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Go to next pageHydrogen Group - Hoboken, NJ, United States, 07030
The Medical Writing consultant will act as primary contact for medical writing projects. Some typical job duties include:
- Collaborating with the clinical & regulatory teams to write clinical documents for regulatory submissions, including but not limited to:
- NDA's
- CSR's
- Safety Evaluation Reports
- Medical literature analysis reports
Qualifications:
- 5 years Regulatory Writing experience
- Demonstrated experience in the development of regulatory/ clinical submissions (preferably as a medical writer for pharmaceutical industry)
Desired Qualifications:
- Advanced degree (Ph.D, MD, Sc.D, MA/MS or MPH). Experience as author or contributor of peer-reviewed manuscripts is strongly desired.
- Strong verbal, written, and interpersonal communication skills.
- Highly proficient in using Microsoft Office applications (Word, Excel, PowerPoint) and EndNote.
- Therapeutic experience in CNS (Alzheimers and Narcolepsy)
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Writing/Editing
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Hydrogen Group is hiring: Medical Writer Consultant in Hoboken
