As a leading Bio-Tech in the San Diego area, we are actively seeking a Medical Writing professional who has the aptitude to is become responsible for leading medical writing activities. Some responsibilities would include preparing preclinical regulatory documents, delivering strategy and execution for IND + NDA submissions, communicating time lines, preparing reports, and more.
As for basic requirements, the following should be met:
- Extensive work w/ documents including CSR's + IB's within Oncology
- IND + NDA
- Experience with Clinical Evaluation Reports
- Post Market Evaluation.
The firm has established an extremely modern culture by allowing for mixture of independent and collaborative working structures while allowing for extreme visibility as this function would report to executives of the business. They are also offering this role in a remote capacity.