Responsibilities:

• Assist in the development of medical content, including clinical study reports, regulatory documents, and scientific manuscripts.
• Conduct thorough research on assigned topics and gather relevant information from credible sources.
• Collaborate with cross-functional teams to ensure accuracy and compliance with regulatory guidelines.
• Learn and adapt to different writing styles and formats as per project requirements.
• Participate in training sessions and workshops to enhance writing skills and domain knowledge.

If you are passionate about medical writing and meet the above qualifications, we encourage you to apply by sending your resume to hr@syconcro.com