Arrowhead Pharmaceuticals -
The Position: Arrowhead is seeking an experienced Regulatory/Medical Writer to join its Regulatory Affairs team. The Regulatory/Medical Writer will work collaboratively with Arrowhead's regulatory ...
SoftPros - 4 days ago
Caravel Group Communications -
The Senior Medical Writer is responsible for the accuracy of the content development from ... A clear understanding of the regulations governing the biotechnology and pharmaceutical industries
LinkedIn - 4 days ago
South San Francisco
The Associate Director of Medical Writing will focus on protocol development, CSRs, IBs, and regulatory submissions. The successful candidate will work closely with cross-functional teams to ensure ...
Jobble, Inc. - 3 days ago
Apollomics, Inc. -
Primary Duties and Responsibilities • With input from other team members (Clinical, Development Operations, Biostatistics, Regulatory Affairs, Drug Safety, Pre-Clinical), the Medical Writer ...
Neuvoo - 9 days ago
The Director, Medical Writing will be responsible for writing various clinical and regulatory documents including distributing work with contractors or agencies as needed. The position's focus ...
SoftPros - 10 days ago
Amazon Corporate LLC -
... and regulations. Placement is contingent on Amazon's ability to apply for and obtain an export ... medical device manufacturing, software development * 5+ years of experience with business or ...
Monster - 10 days ago