Medical Writer Jobs in Brillex Clinical Research Pvt Ltd - Ahmedabad, Gujarat

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Medical Writer Jobs in Brillex Clinical Research Pvt Ltd - Ahmedabad, Gujarat

work outline icon2 - 3 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Brillex Clinical Research Pvt Ltd

time outline iconAhmedabad, Gujarat, India

Posted on 28-01-2026

1 Vacancy

Description

  1. Job Title: Medical Writer
  2. Qualification: BPharm/MPharm
  3. Location: Brillex Clinical Research Pvt Ltd - Ahmedabad, Gujarat
  4. Work Experience: 2 to 3 Years

Job Description

  1. Prepare and review medical and scientific documents.
  2. Write clinical study reports, protocols, investigator brochures.
  3. Develop regulatory documents and submissions.
  4. Create manuscripts, abstracts, and presentations.
  5. Summarize clinical and scientific data accurately.
  6. Ensure compliance with regulatory and ethical guidelines.
  7. Perform literature reviews and data analysis.
  8. Edit and proofread documents for accuracy and clarity.
  9. Coordinate with clinical, regulatory, and research teams.
  10. Maintain document version control and timelines.

Take this opportunity to join Brillex Clinical Research Pvt Ltd - Ahmedabad, Gujarat as a Medical Writer in Ahmedabad, Gujarat and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.

Category

Others

Preferred Education

MPharm (Master Of Pharmacy)BPharm (Bachelor Of Pharmacy)

Key Skills

DocumentationCoordination SkillsGood Communication SkillsTeamwork

About Organization

Brillex Clinical Research Pvt Ltd, Ahmedabad, Gujarat, is a growing clinical research organization focused on quality, compliance, and ethical research practices. The company is expanding its documentation and research support team and inviting applications for this role. The responsibilities include preparing and reviewing clinical documents, protocols, study reports, and regulatory submissions, ensuring accuracy and compliance with ICH-GCP and regulatory guidelines, coordinating with clinical and regulatory teams, and maintaining proper documentation standards. This opportunity offers strong exposure to clinical research documentation, professional skill development, and long-term career growth in a structured and supportive research environment.

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