Informed Consent Writer

🔥 0 minutes ago

🔔 Pennsylvania – Remote

🔔 Pennsylvania – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

✏️ Content Writer

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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ICON plc

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1990

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

📋 Description

• Prepare, write, and edit clinical study reports (CSRs), clinical protocols, investigator brochures (IBs), and patient narratives • Conduct literature reviews, data analysis, and interpretation of clinical trial results • Support the development of scientific manuscripts, abstracts, and posters • Assist in reviewing and validating clinical data for accuracy, completeness, and consistency with study protocols, SOPs, and regulatory requirements • Participate in project meetings, teleconferences, and client interactions • Discuss project objectives, timelines, and deliverables • Provide input and feedback on document content, format, and presentation • Keep abreast of emerging trends, scientific developments, and regulatory updates in relevant therapeutic areas • Deliver medical writing work to a high standard while working closely with the team and stakeholders

🎯 Requirements

• Bachelor's degree in Life Sciences, Pharmacy, Medicine, or related field • Keen interest in medical writing, clinical research, and drug development processes • Excellent written and verbal communication skills • 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 • 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) • Familiarity with document management systems, reference management software, and statistical analysis tools preferred • Ability to work collaboratively as part of a multidisciplinary team • Ability to communicate effectively across different functional areas • Ability to 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 • Legal right to work in the country where the role is based

🏖️ 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