ApplyBlast uses AI to match you with the right jobs, tailor your resume and cover letter, and apply automatically so you can land your dream job faster.
© All Rights Reserved. ApplyBlast.com
ApplyBlast uses AI to match you with the right jobs, tailor your resume and cover letter, and apply automatically so you can land your dream job faster.
© All Rights Reserved. ApplyBlast.com
Tanabe Pharma America
This role involves preparing clinical documents, authoring scientific publications, evaluating investigative sites, presenting complex study data, and managing regulatory safety reporting within a pharmaceutical setting. The position requires scientific writing, understanding of regulatory standards, and collaboration across teams to support clinical trials.
Tanabe Pharma America (TPA) is a U.S. pharmaceutical company dedicated to developing treatments for serious, debilitating, and progressive diseases. Building on over 300 years of innovation, TPA conducts research and clinical development of specialty therapies, with a current pipeline including dersimelagon (MT-7117) for conditions such as Erythropoietic Protoporphyria. The company is committed to supporting patients and caregivers through community resources and partnerships with advocacy groups and healthcare providers.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for Tanabe Pharma America.
4% below the average for this role