Technical Writer – Clinical Research & Scientific Documentation

Company Overview

Company overview not specified.

Job Summary

We are seeking a scientifically trained Technical Writer to support our dermatology clinic and research center's clinical research, scientific documentation, and innovation initiatives. The successful candidate will work closely with dermatologists, clinical researchers, formulation scientists, and external collaborators to prepare high-quality scientific and regulatory documentation.

Responsibilities

• Clinical Research Documentation

  • Draft and edit clinical study protocols, case report forms, informed consent documents, investigator brochures, and study reports.
  • Prepare documentation required for ethics committee and institutional review board submissions.
  • Maintain study master files and ensure documentation complies with applicable guidelines and standards.
  • Support clinical audit and inspection readiness activities.

• Scientific Documentation

  • Conduct comprehensive literature reviews and evidence syntheses.
  • Draft scientific abstracts, conference posters, oral presentations, and publication summaries.
  • Coordinate with investigators, statisticians, and collaborators during manuscript development and submission.

• Scientific Data Management

  • Review and interpret scientific literature and clinical data.
  • Develop evidence-based summaries for internal decision-making and research planning.
  • Ensure scientific accuracy and consistency across all research documents.

Qualifications

• Required

  • Master’s degree or higher in Pharmacy, Life Sciences, Biotechnology, Pharmaceutical Sciences, Biomedical Sciences, or related disciplines.
  • 2–5 years of experience in scientific, clinical, or medical writing.
  • Strong understanding of clinical research methodology and scientific publishing.
  • Excellent scientific writing and editing skills.
  • Experience conducting literature searches using scientific databases.

• Preferred

  • Experience in dermatology, cosmetic science, or pharmaceutical research.
  • Familiarity with Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, and publication standards.
  • Experience supporting patent-related scientific documentation.

Preferred Skills

• Knowledge of regulatory submission processes.
• Familiarity with electronic document management systems.
• Strong communication and collaboration skills.

Experience

• 2–5 years of relevant experience in scientific, clinical, or medical writing.

Environment

• The position is based in Chennai, India and is a full-time role within a clinical and research-oriented environment.

Salary

Salary information not specified.

Growth Opportunities

Growth opportunities within the company not specified.

Benefits

Benefits information not specified.