IQVIA UK is seeking a Lead Medical Writer to manage advanced writing projects, including clinical study reports and protocols. The ideal candidate will have a strong background in life sciences, with a minimum of three years of relevant experience and expertise in medical writing, statistical analysis, and regulatory compliance
Job Summary
Acts as Lead Medical Writer on more advanced writing projects, preparing assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines.
Manages day-to-day workload, identifies project needs, tracks timelines, implements customer requests, and keeps manager/senior staff abreast of progress.
Keeps abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practice (GCP), along with developments and advances in drug development/medical and/or technical writing.
Matching Summary
Match Score: 85
IQVIA UK is seeking a Lead Medical Writer to manage advanced writing projects, including clinical study reports and protocols. The ideal candidate will have a strong background in life sciences, with a minimum of three years of relevant experience and expertise in medical writing, statistical analysis, and regulatory compliance.
Skills & Requirements
Must-have
Lead Medical Writer
complex clinical study reports
protocols
customer requirements
agreed timelines
Good Clinical Practice (GCP)
drug development knowledge
Nice-to-have
provide feedback to peers
deliver basic level training
guidance to more junior colleagues
propose revisions to SOPs
Key Requirements
Bachelor's Degree in life sciences
at least 3 years of prior relevant experience
Familiarity with clinical study reports, protocols
Ability to identify deficiencies, errors, and inconsistencies