Medical Writer

Responsibilities:

• Write high-quality medical documents, such as clinical trial protocols, study reports, summaries, and informed consent.
• Ensure scientific accuracy, clarity, and consistency of all medical content.
• Comply with relevant regulatory guidelines, such as Good Clinical Practices (GCP) and ICH guidelines.
• Collaborate with a multidisciplinary team of researchers, physicians, and other healthcare professionals.
• Stay up-to-date on the latest research and regulations in the field of clinical trials.
• Perform other tasks as needed.

Qualifications:

• Bachelor's degree in a life science, such as medicine, pharmacy, nursing, or biology.
• Prior experience in writing medical documents. ( submission).
• Strong understanding of regulatory guidelines, such as GCP and ICH guidelines.
• Excellent writing and editing skills in English.
• Ability to work independently and as part of a team.
• Detail-oriented and meticulous.
• Ability to meet tight deadlines.