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Are you passionate about scientific writing and clinical research? Parexel, a global leader in clinical development solutions, is hiring Medical Writer I/II professionals for its teams in Hyderabad and Bengaluru (with remote opportunities).
This role offers an excellent opportunity to contribute to the development of therapies that improve patients’ lives while building a rewarding career in medical writing.
Key Responsibilities
As a Medical Writer at Parexel, you will:
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- Author clinical documents including study reports, informed consent forms, and safety updates.
- Perform literature searches, review statistical outputs, and ensure compliance with SOPs and regulatory guidelines.
- Ensure quality control by maintaining accuracy, data consistency, and adherence to global regulatory standards.
- Provide medical editing and content review for draft and final documents.
- Manage medical writing projects, serving as client contact, coordinating team reviews, and driving timelines.
- Participate in training and compliance initiatives, supporting process improvement and knowledge sharing.
Qualifications & Skills
- Education: Bachelor’s degree in Life Sciences/Health Sciences (or equivalent).
- Experience: Prior experience in medical writing, regulatory documentation, or clinical research preferred.
- Strong knowledge of ICH-GCP guidelines and the drug development process.
- Proficiency in MS Office, document management systems, and collaborative authoring tools.
- Excellent communication, project management, and organizational skills.
- Fluent in English (written and spoken) with strong attention to detail.
Benefits of Working with Parexel
- Work in a global, collaborative environment with diverse projects.
- Gain exposure to regulatory submissions and clinical development processes.
- Opportunities for career growth, mentorship, and training.
- Flexible remote and hybrid work options.
- Competitive salary and benefits package.
How to Apply
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