Medical & Regulatory Writer | Clinical Research | Scientific Content Writer| Biotechnology

I am a Biotechnology postgraduate with 2+ years of experience in Clinical Research and a strong interest in Medical Writing, Regulatory Writing, and Pharmacovigilance. My experience has helped me develop a solid understanding of clinical trial documentation, study coordination, GCP principles, data quality, and regulatory processes.

To strengthen my transition into medical writing, I have completed specialized training in Medical Writing and Regulatory Writing, where I gained knowledge of clinical and regulatory documents, including Clinical Study Reports (CSR), Protocols, Investigator's Brochures (IB), Common Technical Document (CTD), PBRER, DSUR, Risk Management Plans (RMP), literature review, and scientific writing.

I enjoy transforming complex scientific and medical information into clear, accurate, and reader-friendly content while maintaining scientific integrity and regulatory compliance.

Work Terms

Communication: Prompt and professional communication throughout the project.
Available for discussions via Guru messages and scheduled online meetings when required.
Regular progress updates for long-term assignments.

Project Delivery: Committed to delivering quality work within agreed timelines.
Revisions included based on the original project scope.
All work is thoroughly reviewed before submission for accuracy and clarity.

Confidentiality: Client information and project materials will be treated as confidential.
Willing to sign a Non-Disclosure Agreement (NDA) if required.

Availability: Available for both short-term projects.
Flexible working hours to accommodate different time zones.

Payment: Open to fixed-price and hourly projects.
Milestone-based payments are preferred for larger assignments.