Informed Consent Writer
As a Medical Writer I at ICON, you will the development and preparation of clinical trial documents, regulatory submissions, and scientific publications, contributing to the advancement of innovative treatments and therapies.
What You Will Do:Your role will involve delivering medical writing work to a high standard, working closely with your team and stakeholders.
Key responsibilities include:
- Collaborating with cross-functional teams to prepare, write, and edit clinical study reports (CSRs), clinical protocols, investigator brochures (IBs), patient narratives
- Conducting literature reviews, data analysis, and interpretation of clinical trial results to support the development of scientific manuscripts, abstracts, posters
- Assisting in the review and validation of clinical data, ensuring accuracy, completeness, and consistency with study protocols, standard operating procedures (SOPs), and regulatory requirements.
- Participating in project meetings, teleconferences, and client interactions to discuss project objectives, timelines, and deliverables, while providing input and feedback on document content, format, and presentation.
- Keeping abreast of emerging trends, scientific developments, and regulatory updates in relevant therapeutic areas
Your Profile:You will bring relevant medical writing experience, along with the following qualifications and skills.
Required qualifications and experience:
- Bachelor's degree in Life Sciences, Pharmacy, Medicine, or related field, with a keen interest in medical writing, clinical research, and drug development processes.
- Excellent written and verbal communication skills, with the ability to translate complex medical and scientific information into clear, concise, and engaging content tailored to diverse audiences.
- Strong attention to detail and organizational skills, with the ability to manage multiple tasks simultaneously, prioritize workload effectively, and meet project deadlines in a fast-paced environment.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and familiarity with document management systems, reference management software, and statistical analysis tools preferred.
- Demonstrated ability to work collaboratively as part of a multidisciplinary team, communicate effectively across different functional areas, and adapt to changing project requirements and priorities.
- Motivated self-starter with a passion for learning and professional growth, committed to delivering high-quality work and contributing to the success of clinical research initiatives.
Rewards & BenefitsICON 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.
