Note: The job is a remote job and is open to candidates in USA. ICON Strategic Solutions is a global healthcare intelligence and clinical research organization dedicated to accelerating the delivery of new medicines and treatments. The Informed Consent Writer will be responsible for developing and preparing clinical trial documents, regulatory submissions, and scientific publications, contributing to the advancement of innovative treatments and therapies.
Responsibilities
- 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
Skills
- 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
- Familiarity with document management systems, reference management software, and statistical analysis tools
Benefits
- 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
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