Remote Medical Writer Job at Parexel | Work From Home Opportunity | Apply Now!

Parexel is a leading global Contract Research Organisation (CRO) dedicated to accelerating the development of innovative therapies. Professionals collaborate with pharmaceutical, biotechnology, and healthcare companies worldwide to deliver clinical research, regulatory consulting, and medical writing solutions. Known for scientific excellence, quality, and innovation, Parexel provides employees with opportunities to work on impactful projects that improve patient outcomes worldwide.

About the role

This Remote Medical Writer position offers an excellent opportunity for professionals passionate about scientific communication and clinical research. As a Medical Writer I, you will prepare, review, and deliver clinical and regulatory documents while working remotely from India. This role combines scientific expertise, regulatory knowledge, and collaboration with cross-functional global teams.

Responsibilities

• Author, edit, and review clinical and regulatory documents, including Clinical Study Reports (CSRs), Interim Study Reports, Informed Consent Forms (ICFs), Safety Update Reports, and Patient Narratives.
• Conduct literature searches and scientific reviews to support document development.
• Analyze and interpret clinical study data to prepare high-quality scientific content.
• Ensure compliance with ICH-GCP guidelines, SOPs, templates, and regulatory requirements.
• Perform quality checks to ensure data accuracy, consistency, and document integrity.
• Collaborate with cross-functional teams including Clinical Operations, Biostatistics, Data Management, Regulatory Affairs, and Medical Affairs.
• Support document review cycles, manage timelines, and address stakeholder feedback.

Requirements

• Bachelor’s or Master’s degree in Medicine, or a related healthcare discipline.
• Experience within a CRO, pharmaceutical, biotechnology, healthcare, or medical communications organisation is preferred.

Skills

• Strong clinical and scientific writing skills.
• Good understanding of clinical research, drug development, and regulatory guidelines.
• Experience with medical writing, clinical documentation, or medical communications.
• Excellent written and verbal communication skills.
• Strong attention to detail and organisational skills.
• Proficiency in Microsoft Word, Excel, SharePoint, and document management systems.
• Ability to manage multiple projects and work effectively in a collaborative environment.

Location: Remote (India) | Department: Medical Writing | Job Type: Full-Time | Job ID: R0000044155