Lead

Senior Manager CSCQ, Qualified Person

Forensic Accounting Manager - Deals - Forensic Claims, Investigations and Audit

Merchant Acquiring Pricing Manager (VP)

Senior Manager, Serialization Data Operations

Talent Acquisition Partner

Clinical Research Associate - Ireland

Senior Software Engineer - PathMakers (Patient Care Systems)

On-Chain Risk Strategy Manager

Senior Solutions Consultant

Advertising Operations Manager

Remote Sales Representative

Data Team Lead/Senior Data Team Lead

Senior French Speaking Customer Operations Agent

Transfer Agency – Registration Services, Associate 2

Microbiology and Sterility Assurance Lead

A&H Travel Complex Adjuster

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