7 May 2026

Senior Clinical Editor

IQVIA

Amsterdam

7 May 2026

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Senior Clinical Editor performs quality control review of Medical Writing deliverables, ensuring accuracy and compliance. Provides leadership and training to staff. Requires at least 8 years experience with clinical trial documentation.

RemoteFull-timeSeniorClinical Study ReportsClinical Trial Documentation

Senior Clinical Editor

Apply

RemoteFull-timeSeniorClinical Study Reports

Salary

Not specified

Work Location

Amsterdam, North Holland, Netherlands, NL

Work Model

Remote

Experience Required

8 years

Employment Type

Full-time

Experience Level

Typically at least 8 years experience

Core Qualifications

Technical (Must-have)

clinical study reportsclinical trial documentationdrug developmentquality controlregulatory knowledgeEnglish languageAdobe AcrobatprotocolsMedical WritingMicrosoft Office

Soft Skills

attention to detailorganizational skillstime managementcommunicationleadershipmentoringproblem solvingproactivityadaptabilityteamwork

Key Responsibilities

•Conduct quality control review of Medical Writing deliverables
•Document findings in accordance with procedures
•Liaise with document authors
•Develop quality tools such as checklists and guidelines
•Provide training and mentoring within QC group
•Manage resourcing of QC tasks
•Lead QC team meetings and share lessons learned
•Contribute to budget proposals for QC tasks
•Manage daily assignments and workload
•Keep abreast of current data and regulatory knowledge

Senior Clinical EditorMedical WritingQuality ControlClinical ResearchPharmaceuticalRemoteFull-timeNetherlandsLife Sciences

Core Qualifications

Technical (Must-have)

clinical study reportsclinical trial documentationdrug developmentquality controlregulatory knowledgeEnglish languageAdobe AcrobatprotocolsMedical WritingMicrosoft Office

Soft Skills

attention to detailorganizational skillstime managementcommunicationleadershipmentoringproblem solvingproactivityadaptabilityteamwork

Key Responsibilities

•Conduct quality control review of Medical Writing deliverables

•Document findings in accordance with procedures

•Liaise with document authors

•Develop quality tools such as checklists and guidelines

•Provide training and mentoring within QC group

•Manage resourcing of QC tasks

•Lead QC team meetings and share lessons learned

•Contribute to budget proposals for QC tasks

•Manage daily assignments and workload

•Keep abreast of current data and regulatory knowledge