- Developing and executing the medical affairs strategy for the therapy portfolio, including clinical trial design, publication planning, and medical education.
- Building and maintaining relationships with external stakeholders, such as healthcare professionals, patient advocacy groups, and regulatory agencies.
- Supporting the launch of new products by providing medical expertise and ensuring appropriate labeling and communication of safety and efficacy data.
- Providing medical support to cross-functional teams, such as marketing, sales, and regulatory affairs, to ensure alignment and consistency in messaging and strategy.
- Contributing to the development of scientific publications, including abstracts, posters, and manuscripts, to disseminate clinical trial data and other relevant information.
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