Lead the development and execution of medical writing strategies for clinical research projects, contributing to the advancement of innovative treatments and therapies
Job Summary
Lead the development and execution of medical writing strategies for clinical research projects, contributing to the advancement of innovative treatments and therapies.
Collaborate closely with cross-functional teams to interpret and analyze clinical trial data, summarize scientific findings, and participate in the planning and execution of clinical development programs.
ICON offers a range of additional benefits focused on well-being and work-life balance, including various annual leave entitlements, health insurance, and retirement planning.
Matching Summary
Lead the development and execution of medical writing strategies for clinical research projects, contributing to the advancement of innovative treatments and therapies.
Skills & Requirements
Must-have
medical writing strategies
clinical study documents
interpreting clinical trial data
regulatory requirements
ICH-GCP, FDA, EMA
Nice-to-have
fostering a culture of excellence
collaboration and continuous learning
influencing decision-making processes
work life balance opportunities
Key Requirements
Bachelor's degree in scientific discipline
Proficiency in writing, editing, proofreading
Experience interacting with regulatory agencies
Ability to manage multiple projects simultaneously