Job Description: Medical Writer

Responsibilities:

• Research, write, edit, and proofread a variety of medical and scientific documents including clinical study reports, regulatory submissions, manuscripts, abstracts, posters, and presentations.
• Ensure that all documents are accurate, clear, and adhere to regulatory guidelines and company standards.
• Collaborate with cross-functional teams to gather information and develop content.
• Interpret and present complex scientific data in a clear and concise manner for various audiences.
• Stay up-to-date on industry trends, guidelines, and best practices.

Skills:

• Excellent written and verbal communication skills.
• Strong attention to detail and accuracy.
• Ability to work independently and meet deadlines.
• Knowledge of medical terminology and scientific concepts.
• Proficiency in Microsoft Office and reference management software.
• Familiarity with regulatory requirements and guidelines (e.g., ICH, GCP).
• Experience with data analysis and interpretation.
• Strong organizational and project management skills.

Requirements:

• Bachelor's degree in a scientific discipline (e.g., biology, pharmacology, life sciences) or related field. Advanced degree (e.g., MS, PhD) preferred.
• Has 2 yeas Previous experience in medical writing within the pharmaceutical, biotechnology, or healthcare industry.
• Understanding of clinical research and drug development processes.

What you need to do now:

Click “Apply Now” if you are interested to be part of the team!

Alternatively, send your latest CV to Kalpana.charles@linksinternational.com for confidential discussion of your career!