Regulatory Medical Content Specialist

5 days ago


Johannesburg, Gauteng, South Africa Syneos Health, Inc. Full time

At Syneos Health, we are dedicated to building a diverse, inclusive and authentic workplace. Our Clinical Development model brings the customer and the patient to the center of everything that we do.

Job Responsibilities
  • Mentors and leads less experienced medical writers on complex projects, as necessary.
  • Acts as lead for assigned writing projects.
  • Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision.
  • Develops or supports a variety of documents, including clinical study protocols, reports, and submissions.

Key qualifications include a strong understanding of English grammar, FDA and ICH regulations, and AMA style guide. Strong proficiency in Microsoft Office and ability to present complex information effectively.



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