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Karyopharm Therapeutics Inc. (the "Company") is an equal opportunity employer. All qualified applicants will be considered without regard to age, race, color, sex, religion/creed, national origin, marital status, ancestry, citizenship, military, reservist or veteran status, pregnancy, sexual orientation or preference, gender identity, gender expression, physical or mental disability, genetic predisposition or carrier status, or any other category protected under applicable federal, state or local law. Consistent with its obligations under applicable law, the Company will make reasonable accommodations for qualified individuals with disabilities. If you require an accommodation in the application process, please contact a member of the Company’s Human Resources department.
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TheSenior/Executive Director, Scientific Communications and Publications will be part of the Global Medical & Scientific Affairs (GMSA) leadership team and will be actively involved in strategy development to support Medical and cross-functional goals and objectives. This position will serve as a key collaborator with Global Medical Affairs for coordination of congress and publication planning. This position will also have external vendor oversight in managing the planning and execution of scientific communications and publications. To be successful, the Director, Scientific Communications and Publications must demonstrate business acumen and a strong ability to...
The Director, Global Medical Review, plays a key role in the GMSA Team and is responsible for ensuring medical and scientific accuracy of promotional and non-promotional materials in compliance with US laws and regulations and company policies. The position involves reviewing all materials submitted to the Medical Material Review Team (MMRT) and Commercial Review Committee (CRC) to ensure regulatory and scientific standards are met, while fostering collaboration with Legal and Regulatory teams to maintain compliance and quality. The Director, Medical Reviewer, is also responsible for reviewing all the social media...
The Senior Director of Quality Assurance will provide strategic and operational leadership for the quality
oversight of both drug substance and drug product manufacturing, packaging, labeling and distribution and
support Quality Management Systems within GMP operations . Manage activities and projects to meet
company objectives including review,...
The AD / Director is responsible for the development and implementation of regulatory strategies for specific projects, while serving as the regulatory lead on the respective program teams. He/she will also be the regulatory contact with relevant regulatory authorities, as appropriate. Reporting to Executive Director, Regulatory Affairs, you will positively impact patients’ lives by:
- Develop response and submission strategies to regulatory information requests in close...
The SVP of Clinical Development will be a key member of the CMO leadership team and will be responsible for asset and indication strategy, clinical trial strategy, execution, and analysis of all data. Along with this, the SVP of Clinical Development will support and build the clinical development team which includes medical leads, medical directors, and clinical research scientists who will be responsible for designing and monitoring assigned trials. This individual will work across the organization working with the PV, Regulatory, QA, Commercial, Medical Affairs, Business Development, Data management and Clinical Operations.
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The Medical Director will serve as the primary medical lead for Karyopharm study team within assigned clinical trials and with cross-functional teams on clinical trial strategy, design and execution. Along with this, the Medical Director will serve as the primary Medical Monitor responsible for monitoring the safety of enrolled subjects on assigned trials. This individual may work on multiple trials to include solid tumor(s), myeloma and other hematological studies.