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 strategic and scientific input to clinical development programs

• Develop publication plans, abstracts, posters and manuscripts for journals and conferences

• Mentor and coach junior medical writers

Requirements

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

• Experience interpreting and summarizing complex clinical trial data and statistics

• Strong understanding of ICH-GCP, FDA and EMA regulatory requirements

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

• Excellent interpersonal and communication skills

Benefits

• Competitive base salary and performance related incentives

• Medical, dental and vision coverage where applicable

• Retirement and pension plans

• Life assurance and disability coverage

• Employee assistance programmes and learning opportunities

About the Company

ICON is a global healthcare intelligence and clinical research organisation focused on bringing new medicines and treatments to patients faster.