This role involves managing and facilitating the structure, formatting, and publication of various regulatory documents such as clinical study reports, investigator brochures, and safety aggregate reports. Responsibilities include partnering with internal and external authors, providing guidance on submission readiness, assisting with report-level content planning, remediating Word files, and contributing to the compilation of regulatory documents.
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biopharmaNew York, NY, US
Learn more about Wendy Short Bartie, Executive Vice President, Corporate Affairs, is responsible for advancing our company strategy through strategic communications, corporate social responsibility, corporate marketing and brand reputation, and patient advocacy.
Who they serve
Bristol Myers Squibb's medicines are for patients with serious diseases.