Medical Writer & Clinical Trials Assistant Jobs – Immediate Joiners

If you are looking to grow your career in medical writing or clinical research, this is a great opportunity to work with leading teams offering hands-on exposure to clinical documentation, regulatory writing, and clinical trial operations. These openings are ideal for candidates with 1+ year medical writing experience or 6–12 months experience in clinical research, and who are ready to join immediately.

The hiring organization is inviting qualified Life Science graduates to apply for the roles of Medical Writer and Clinical Trials Assistant (CTA) for Bengaluru and Hyderabad locations.

💼 1. Medical Writer – Hyderabad

Responsibilities

• Assist in drafting and formatting clinical and regulatory documents: Protocols, CSRs, IBs, ICFs.
• Support senior writers with literature reviews and scientific data summaries.
• Maintain accuracy, clarity, and compliance with ICH/GCP and writing guidelines.
• Update document templates, style guides, and reference libraries.
• Collaborate with clinical, regulatory, and data management teams.
• Participate in review meetings and support responses to internal/client feedback.
• Track document versions, timelines, and submission history.
• Prepare slide decks, abstracts, and scientific communication materials.
• Stay updated with therapeutic area knowledge and guidelines.

Qualifications

• Degree in Life Sciences, Pharmacy, Biotechnology, or related fields.
• 1+ year experience in Medical Writing.
• Good understanding of clinical research and regulatory documentation.
• Strong scientific writing and literature review skills.
• Excellent communication and time-management abilities.

💼 2. Clinical Trials Assistant (CTA) – Bengaluru

Responsibilities

• Perform day-to-day administrative and documentation activities for clinical trials.
• Maintain Trial Master File (TMF) accuracy and completeness.
• Prepare, handle, file, and archive clinical trial documents.
• Assist CRAs and RSU teams with clinical supplies tracking.
• Support CRF tracking, query management, and data flow activities.
• Act as the central communication point for clinical team interactions.
• Participate in study file reviews for compliance.
• May accompany CRAs on site visits after required training.

Qualifications

• Bachelor’s degree in Life Sciences/Pharmacy or equivalent.
• 6 months to 1 year of experience in clinical research or CTA role.
• Strong MS Office knowledge (Word, Excel, PowerPoint).
• Good English communication and organizational skills.
• Knowledge of GCP & ICH guidelines.

✨ Benefits

• Opportunity to work with experienced clinical and medical writing teams.
• Exposure to global regulatory documentation and TMF processes.
• Skill development in scientific writing, clinical trial coordination, and compliance.
• Supportive learning environment for career enhancement.

📩 How to Apply

Eligible candidates can send their updated resumes to:
👉 career@samahitha.com