Senior Medical Writer

Responsibilities

• Lead preparation, review and editing of clinical study protocols, CSRs, investigator brochures and regulatory submissions

• Collaborate with clinical research, biostatistics, regulatory affairs and medical affairs teams

• Contribute to publication plans, abstracts, posters and manuscripts

• Mentor and coach junior medical writers

Requirements

• Bachelor's degree in a relevant scientific or healthcare field

• Strong interpretation and summarization of clinical trial data and statistical analyses

• Understanding of ICH-GCP, FDA and EMA regulatory requirements

• Ability to manage multiple projects in a deadline-driven environment

• Excellent interpersonal and communication skills

Benefits

• Competitive base salary and performance incentives

• Medical, dental and vision coverage where applicable

• Retirement and pension plans

• Life assurance and disability coverage

• Learning and development opportunities

About the Company

• ICON is a clinical research organisation and the world's largest FSP organisation, with over 90 sponsor partnerships.