Medical Content Writer

1. Develop highquality medical content including regulatory submissions clinical study reports scientific manuscripts and educational materials.
2. Conduct literature reviews and analyse data to support content development.
3. Ensure all content meets regulatory guidelines and industry standards.
4. Collaborate with crossfunctional teams including clinical research regulatory affairs and medical affairs.
5. Participate in the development of scientific communications plans and contribute to the strategic planning process.
6. Keep uptodate with emerging trends in medical writing and regulatory requirements.

1. Bachelors degree in life sciences or a related field required; advanced degree preferred.
2. Minimum of 3 years of experience in medical writing in the pharmaceutical biotech or medical device industry.
3. Strong knowledge of regulatory guidelines (e.g. FDA EMA ICH) clinical trial design and conduct and medical terminology.

1. Excellent written and verbal communication skills.
2. Ability to work collaboratively in a crossfunctional team environment.
3. Proficiency in Microsoft Office and other relevant software applications.
4. Demonstrated ability to manage multiple projects and deadlines.

1. 15K to 25K Per Month. Based on the experience with exponential opportunities for career growth.

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