Medical Writer

Senior Medical Writer

Experience:

Salary :

Preferred Notice Period

Opportunity Type:

Placement Type:

(*Note: This is a requirement for one of Uplers' Clients)

Must have skills required :

CRO, writing scientific/regulatory/ clinical documents, MS Office suite

Tatvacare (One of Uplers' Clients) is Looking for:

Role Overview Description

Position Summary

Key Responsibilities

• Prepare, review, and edit a variety of scientific and regulatory documents, including clinical study reports, protocols, investigator brochures, patient narratives, informed consent forms, manuscripts, abstracts, and posters.
• Ensure documents comply with ICH-GCP, regulatory guidelines, client specifications, and internal SOPs.
• Collaborate with cross-functional teams including clinical, regulatory, pharmacovigilance, and biostatistics to obtain necessary inputs for document preparation.
• Interpret clinical and scientific data accurately and present it in a clear, concise, and scientifically sound manner.
• Support regulatory submissions by authoring CTD modules and other submission-related documents.
• Conduct thorough literature reviews to support scientific writing and study-related documents.
• Assist in quality control and peer review of documents to ensure accuracy, consistency, and compliance.
• Manage timelines, prioritize tasks, and ensure timely delivery of high-quality documents.
• Participate in project meetings and provide updates on document progress and timelines.
• Contribute to the development and maintenance of templates, style guides, and SOPs for medical writing.

Desired Candidate Profile

• Minimum 3 years of hands-on experience as a medical writer in a CRO, pharmaceutical, or healthcare setting.
• Advanced degree in Life Sciences, Medicine, Pharmacy, or related discipline (PhD/MD/MBBS/MSc preferred).
• Proven track record of writing scientific, clinical, and regulatory documents.
• Excellent command over English language, with strong attention to detail, grammar, and scientific accuracy.
• Familiarity with ICH-GCP, regulatory requirements (FDA, EMA, DCGI), and submission processes.
• Proficiency in MS Office Suite and experience with reference management tools (e.g., EndNote, Mendeley).
• Strong analytical skills with the ability to interpret complex clinical and scientific data.
• Ability to manage multiple projects simultaneously and meet tight deadlines.
• Excellent communication and interpersonal skills to work effectively with cross-functional teams.
• Experience in mentoring or guiding junior medical writers will be an added advantage.

Career Growth

This position offers the opportunity to work on global projects across diverse therapeutic areas, gain exposure to regulatory submissions, and contribute to high-impact scientific publications. The Senior Medical Writer will also have the potential to progress into leadership roles such as Medical Writing Team Lead with responsibilities for mentoring, training, and strategic planning.

How to apply for this opportunity:

Easy 3-Step Process:

2. Upload updated Resume & Complete the Screening Form

About Uplers:

Our goal is to make hiring and getting hired reliable, simple, and fast. Our role will be to help all our talents find and apply for relevant product and engineering job opportunities and progress in their career.

(Note: There are many more opportunities apart from this on the portal.)

So, if you are ready for a new challenge, a great work environment, and an opportunity to take your career to the next level, don't hesitate to apply today. We are waiting for you!