Hi All Medical Writers. I have this remote contract role with my client who is a Biopharmaceutical company. Candidates "MUST HAVE ALL OF THE FOLLOWING SKILLS". Interested candidates email me to [click apply] They hired one contractor so I know what they are looking for. Anyone qualified and interested?
- Advanced degree (PhD, PharmD, MD, or MSc) in Life Sciences, Medicine, Pharmacy, or a related field
- Minimum 3-5 years of medical writing experience in the pharmaceutical, biotech, or CRO industry
- Strong background in writing regulatory documents for clinical trials and submissions
- Ability to simplify complex scientific concepts for diverse audiences
Proficiency in ICH guidelines, GCP, and regulatory submission requirements (FDA, EMA, etc.)
- Strong attention to detail, ability to manage multiple projects, and meet deadlines
- Ability to work independently and collaboratively in a fast-paced environment
- High level of Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
- Experience with document management systems and publishing tools (e.g., EndNote, Adobe Acrobat, regulatory submission platforms)
- Veeva experience