Job Summary
A biopharmaceutical company is seeking a Remote Senior Informed Consent Writer.
Must be able to:
- Read and understand protocol-specific design
- Prepare study-specific informed consent documents
- Manage informed consent writing projects
Must meet the following requirements for consideration:
- Ability to travel 10%
- Bachelor's Degree in Life Sciences
- Competence in writing, editing and reviewing of informed consent documents
- Ability to prepare summary of a clinical trial design, objectives and activities for lay audience
- Technical expertise in Microsoft Office, Adobe Acrobat, document management systems
- Familiarity with SharePoint and concepts of structured content management