Find clinical trial manager Jobs in dublin, d

Senior Clinical Editor
IQVIA —Dublin, County Dublin
- Full-time
- Doctoral degree
- English
- Research
Clinical Analyst
Teckro Limited —Dublin, County Dublin
- Full-time
- Hybrid work
- Microsoft Excel
- Data analysis skills
- Master's degree
- Gym membership
- Life insurance
Quick apply
CNM 1 Endocrine Research
Beaumont Hospital —Dublin, County Dublin
- Full-time
- Research
- Clinic
- No degree
9d
Senior Clinical Engagement Project Manager
Teckro Limited —Dublin, County Dublin
- Full-time
- Hybrid work
- Project management
- Presentation skills
- Bachelor's degree
- Gym membership
- Life insurance
Quick apply
Senior Clinical Data Analyst
Teckro Limited —Dublin, County Dublin
- Full-time
- Hybrid work
- Microsoft Excel
- Data analysis skills
- Master's degree
- Gym membership
- Life insurance
Quick apply
Senior Clinical Data Scientist
Novartis —Dublin, County Dublin
- Full-time
- Master's degree
- Organisational skills
Principal Clinical Data Scientist
Novartis —Dublin, County Dublin
- Full-time
- Master's degree
- Organisational skills
- Agile
GMDP Quality Assurance Manager
WEP Clinical —Dublin, County Dublin
- Full-time
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
Clinical Development Director - Renal
Novartis —Dublin, County Dublin
- Full-time
- Doctoral degree
- Writing skills
- No degree
12d
Senior Principal Clinical Data Scientist
Novartis —Dublin, County Dublin
- Full-time
- Master's degree
- Mentoring
- Organisational skills
Neurovascular Research Fellow
National Institute for Bioprocessing Research and Training (NIBRT) —Dublin, County Dublin
- Doctoral degree
- Data analysis skills
- Research
- Annual leave
Clinical Trials Nurse
Beacon Hospital —Dublin, County Dublin
- Full-time
- Nursing
- Research
- Patient care
Quick apply
Programme Lead
Teckro Limited —Dublin, County Dublin
- Full-time
- Hybrid work
- Hotel
- Project management
- No degree
- Gym membership
- Life insurance
Quick apply
13d
Neurovascular Postdoctoral Researcher
National Institute for Bioprocessing Research and Training (NIBRT) —Dublin, County Dublin
- Remote
- Doctoral degree
- Research
- Analysis skills
- Annual leave
HR Administrator
Uniphar Wholesale Limited —DUBLIN 24, County Dublin
- Full-time
- Continuous improvement
- Human resources
- Organisational skills
Quick apply
1d
Director and Head of EMEA Emerging Biopharma Sales, IQVIA Central Laboratories
IQVIA —Dublin, County Dublin
- Full-time
- Analysis skills
- Communication skills
- Negotiation
Business Support Specialist 12 month Fixed Term Contract
AllPhar Services Limited —DUBLIN 24, County Dublin
- Full-time
- Microsoft Powerpoint
- Microsoft Excel
- Analysis skills
Quick apply
Mid-Level Backend Software Engineer
Teckro Limited —Dublin, County Dublin
- Full-time
- Hybrid work
- Computer Science
- System design
- Hotel
- Gym membership
- Life insurance
Quick apply

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Senior Clinical Editor

IQVIA -
Dublin, County Dublin

Apply Now

Job details

Full-time

Qualifications

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

Full job description

Dublin, Ireland | Full time | Home-based | R1543145

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

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clinical trial manager jobs in dublin, d

Senior Clinical Editor

Clinical Analyst

CNM 1 Endocrine Research

Senior Clinical Engagement Project Manager

Senior Clinical Data Analyst

Senior Clinical Data Scientist

Principal Clinical Data Scientist

GMDP Quality Assurance Manager

Clinical Development Director - Renal

Senior Principal Clinical Data Scientist

Neurovascular Research Fellow

Clinical Trials Nurse

Programme Lead

Neurovascular Postdoctoral Researcher

HR Administrator

Director and Head of EMEA Emerging Biopharma Sales, IQVIA Central Laboratories

Business Support Specialist 12 month Fixed Term Contract

Mid-Level Backend Software Engineer

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