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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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The Medical Science Liaison (MSL) is responsible for the identification and engagement of a targeted group of national and regional thought leaders/healthcare professionals (HCPs), as well as payers and managed care accounts. This position provides consistent delivery of educational and compliant scientific information in support of Karyopharm’s pipeline.
RESPONSIBILITIES:
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Responsible for supporting the Clinical Project Manager (CPM) with operational aspects of planning, implementation, management and tracking of the clinical trial activities and ensuring clinical trial deliverables are completed per established timelines and of the highest quality. Responsible for study start-up activities. Direct management of CROs and other third-party vendors including proactively identifying any upcoming issues or risks to study deliverable and escalating to CPM and study team. Maintenance of Trial Master File throughout the study lifecycle to ensure inspection readiness and...
Karyopharm is looking to hire an energetic, entrepreneurial, and resourceful Executive Assistant to support multiple C level executives. This position will play a key role within the organization as we aim to improve the lives of patients with cancer. We are seeking a candidate who is highly organized, relentlessly dedicated, and has knack for identifying problems before they happen.
This will be a hybrid working arrangement with the opportunity to work a flexible schedule remotely and onsite.
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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.
Join our team as a Regulatory Affairs Manager and play a pivotal role in shaping the success of our global regulatory strategies. In this position, you will lead critical regulatory submissions, drive agency interactions, and ensure compliance with evolving regulatory standards. From managing labeling initiatives and regulatory intelligence projects to co-chairing cross-functional subteams, you will be at the forefront of...
The Senior MSL is an experienced oncology professional with scientific, clinical, and therapeutic area expertise responsible for providing medical expertise on all the Karyopharm assets in development. This individual is a highly valuable member of the Global Medical and Scientific (GMSA) team who represents Karyopharm externally by engaging in highly credible scientific discussions with targeted Key Opinion Leaders (KOLs), internal stakeholders, clinical trial investigators, access stakeholders and other healthcare professionals to help support the medical objectives at Karyopharm. We are looking for someone who approaches the role with thoughtful consideration of the future.
We are seeking an experienced and detail-oriented regulatory affairs professional to join our team as a Director of Regulatory Submissions. This critical role will oversee the planning, management, and execution of regulatory submissions, ensuring high-quality dossiers that meet global regulatory standards. Acting as a strategic partner and conduit between cross-functional teams, this individual will streamline submission processes and drive continuous improvement in tools, templates, and SOPs. With a focus on collaboration and excellence, this role is pivotal in ensuring timely, accurate submissions that align with organizational objectives and regulatory requirements