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:
You have the ability to contribute towards every stage of the editorial development process, including content journey mapping, writing, regulatory review, and revisions. You are able to communicate in a clear and thorough manner with direct client contact, and internal reporting.
Pitch ideas for short- and long-form content. Qualifications Include: Three-plus years of experience working at a media company. Strong beat knowledge in personal computing and/or networking. The ability to write clearly and accessibly about complex topics.
Rahway, NewJersey, United States of America. North Wales, Pennsylvania, United States of America. Job Type Full Time. Job Description. Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation.
Research Communications and Medical Writer Lead. Description. Company Healthcare Research needs your communications and medical writing skills to help us tell a compelling story about healthcare today.