Sr Medical Writer

Sr. Medical Writer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. As a Senior Medical Writer at ICON, you will lead the development and execution of medical writing strategies for clinical research projects, contributing to the advancement of innovative treatments and therapies. What You Will Do: You will take ownership of medical writing deliverables, applying your expertise to complex challenges. Key responsibilities include: Leading the preparation, review, and editing of clinical study documents, including clinical study protocols, clinical study reports (CSRs), investigator brochures (IBs), and regulatory submissions, ensuring accuracy, clarity Collaborating closely with cross-functional teams, including clinical research, biostatistics, regulatory affairs, and medical affairs, to interpret and analyze clinical trial data, summarize scientific findings Participating in the planning and execution of clinical development programs, providing strategic input and scientific expertise to support the design, conduct, and interpretation of clinical studies and research initiatives. Contributing to the development of publication plans, abstracts, posters, and manuscripts for submission to peer-reviewed journals and presentation at scientific conferences Mentoring and coaching junior medical writers, providing guidance on best practices, writing techniques, and scientific principles, and fostering a culture of excellence, collaboration, and continuous learning within the medical writing team. Your Profile: You will have a strong foundation in medical writing, with the experience to work independently and guide others. Required qualifications and experience: Bachelor's degree in a relevant scientific discipline or healthcare-related field Proficiency in interpreting and summarizing complex clinical trial data, scientific research findings, and statistical analyses, with excellent writing, editing, and proofreading skills Strong understanding of regulatory requirements (e.g., ICH-GCP, FDA, EMA) governing the preparation and submission of clinical documents and publications, and experience in interacting with regulatory agencies during the review and approval process. Demonstrated ability to work effectively in a fast-paced, deadline-driven environment, managing multiple projects simultaneously and prioritizing tasks based on project timelines and deliverables. Excellent interpersonal and communication skills, with the ability to collaborate effectively with cross-functional teams, build relationships with key stakeholders, and influence decision-making processes. Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here. Are you a current ICON Employee? Please click here to apply

The Senior Medical Writer will lead the development and execution of medical writing strategies for clinical research projects, including the preparation of protocols, CSRs, and regulatory submissions. They will also collaborate with cross-functional teams to interpret clinical data and mentor junior staff to foster a culture of excellence.

Candidates must hold a bachelor's degree in a scientific or healthcare-related field and possess strong experience in interpreting complex clinical trial data. Proficiency in regulatory requirements such as ICH-GCP, FDA, and EMA is essential, along with excellent communication and project management skills.

• Competitive base salary • Performance related incentives • Medical coverage • Dental coverage • Vision coverage • Retirement plans • Pension plans • Life assurance • Disability coverage • Employee assistance programmes • Wellbeing resources • Learning and development opportunities

• Gestion de projetSouhaitée

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• Medical writing
• Clinical study protocols
• Clinical study reports
• Investigator brochures
• Regulatory submissions
• Clinical trial data interpretation
• Scientific writing
• Editing
• Proofreading
• ICH-GCP
• FDA regulations
• EMA regulations
• Project management
• Cross-functional collaboration
• Mentoring
• Strategic planning
• Regulatory Affairs
• Influencing Skills
• Continuous Development
• Medical Affairs
• Influencing Without Authority
• Ability To Meet Deadlines
• Planning
• Research
• Biostatistics
• Decision Making
• Pre-Clinical Development
• Clinical Research
• Clinical Trials
• Clinical Study Reports
• Communication
• Good Clinical Practices (GCP)
• Innovation
• Medical Writing
• Mentorship
• Regulatory Requirements
• Coaching
• Scientific Studies
• Timelines
• Writing
• Collaboration

• Healthcare
• Science & Research
• Management & Leadership
• Medical Writer
• Authors and Related Writers
• Technical Writers

Formation minimale

Baccalauréat

Expérience minimale

5+ ans

Langue de l’offre

anglais

Heures de travail

40 heures par semaine