Medical Writer, Associate

🕒 Yesterday

🇮🇳 India – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🏥📝 Medical Writer

🚫👨‍🎓 No degree required

👻 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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Clario

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

Founded 1973

🏥 Healthcare

💼 Consulting

📦 Logistics

💰 Private Equity Round on 2019-10

Healthcare • Consulting • Logistics

Clario is a company specializing in accelerating clinical trials from initiation to implementation through advanced technologies and services. Since 2018, Clario has revolutionized endpoint analyses in clinical trials by integrating over 30 artificial intelligence-enabled solutions across more than 600 active trials, enhancing data quality and patient privacy while expediting data collection processes. Clario provides a comprehensive clinical trial management platform, offering solutions such as eCOA, cardiac safety, medical imaging, precision motion, and respiratory services in various therapeutic areas including oncology, cardiology, and neurology. Known for its global reach, Clario supports clinical trials in over 100 countries with a strong focus on decentralized and hybrid trial models. The company's commitment to patient safety and innovation is reflected in their over 26,000 trials and involvement in numerous new drug approvals.

📋 Description

• Support study startup activities by creating, organizing, and maintaining study-specific Medical Writing and Medical Communications documentation • Review study protocols and imaging requirements to ensure accurate interpretation of study procedures, schedules, and operational requirements • Create, update, and finalize study documentation, including Site Manuals, supporting forms, labels, and study-specific communication materials • Develop, review, and maintain compliance-related documentation, including Notes to File, protocol amendment impact assessments, corrections, and other quality records • Create and maintain source documentation and electronic clinical forms • Prepare meeting agendas, meeting minutes, and action item documentation • Attend internal and external meetings related to study startup documentation, compliance activities, and operational deliverables • Support maintenance and enhancement of Medical Communications resources, databases, web content, and document repositories • Assist with project closeout activities and archive study documentation according to company procedures and regulatory requirements • Support development, review, and maintenance of SOPs, Work Instructions, templates, and training materials • Assist with review and update of reader training materials, study training content, and educational resources • Maintain study tracking tools, document status reports, and Medical Writing databases • Provide guidance and support to project teams regarding document development processes, templates, and study documentation requirements • Contribute to continuous improvement initiatives focused on quality, compliance, efficiency, and operational excellence

🎯 Requirements

• Bachelor's degree in Life Sciences, Biological Sciences, Physical Sciences, Pharmacy, Healthcare, Clinical Research, or a related scientific discipline preferred • 1+ years of medical writing experience preferred; equivalent clinical research or scientific documentation experience will be considered • 2+ years of experience within pharmaceutical, biotechnology, clinical research, healthcare, medical imaging, or related industries preferred • Understanding of medical, clinical research, regulatory, or scientific writing principles • Knowledge of clinical trial terminology, medical imaging concepts, and clinical research processes preferred • Strong proficiency with Microsoft Office applications, including Word, Excel, PowerPoint, Outlook, and related productivity tools • Excellent written and verbal communication skills with the ability to communicate effectively in English • Strong attention to detail with exceptional proofreading, editing, and document quality review skills • Demonstrated ability to manage multiple projects, priorities, and deadlines simultaneously • Strong organizational, documentation, and time management skills • Ability to work independently while collaborating effectively within cross-functional and global teams • Adaptability and flexibility in managing changing priorities within a fast-paced environment • Professional, proactive, and customer-focused approach with a commitment to quality and continuous improvement

🏖️ Benefits

• Competitive pay and incentives • Provident fund • Medical insurance • Engaging employee programs and local events • Modern office spaces and remote work flexibility • Opportunities for professional growth and career development within a global organization