Medical Writer
Homebased / remote working
Publicada en: 26/04/2024
Tipo de empleo: Indefinido
Sector: Farmacéutica y Asistencia sanitaria
Responsibilities:
- Write high-quality medical documents, such as clinical trial protocols, study reports, summaries, and informed consent.
- Ensure scientific accuracy, clarity, and consistency of all medical content.
- Comply with relevant regulatory guidelines, such as Good Clinical Practices (GCP) and ICH guidelines.
- Collaborate with a multidisciplinary team of researchers, physicians, and other healthcare professionals.
- Stay up-to-date on the latest research and regulations in the field of clinical trials.
- Perform other tasks as needed.
Qualifications:
- Bachelor's degree in a life science, such as medicine, pharmacy, nursing, or biology.
- Prior experience in writing medical documents. ( submission).
- Strong understanding of regulatory guidelines, such as GCP and ICH guidelines.
- Excellent writing and editing skills in English.
- Ability to work independently and as part of a team.
- Detail-oriented and meticulous.
- Ability to meet tight deadlines.
Contact
Carlos Álvarez
+34 91 787 93 00
Morgan Philips Executive Search
Paseo de la Castellana 141, 17º
28046 Madrid
España
MS Word, PDF, HTML y formatos de texto