Description

You will provide hands-on medical writing expertise and data review for preclinical and clinical stage projects.

Responsibilities

• Develop and manage clinical documents to ensure accuracy, consistency, and regulatory compliance.
• Manage writing assignments to meet strict project timelines.
• Lead technical discussions and address audit findings as a subject matter expert.
• Collaborate with internal teams across various project stages.

Required Skills

• Advanced scientific degree or equivalent graduate education.
• Minimum of 4-5 years in pharmaceutical regulatory writing.
• Deep understanding of drug development and clinical data.
• Experience with GCP, Clinical Trials, Regulatory Requirements, and NDA.
• Proficiency in MS Office and publishing software.
• Strong organizational and communication skills.

Preferred Skills

• Ability to manage cross-departmental relationships effectively.

Key Skills

Education

ANY GRADUATE