Pharmaceutical Documentation Specialist
5 days ago
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.
- 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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