Find Clinical data science Jobs in Dublin, D

Senior Clinical Editor
IQVIA —Dublin, County Dublin
- Doctoral degree
- English
- Research
Assoc Director, Quality Management - Client Dedicated Clinical Compliance Optimization Lead
IQVIA —Dublin, County Dublin
- English
- Microsoft Office
- Bachelor's degree
2d
Senior Real World Data Scientist
Alexion Pharmaceuticals,Inc. —Dublin, County Dublin
- Master's degree
- SQL
- EMR systems
Precision Medicine Director
Novartis —Dublin, County Dublin
- Full-time
- Hybrid work
- Research
- Leadership
- Annual leave
Director, Product Management - Clinical Content & Repository Services
Optum —Dublin, County Dublin
- Full-time
- Computer Science
- Master's degree
- AI
EHR Systems Analyst
UPMC —Dublin, County Dublin
- Clinic
- IT
- Annual leave
Director Global Costing Center of Excellence
Bristol-Myers Squibb —Dublin, County Dublin
- Full-time
- Microsoft Excel
- ERP systems
- Finance
2d
Principal Consultant - Regulatory Affairs
NNIT A/S —Dublin, County Dublin
- Spanish
- Sales
- English
Principal Biostatistician - Biomarker (EMEA Remote)
サイネオス・ヘルス —Dublin, County Dublin
- Doctoral degree
- Master's degree
- No degree
Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting
IQVIA —Dublin, County Dublin
- Doctoral degree
- Research
- Master's degree
Principal Statistical Programmer
IQVIA —Dublin, County Dublin
- Remote
- Computer Science
- Bachelor's degree
- Quality control
Evidence Generation Lead BBU& OBU
AstraZeneca —Dublin, County Dublin
- Doctoral degree
- Master's degree
- Leadership
6d
Global Labelling Manager, Content (Neuroscience)
Novartis —Dublin, County Dublin
- €55,370–€102,830 a year
- Full-time
- Hybrid work
- Communication skills
10d
Senior LIMS Consultant
NNIT A/S —Dublin, County Dublin
- Spanish
- English
- IT
Global Labelling Associate Director, Content (Established Products)
Novartis —Dublin, County Dublin
- €75,880–€140,920 a year
- Full-time
- Hybrid work
- Continuous improvement
12d
BDS Manufacturing Operations Lead
Alexion Pharmaceuticals,Inc. —Dublin, County Dublin
- Doctoral degree
- Engineering
- Master's degree
Principal Statistical Programmer - FSP (Permanent Homebased)
IQVIA —Dublin, County Dublin
- Computer Science
- Bachelor's degree
Director of Commercial Analytics & Insights
Optum —Dublin, County Dublin
- Full-time
- Azure
- Computer Science
- SQL
Manager Corporate Drug Regulatory Affairs (12 month agency contract)
Viatris —Northern Cross, County Dublin
- Full-time
- English
- Bachelor's degree
- Communication skills
Executive Director, Global Patient Safety Sciences Delivery
Regeneron —Dublin, County Dublin
- €172,500–€288,300 a year
- Doctoral degree
- Master's degree
- Business
- Annual leave

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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

clinical data science jobs in dublin, d

Senior Clinical Editor

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

Senior Real World Data Scientist

Precision Medicine Director

Director, Product Management - Clinical Content & Repository Services

EHR Systems Analyst

Director Global Costing Center of Excellence

Principal Consultant - Regulatory Affairs

Principal Biostatistician - Biomarker (EMEA Remote)

Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting

Principal Statistical Programmer

Evidence Generation Lead BBU& OBU

Global Labelling Manager, Content (Neuroscience)

Senior LIMS Consultant

Global Labelling Associate Director, Content (Established Products)

BDS Manufacturing Operations Lead

Principal Statistical Programmer - FSP (Permanent Homebased)

Director of Commercial Analytics & Insights

Manager Corporate Drug Regulatory Affairs (12 month agency contract)

Executive Director, Global Patient Safety Sciences Delivery

I want to receive the latest job alerts for clinical data science in dublin, d

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