Parexel, a leading global Clinical Research Organization (CRO), is dedicated to improving the world’s health through innovation in clinical trials, regulatory affairs, and medical writing. The company partners with biopharmaceutical organizations to bring new therapies to patients faster and more efficiently.
If you have strong proofreading skills, attention to detail, and experience in clinical documentation, this role offers an exciting opportunity to grow your career with a global leader.
🔍 Role Overview: Document Quality Reviewer II
As a Document Quality Reviewer (DQR) II at Parexel, you’ll ensure that clinical documents are error-free, scientifically accurate, and compliant with global regulatory standards. You will perform detailed reviews for grammar, format, and content integrity across diverse clinical deliverables.
📋 Key Responsibilities
- Conduct quality control (QC) of medical writing deliverables, ensuring accuracy and compliance with ICH-GCP and client guidelines.
- Edit and proofread clinical documents for grammar, consistency, and scientific accuracy.
- Perform formatting and style checks according to standard templates.
- Review documents such as protocols, clinical study reports (CSR), informed consent forms, and investigator brochures.
- Identify root causes of recurring document errors and suggest process improvements.
- Participate in training, mentoring, and knowledge-sharing sessions.
- Maintain compliance with corporate training, procedures, and workload trackers.
🎓 Required Qualifications
- Bachelor’s degree in Life Sciences, Health Sciences, or related field.
- Minimum 4 years of experience in medical writing, proofreading, or clinical documentation within CRO or pharma.
- Strong command of English grammar and technical writing.
- Familiarity with regulatory requirements, ICH-GCP guidelines, and the drug development process.
- Proficiency in MS Office, document management systems, and collaborative authoring tools.
💼 Preferred Skills
- Excellent attention to detail and language editing skills.
- Ability to manage multiple projects under tight deadlines.
- Strong interpersonal and communication skills.
- Understanding of clinical research, data accuracy, and scientific integrity.
🌐 Why Join Parexel?
- Work remotely from anywhere in India.
- Collaborate with global teams on cutting-edge clinical research projects.
- Opportunity for career advancement and professional certifications.
- Inclusive and values-driven company culture.
- Exposure to regulatory documentation for global submissions.
📝 How to Apply
