Pharmaceutical Documentation Specialist

5 days ago


Pretoria, Gauteng, South Africa MMS Holdings Inc Full time

About MMS Holdings Inc

We are a renowned CRO providing expert services in clinical trial data management and regulatory submissions.

Our team of professionals delivers high-quality results, ensuring compliance with rigorous regulatory standards.

We are seeking a highly skilled Medical Writer to join our South African team.

This home-based role offers the flexibility to work independently and manage projects with minimal supervision.

Key Responsibilities:
  • Review and analyze medical literature to identify relevant resources for clinical trials.
  • Develop and edit clinical development documents, including clinical protocols, investigator's brochures, and clinical study reports.
  • Meet deadlines and manage multiple writing assignments simultaneously.
  • Build strong relationships with clients and colleagues through exceptional communication skills.
  • Stay informed about industry trends and regulatory requirements.
Requirements:
  • Minimum 3 years of experience in the pharmaceutical industry.
  • Proven track record of successful regulatory writing and clinical medical writing experience.
  • Higher education in a scientific, medical, or clinical discipline.
  • Strong background in Oncology and clinical study protocol development.
  • Ability to lead projects and manage teams effectively.


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