Find Master/project manager Jobs in Dublin, D

Senior Clinical Editor
IQVIA —Dublin, County Dublin
- Doctoral degree
- English
- Research
Project Manager
Cushman & Wakefield —Dublin, County Dublin
- Full-time
- Engineering
- Supervising experience
- Project management
1d
Project Director - Rail
Amey Ltd —DUBLIN 1, County Dublin
- Master's degree
- Project management
- Bachelor's degree
- Annual leave
- Gym membership
Quick apply
Sr. Software Engineering Manager – Infrastructure and Security
Intel —Leixlip, County Kildare
- €130,100–€203,200 a year
- Full-time
- Doctoral degree
- Computer Science
- Engineering
Sr. Technical Project Manager
iCims —DUBLIN 2, County Dublin
- Azure
- Master's degree
- AWS
- Annual leave
- Life insurance
Account Manager, LCS (French, English)
Google —Dublin, County Dublin
- €76,000–€78,000 a year
- Full-time
- Sales
- English
- Master's degree
Product Deployment Engineer Manager, gTech
Google —Dublin, County Dublin
- €182,000–€197,000 a year
- Full-time
- Java
- Master's degree
- SQL
8d
HR Lead
Dovida Ireland —Dublin, County Dublin
- Full-time
- Master's degree
- Bachelor's degree
- Human resources
Senior Manager Logistics Process Integration
Bristol-Myers Squibb —Dublin, County Dublin
- Full-time
- Microsoft Excel
- Master's degree
- Analysis skills
- Annual leave
- Work from home
Financial Planning Manager
Elwood Roberts —Dublin, County Dublin
- €80,000–€90,000 a month
- Full-time
- Microsoft Office
- Finance
- Master's degree
Quick apply
Quality Engineer (NPI)
West Pharmaceutical Services —Dublin, County Dublin
- €51,000–€59,000 a year
- Engineering
- Manufacturing
- Communication skills
Senior Business Analyst
TestReach —Dublin, County Dublin
- Computer Science
- Master's degree
- Bachelor's degree
12d
Scrum Master
Glanbia Foods —DUBLIN 24, County Dublin
- Hybrid work
- Master's degree
- Bachelor's degree
- No degree
Clinical Tutor – Histopathology
RCPI —DUBLIN 2, County Dublin
- €500 a day
- Doctoral degree
- Microsoft Office
- Master's degree
Quick apply
Trial Master File Oversight Manager
Novartis —Dublin, County Dublin
- €55,370–€102,830 a year
- Full-time
- Bachelor's degree
- Conflict management
- Negotiation
Director - Consulting, Government & Public Sector (G&PS) - Advisory
PwC —Dublin, County Dublin
- Full-time
- Master's degree
- Business development
- Bachelor's degree
Clinical Document Management Learning Manager
Novartis —Dublin, County Dublin
- €55,370–€102,830 a year
- Full-time
- Hybrid work
- Research
- Bachelor's degree
- No degree
9d
Supply Chain Planner/ BA
Fonua Ltd —DUBLIN 18, County Dublin
- Microsoft Excel
- Engineering
- ERP systems
- Free parking
Quick apply
Regional Business Manager
Allianz —Blackrock, County Dublin
- Full-time
- Management
- Sales
- Master's degree
Director of Project Management
IPS-Integrated Project Services —DUBLIN 12, County Dublin
- Full-time
- Engineering
- Project management
- Bachelor's degree
9d

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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

master/project manager jobs in dublin, d

Senior Clinical Editor

Project Manager

Project Director - Rail

Sr. Software Engineering Manager – Infrastructure and Security

Sr. Technical Project Manager

Account Manager, LCS (French, English)

Product Deployment Engineer Manager, gTech

HR Lead

Senior Manager Logistics Process Integration

Financial Planning Manager

Quality Engineer (NPI)

Senior Business Analyst

Scrum Master

Clinical Tutor – Histopathology

Trial Master File Oversight Manager

Director - Consulting, Government & Public Sector (G&PS) - Advisory

Clinical Document Management Learning Manager

Supply Chain Planner/ BA

Regional Business Manager

Director of Project Management

I want to receive the latest job alerts for master/project manager in dublin, d

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