Medical Writer

Why This Role Matters

Croissance Clinical Research operates in the Clinical Research Organization (CRO) sector, supporting pharmaceutical and healthcare companies in clinical trials and regulatory processes. Medical Writing plays a crucial role in ensuring accurate, compliant, and scientifically sound documentation for regulatory submissions, clinical studies, and research publications.
This position is ideal for professionals who have strong scientific writing skills and want to contribute directly to clinical research documentation, regulatory compliance, and scientific communication within the pharmaceutical and life sciences industry.

Job Description

Croissance Clinical Research is inviting applications for the position of Medical Writer in Hyderabad. The selected candidate will be responsible for preparing, reviewing, and managing scientific and regulatory documents in compliance with industry standards and regulatory guidelines.
The role requires strong writing capabilities, understanding of clinical research processes, and the ability to translate complex scientific data into clear, structured, and compliant documentation.

Key Features of the Role

• Opportunity to work in the Clinical Research (CRO) sector
• Exposure to clinical trial documentation and regulatory writing
• Competitive compensation package
• Professional growth in medical and scientific writing
• Collaborative work environment with clinical and regulatory teams

Responsibilities Required

• Preparing clinical study documents such as protocols, CSRs, IBs, and informed consent forms
• Drafting regulatory submission documents as per applicable guidelines
• Reviewing and editing scientific content for clarity, accuracy, and compliance
• Collaborating with clinical research, regulatory, and data management teams
• Ensuring documentation aligns with ICH-GCP and regulatory standards
• Managing document timelines and version control
• Conducting literature reviews and summarizing scientific findings
• Supporting publication writing and medical communication projects

Qualifications

Candidates must possess one of the following qualifications:
• Bachelor’s degree in Life Sciences
• Bachelor’s degree in Pharmacy
• Master’s degree in Life Sciences
• M Pharmacy
• Degree in Biotechnology or related healthcare discipline

Educational Requirements

• Full-time degree from a recognized university
• Strong academic background in medical, pharmaceutical, or life sciences
• Certification or training in medical writing will be an added advantage

Experience and Skills

Experience

• 1–3 years of experience in medical writing, clinical research, or regulatory documentation preferred
• Freshers with strong scientific writing skills may also be considered

Skills Required

• Excellent written and verbal communication skills
• Strong understanding of clinical research terminology
• Knowledge of ICH-GCP guidelines
• Ability to interpret clinical data and present it clearly
• Attention to detail and documentation accuracy
• Proficiency in MS Office tools
• Time management and ability to meet strict deadlines

Salary Insights

Offered Compensation

• ₹4,00,000 per annum (CTC)
Additional Benefits:
• Exposure to global clinical documentation standards
• Skill enhancement in regulatory and scientific writing
• Opportunity to work on diverse therapeutic areas
• Professional growth within CRO environment

Company Overview

Croissance Clinical Research is a Clinical Research Organization providing end-to-end research support services to pharmaceutical, biotechnology, and healthcare companies. CROs play a vital role in managing clinical trials, regulatory documentation, and scientific communication.
Working with a CRO offers structured exposure to international regulatory standards, sponsor interactions, and compliance-driven documentation processes.

FAQs

1. Is prior medical writing experience mandatory?
   Experience is preferred, but strong scientific writing skills are essential.

2. Location of posting?
   Hyderabad.

3. What type of documents will be handled?
   Clinical study documents, regulatory submissions, and scientific reports.

4. Growth opportunities?
   Experience in this role can lead to Senior Medical Writer or Regulatory Writing roles.

Application Tips

• Revise basics of clinical research and ICH-GCP guidelines
• Prepare writing samples if available
• Highlight documentation or research experience in resume
• Demonstrate strong grammar and technical writing ability
• Be prepared to discuss previous projects or research work