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An exciting and innovative clinical-stage biopharmaceutical company dedicated to the development of first-in-class cellular immunotherapies for patients with cancer and autoimmune disease is looking for a Director of Medical/Technical Writing to join the Regulatory team and lead the company’s technical writing activities, including regulatory and clinical documents. This is a key role directly supporting the company’s development programs. The ideal candidate will have experience with a broad range of clinical and preclinical projects and documents, including clinical protocols, regulatory submissions, and scientific presentations. This is an exempt, full-time position located remotely with the expectation of traveling to corporate headquarters in San Diego, CA.
Responsibilities:
Qualifications:
Working Conditions and Physical Requirements:
The preceding job description indicates the general nature and level of work performed by employees within this classification. Additional and incidental duties related to the primary duties may be required from time to time.
Full Time
$177k-223k (estimate)
06/20/2024
07/09/2024
partnology.com
San Diego, CA