Medical Writer

Job Description:

Be responsible for writing and editing medical documents related to drug development and clinical trials. Collaborate with cross-functional teams to ensure the accuracy and compliance of the documents.

Key Responsibilities:

• Write and edit medical documents such as clinical trial protocols, study reports, informed consent forms, etc.
• Collaborate with medical experts, clinical research teams, and regulatory affairs teams to ensure the scientific accuracy and compliance of the documents.
• Ensure that the format and content of the documents meet company and industry standards.
• Participate in the review and revision process of documents to ensure their quality and consistency.
• Assist senior Medical Writers in project management and document archiving.

Qualifications:

• Bachelor's degree or above, preferably in medicine, pharmacy, biology, or related fields.
• Excellent English reading and writing skills, with the ability to proficiently write and edit English medical documents.
• Familiarity with GCP (Good Clinical Practice) and relevant regulatory requirements is preferred.
• Strong communication skills and a team-oriented spirit.
• Strong learning ability and adaptability, capable of working in a fast-paced environment.
• Prior relevant internship or work experience is preferred.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com