Find Senior clinical data Jobs in Dublin, D

Senior Clinical Editor
IQVIA —Dublin, County Dublin
- Doctoral degree
- English
- Research
Clinical Data Management Lead, home-based
IQVIA —Dublin, County Dublin
- Remote
- Customer service
- Project management
- Bachelor's degree
Global Scientific Lead - Clinical Outcome Assessment (COA) Strategy Consulting - Multiple locations - Hybrid/Home-based
IQVIA —Dublin, County Dublin
- Doctoral degree
- English
- Research
Principal Consultant - Regulatory Affairs
NNIT A/S —Dublin, County Dublin
- Spanish
- Sales
- English
Senior Statistical Programmer
IQVIA —Dublin, County Dublin
- Remote
- Computer Science
- Bachelor's degree
- Quality control
Sr/Principal Statistician (Sponsor-dedicated) Many possible locations (EMEA) - R Shiny experience
サイネオス・ヘルス —Dublin, County Dublin
- Doctoral degree
Group Head of Talent Acquisition
Bon Secours Health System Ireland —Dublin, County Dublin
- Full-time
- Social media management
- Microsoft Office
- Analysis skills
13d
Sr Director, Real-World Data Sales
IQVIA —Dublin, County Dublin
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Research Support Coordinator
Irish Cancer Society —DUBLIN 4, County Dublin
- €37,000 a year
- Full-time
- Hybrid work
- Microsoft Word
- Word processing
- Research
- Annual leave
- Employee assistance program
Quick apply
9d
Senior Sonographer – Obstetric Ultrasound Development Role
Medica —Dublin, County Dublin
- Full-time
- Mentoring
- Communication skills
- Teaching
Quick apply
12d
Senior Manager, Core Labelling Strategy
Viatris —Northern Cross, County Dublin
- Full-time
- Research
- Analysis skills
- Bachelor's degree
Senior Director, Planning and Resource Management
ICON Plc —Dublin, County Dublin
- Full-time
- Bachelor's degree
- Leadership
- Communication skills
5d
Senior Manager, Commercial Strategy, Industry Relations
Optum —Dublin, County Dublin
- Full-time
- Management
- Bachelor's degree
- Communication skills
5d
Senior Medical Scientist / Senior Biomedical Scientist Histology
Eurofins Ireland Clinical Diagnostics —DUBLIN 18, County Dublin
- Full-time
- Master's degree
- Bachelor's degree
- Communication skills
- Employee assistance program
- Sick pay
Quick apply
Senior Radiation Therapist
Blackrock Health Hermitage Clinic —Lucan, County Dublin
- Full-time
- Research
- Clinic
- Bachelor's degree
Quick apply
Health & Social Care Transformation Senior Consultant, Hybrid
Deloitte —Dublin, County Dublin
- €55,000 a year
- Full-time
- Hybrid work
Technical Product Manager
Optum —Dublin, County Dublin
- Full-time
- Computer Science
- Bachelor's degree
- Agile
Senior Software Development Engineer
Solventum —Dublin, County Dublin
- Full-time
- Hybrid work
- DevOps
- SQL
- AWS
- Relocation assistance
Senior Site Reliability Engineer - Ireland
Heidi —Dublin, County Dublin
- Full-time
- Hybrid work
- DevOps
- AWS
- Mentoring
- Work from home
Discharge Coordinator
Blackrock Health Blackrock Clinic —Dublin, County Dublin
- Full-time
- Clinic
- Communication skills
- Annual leave
- Employee assistance program
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

senior clinical data jobs in dublin, d

Senior Clinical Editor

Clinical Data Management Lead, home-based

Global Scientific Lead - Clinical Outcome Assessment (COA) Strategy Consulting - Multiple locations - Hybrid/Home-based

Principal Consultant - Regulatory Affairs

Senior Statistical Programmer

Sr/Principal Statistician (Sponsor-dedicated) Many possible locations (EMEA) - R Shiny experience

Group Head of Talent Acquisition

Sr Director, Real-World Data Sales

Research Support Coordinator

Senior Sonographer – Obstetric Ultrasound Development Role

Senior Manager, Core Labelling Strategy

Senior Director, Planning and Resource Management

Senior Manager, Commercial Strategy, Industry Relations

Senior Medical Scientist / Senior Biomedical Scientist Histology

Senior Radiation Therapist

Health & Social Care Transformation Senior Consultant, Hybrid

Technical Product Manager

Senior Software Development Engineer

Senior Site Reliability Engineer - Ireland

Discharge Coordinator

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