Senior Medical Writer
South Africa, Remote ID de la oferta R0000033398 Categoría Medical Writing Fecha de publicación 05/30/2025Overview
Como Redactor Médico en Parexel, sus sólidos conocimientos científicos, aptitudes para escribir y enfoque en el paciente comunican datos científicos complejos con eficacia a diversos interesados, incluidos organismos regulatorios, profesionales médicos y el público en general. Debe ser capaz de colaborar con equipos multidisciplinarios para desarrollar una amplia gama de documentos de investigación clínica, como formulario de consentimiento informado, reporte de estudio clínico, documentos de farmacovigilancia y más.
Fomentamos una cultura de inclusión, colaboración y aprendizaje continuo que empodera a nuestros empleados a ejercer un impacto positivo en las vidas de las personas.
Perfil del éxito
¿Posee estas competencias sociales y rasgos interpersonales para tener éxito en Parexel?
- Comunicador
- Adaptable
- Consistente
- Perspicaz
- Orientado al detalle
- Orientado al trabajo con plazos
Acerca de este rol
Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do. We believe in our values; Patients First, Quality, Respect, Empowerment & Accountability.
We are currently recruiting a Senior Medical Writer based in South Africa, who will work as part of the Drug Safety writing team.
The Senior Medical Writer is responsible for comprehensive signal management, including detection, analysis, and evaluation from various sources. They oversee the end-to-end signal management process, collaborate with client safety science , and adhere to client-defined plans and SOPs. The PMW also contributes to preparing, updating, and managing various safety documents including Risk Management Plans (RMPs), Periodic Safety Update Reports (PSURs), and other aggregate reports. This position requires expertise in pharmacovigilance processes and the ability to manage complex safety data.
This role also focuses on training junior staff, and requires strong communication, and problem-solving skills, balancing mentoring and client relation and requires expertise in pharmacovigilance, strong analytical skills, and the ability to collaborate across functions to ensure comprehensive product safety management across multiple therapeutic areas.
Knowledge and Experience:
- Relevant experience is desirable in Regulatory/ Pharmacovigilance or related field.
- Good knowledge of medical terminologies
Education:
- Science/Medicine degree: The minimum qualification required would be a university degree in life Sciences/Health or Biomedical Sciences (Pharmacy, microbiology, Biochemistry, Biotechnology, Biophysics etc.)
- A degree in Medicine/Dentistry/Physiotherapy/Experimental Medicine/Nursing, which involves patient exposure in hospital-based environment, would be an advantage
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POTENCIAL TRAYECTORIA PROFESIONAL
Parexel ofrece trayectorias profesionales para que los redactores médicos progresen en su puesto técnico o gerencial, además de opciones para transferirse a otras áreas del negocio.
- Redactor Médico Adjunto
- Redactor Médico I
- Redactor Médico II
- Redactor Médico Sénior
- Experto en la MateriaGestión de personal
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