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Ticker Symbol Entity Name Domain As Of Date Title URL Brand Category Location Text City State Country Posted Date Number of Openings Description Salary Salary Currency Salary Description Coordinates Date Added Date Updated Company Name Sector Industry
nasdaq:kpti careers-karyopharm.icims.com careers-karyopharm.icims.com Sep 9th, 2020 12:00AM Hematology/Oncology Specialist - San Francisco, CA Open San Francisco, CA Commercial San Francisco, CA, not set, USA CA San Francisco USA Jul 31st, 2020 12:00AM Job Locations US-CA-San Francisco Job Title Hematology/Oncology Specialist - San Francisco, CA The Hematology-Oncology Specialist maintains strong professional relationships in the patient care continuum and represents the integrity of Karyopharm Therapeutics by providing approved disease and product information and resources to key decision makers and stakeholders within the oncology community practice setting. - Develop business plans, market analysis, and strategy that link to strong business results and execute accordingly - Position on-label benefits for appropriate patients to key customer stakeholders to achieve or exceed forecasted sales goals - Resolve issues at account level to ensure access to therapy - Coordinate with colleagues in cross-functional areas including Market Access, Clinical Education, and Medical Affairs to facilitate customer and patient access to Karyopharm product(s) and information - Provide customer feedback to internal stakeholders, sharing best practices, unmet needs, and business opportunities - Assist Marketing function in identifying and inviting appropriate healthcare professionals (HCPs) to promotional and educational events or programs - Develop and maintain mastery of clinical and technical knowledge related to product(s) promoted, the oncology marketplace, and disease management - Foster and develop relationships with Key Opinion Leaders (KOLs), decision makers, influencers, and key stakeholders within the oncology community - Deliver clinical and technical value at medical meetings by staffing promotional booths, as requested - Comply with all laws and regulations and adhere to company compliance guidelines, policy and procedures - Acts with a sense of urgency on behalf of patients and customers   Job ID 2020-1600 Sep 9th, 2020 03:18PM Sep 9th, 2020 03:18PM Karyopharm Therapeutics Health Care Pharmaceuticals & Biotechnology
nasdaq:kpti careers-karyopharm.icims.com careers-karyopharm.icims.com Sep 9th, 2020 12:00AM Principal Clinical Research Associate - West Coast (remote) Open California Clinical Operations not set, CA, not set, USA CA not set USA Aug 12th, 2020 12:00AM Job Locations US-CA | US-CA | US-WA | US-CO | US-OR | US-NV | US-AZ Job Title Principal Clinical Research Associate - West Coast (remote) Oversees the progress of clinical investigations by conducting pre-study, initiation, interim and close out visits to sites.  Monitors clinical trials in accordance with Good Clinical Practices. Works closely with the Clinical Project Manager to ensure all monitoring activities are conducted according to study requirements. Please note this position can be remotely based throughout the US.      RESPONSIBILITIES: - Participates in the investigator recruitment process. Performs initial qualification visits of potential investigators. Evaluates the capability of the site to successfully manage and conduct the clinical study, both clinically and technically. - Assists in the preparation and review of protocols, eCRFs, study manuals, and other study documents as requested. - Obtains and reviews regulatory documentation for successful implementation, monitoring, and evaluation of clinical trials including submission if required - Performs study initiation activities; reviewing with the site personnel the protocol, regulatory issues, study procedures, and provides training on completion of the eCRF. - Conducts periodic site file audits to ensure compliance with GCPs and accuracy of Trial Master File aAssures adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures through on-site monitoring visits. Prepares monitoring reports and letters in a timely manner in accordance with the study monitoring plan. - Performs investigational product inventory. Verifies destruction of unused materials or ensures return to designated location, as required. - Reviews the quality and integrity of the clinical data through (1) in house review of electronic CRF data and (2) on-site source verification. Works with sites to resolve data queries. - Serves as primary contact between Karyopharm and investigator Participates in study team meetings providing monitoring updates. - Assists with, attends, and may present at Investigator Meetings for assigned studies. - Performs study close-out visits. - May request site audits for reasons of validity. - Performs other duties as requested. - Up to 75% domestic travel Job ID 2020-1588 Sep 9th, 2020 03:18PM Sep 9th, 2020 03:18PM Karyopharm Therapeutics Health Care Pharmaceuticals & Biotechnology
nasdaq:kpti careers-karyopharm.icims.com careers-karyopharm.icims.com Sep 9th, 2020 12:00AM Senior Clinical Research Associate - Central US Open *Karyopharm Therapeutics Inc (Hdqtrs.) Clinical Operations Newton, MA, 02459, USA MA Newton USA Sep 3rd, 2020 12:00AM Job Locations US-MA-Newton | US-TX | US-CO | US-MO | US-IL | US-MI | US-Remote Job Title Senior Clinical Research Associate - Central US Oversees the progress of clinical investigations by conducting pre-study, initiation, interim and close out visits to sites.  Monitors clinical trials in accordance with Good Clinical Practices. Works closely with the Clinical Project Manager to ensure all monitoring activities are conducted according to study requirements. Please note this position can be remotely based throughout the US.  Up to 75% domestic travel may be required after travel resritctions have been relaxed. Our team currently works remotely.      RESPONSIBILITIES: - Participates in the investigator recruitment process. Performs initial qualification visits of potential investigators. Evaluates the capability of the site to successfully manage and conduct the clinical study, both clinically and technically. - Assists in the preparation and review of protocols, eCRFs, study manuals, and other study documents as requested. - Obtains and reviews regulatory documentation for successful implementation, monitoring, and evaluation of clinical trials including submission if required - Performs study initiation activities; reviewing with the site personnel the protocol, regulatory issues, study procedures, and provides training on completion of the eCRF. - Conducts periodic site file audits to ensure compliance with GCPs and accuracy of Trial Master File aAssures adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures through on-site monitoring visits. Prepares monitoring reports and letters in a timely manner in accordance with the study monitoring plan. - Performs investigational product inventory. Verifies destruction of unused materials or ensures return to designated location, as required. - Reviews the quality and integrity of the clinical data through (1) in house review of electronic CRF data and (2) on-site source verification. Works with sites to resolve data queries. - Serves as primary contact between Karyopharm and investigator Participates in study team meetings providing monitoring updates. - Assists with, attends, and may present at Investigator Meetings for assigned studies. - Performs study close-out visits. - May request site audits for reasons of validity. - Performs other duties as requested. - Up to 75% domestic travel Job ID 2020-1590 Sep 9th, 2020 03:18PM Sep 9th, 2020 03:18PM Karyopharm Therapeutics Health Care Pharmaceuticals & Biotechnology
nasdaq:kpti careers-karyopharm.icims.com careers-karyopharm.icims.com Sep 10th, 2020 12:00AM Senior Vice President, Strategy and Portfolio Management Open *Karyopharm Therapeutics Inc (Hdqtrs.) Research and Development Newton, MA, 02459, USA MA Newton USA Aug 10th, 2020 12:00AM Job Locations US-MA-Newton Job Title Senior Vice President, Strategy and Portfolio Management    SUMMARY: The SVP, Strategy and Portfolio Management, will be responsible for providing strategic and analytic leadership across all areas of R&D pipeline strategy and management including identifying asset-level, research/early stage portfolio interactions and implications as well as highlighting gaps and making recommendations. The VP, Strategy and Management will provide pipeline and strategic expertise to all members of the R&D senior leadership team. Additionally, The SVP, Strategy and Portfolio Management will lead and manage a team of Program Leaders.   RESPONSIBILITIES: - The SVP, Strategy and Portfolio Management, will provide high level oversight, management and drive across the span of development from strategy formulation to execution of that strategy; this encompasses the entire process from preclinical research through registration.  - The Strategy and Portfolio Management team will coordinate between all internal/external stakeholders (e.g. Clin Ops, Medical, Pre-clinical, PIs, MSLs, Regulatory, Research, Drug supply, Publications as well as Investigators, Patient groups) to ensure alignment, operational efficiency and program success. - Creates and supports a consistent, linked strategic framework across early and late stage assets to enable strategic decision-making—including strategic context setting, decision structuring, risk assessment, value profiles, governance preparation, etc. - Provides direction on product development requirements to meet expectations of external customers and business stakeholders. Interacts with research and development, marketing, manufacturing, and regulatory departments and with external stakeholders. - Provides strategic leadership and expertise with respect to decision making--providing real-time evaluation and identification of material events, critical analysis of problems and utilization of insights.   - Monitors pipeline progress and industry benchmarking data, identifies trends, risks and gaps and recommends specific strategies to enhance/optimize KPTI’s pipeline.  Drives pipeline review events, processes and deliberations including scenario planning and trade-off decisions - Partners directly with governance members and senior leaders to ensure preparation, implementation and follow-up of scientific and pipeline-related decisions and actions. - Drives synchronization and harmonization of inputs, outputs and processes across R&D governance and other pipeline related forums with a goal of streamlining and enhancing stakeholder experience associated with the pipeline governance and evaluation/management process. Specific responsibilities include chairing of forums, agenda curation and executive communications. - Responsible for project performance, risk management, administration, financial management and issue resolution for functional group Job ID 2020-1604 Sep 10th, 2020 02:53AM Sep 10th, 2020 02:53AM Karyopharm Therapeutics Health Care Pharmaceuticals & Biotechnology
nasdaq:kpti careers-karyopharm.icims.com careers-karyopharm.icims.com Sep 10th, 2020 12:00AM Senior Director, Senior Compliance Counsel (Remote) Open *Karyopharm Therapeutics Inc (Hdqtrs.) General & Administrative Newton, MA, 02459, USA MA Newton USA Aug 25th, 2020 12:00AM Job Locations US-MA-Newton | US-CA | US-CO | US-FL | US-NJ | US-NY | US-NC | US-DC | US-TX | US-Remote Job Title Senior Director, Senior Compliance Counsel (Remote) We are looking for an experienced attorney to join us as Senior Director, Senior Compliance Counsel. This position will report to the Chief Compliance Officer.  This role will be remote, however the successful candidate will need to have the ability to travel to our headquarters in Newton, MA as required. The Senior Director, Senior Compliance Counsel will serve as the legal reviewer for advertising and promotional materials as well as materials used by Global Medical Affairs.  This role will serve as a legal subject matter expert across areas of healthcare regulatory law and product liability.  Maintaining a focus on the external environment, the Senior Director, Senior Compliance Counsel will track and communicate to the organization significant decisions, legislation and regulatory rulings that may affect the company. Additionally, this role will serve as a compliance business partner, providing proactive compliance guidance and support across key functions within the business.  This role will assist in the development and implementation of compliance training and initiatives.  This role will have high visibility throughout the organization, supporting core business activities and cross functional teams as assigned.  The successful candidate in this role will develop strong and positive working relationships with colleagues at all levels.  This role will also lead and support a variety of cross functional projects as assigned.   Responsibilities: - Legal Reviewer for Promotional Advertising Review Team - Legal Reviewer for Medical Materials Review Team - Legal advisor in areas of healthcare regulatory law, fraud and abuse laws, privacy laws and other areas as assigned. - Compliance business partner supporting key business functions - Cross functional project participation and/or leadership - Compliance program support (e.g. training, monitoring, policies) - Other tasks as assigned.   -   Job ID 2020-1601 Sep 10th, 2020 02:53AM Sep 10th, 2020 02:53AM Karyopharm Therapeutics Health Care Pharmaceuticals & Biotechnology
nasdaq:kpti careers-karyopharm.icims.com careers-karyopharm.icims.com Sep 10th, 2020 12:00AM Senior Vice President, Medical Sciences Open *Karyopharm Therapeutics Inc (Hdqtrs.) Research and Development Newton, MA, 02459, USA MA Newton USA Aug 25th, 2020 12:00AM Job Locations US-MA-Newton Job Title Senior Vice President, Medical Sciences SUMMARY: The SVP- Medical Sciences will serve as the primary medical lead for developing the strategy for development of Karyopharm assets across indications with cross-functional study teams on clinical trial strategy, design and execution. Along with this, the SVP- Medical Sciences will support and build medical team/medical directors responsible for monitoring the assigned trials. This individual will work across the organization working with the PV, Regulatory, QA, Commercial, Medical Affairs and Clinical Operations. This RESPONSIBILITIES - Provide strategic input to portfolio management and prioritization - Serve as the key partner and contributor for the strategic planning, support early and translational development; and prepare specific strategic plans and initiatives. - Closely collaborate with the Medical Director and Scientists in the development of new strategic options for assets in late development. - Participates in the development of Study Protocols, Investigator's Brochures, Clinical Development Plans and other key study documents in conjunction with other line functions and with minimal guidance. - Serves on cross-functional teams for assigned trials, working with other team members to achieve efficient, high-quality study execution. - Participates in the preparation of regulatory documents in support of regulatory submissions, including clinical section of IND’s and CTA’s, IND safety reports and annual reports for assigned trials, responses to regulatory authorities and Ethics Committees/IRBs, and other documents as appropriate. - Provides scientific and clinical input to study-related documents and analysis plans including Informed consent forms (ICF), clinical research forms (CRF), statistical analysis plans (SAP), clinical pharmacology analysis plans (CPAP), and clinical study reports (CSR). - Acts as liaison between Clinical Development and other internal groups at Karyopharm (e.g., Regulatory Affairs, Clinical Operations, Clinical Data Management) for assigned studies. - Develop and execute life-cycle management plan, lead data generation activities such as medical affairs studies to unmet medical needs and data gaps - Support Medical Affairs: Working with field medical, Scientific Communication and Publication, Medical Information and Communication teams and provide support including reactive material development to address external stakeholder questions - Help identify and effectively interact with thought leaders to engage in scientific and medical exchange as well as understand unmet medical needs and data gaps - Support IST Program - Partner with pharmacovigilance to assess the safety profile of compounds - Maintain a high level of clinical and scientific expertise in the disease area(s) by reviewing the literature, attending medical/scientific meetings, and through personal interchanges with consultants, thought leaders, investigators and internal stakeholder. - Author manuscripts and collaborate with cross-functional colleagues and thought leaders to meet publication plan objectives - Maintain ethical standards of the highest level and have the knowledge and ability to comply with all relevant ethical, regulatory, and legal standards - May participate in or lead clinical development contributions to due diligence or other business development activity - As required by program needs, contribute in partnership with Discovery colleagues to the design and implementation of translational strategies - Supports clinical study teams, monitoring overall study integrity, and review, interpretation, and communication of accumulating data pertaining to safety and efficacy of the molecule - Present at scientific, medical and regulatory meetings globally - Develop and maintain relationships with academic investigators, pharmaceutical partners/sponsors, KOL’s, and patient advocacy groups - Contribute to activities in support of the company’s planned NDA submissions. Author clinical sections for INDs, NDAs, and other related documents   Job ID 2020-1593 Sep 10th, 2020 02:53AM Sep 10th, 2020 02:53AM Karyopharm Therapeutics Health Care Pharmaceuticals & Biotechnology
nasdaq:kpti careers-karyopharm.icims.com careers-karyopharm.icims.com Sep 10th, 2020 12:00AM PV Associate Open *Karyopharm Therapeutics Inc (Hdqtrs.) Research and Development Newton, MA, 02459, USA MA Newton USA Aug 26th, 2020 12:00AM Job Locations US-MA-Newton Job Title PV Associate The Pharmacovigilance (PV) Associate responsibilities include, but are not limited to, performing the intake of safety information received by Karyopharm PV, reviewing and processing the safety information in accordance with department procedures, and distribution of Individual Case Safety Reports (ICSRs) to appropriate destinations. The PV Associate will support other case management and clinical trial activities as needed.  - Perform data entry in Karyopharms Argus Safety Database, including duplicate check, new case creation, and ICSR generation/distribution and participate in workflow management to ensure adherence to case processing timelines - Support of Case Owners and Lead Specialists in case processing activities such as data entry - Monitor possible sources of safety information, and review and process safety information in a timely, thorough, and accurate manner - Utilize multiple spreadsheets to track incoming safety information - Independently formulate and complete follow up information reporters - Notify applicable parties regarding receipt of safety information - Communicate with vendors and/or business partners regarding the exchange of ICSRs - Reconcile safety information received by Karyopharm PV. - Ensure regulatory compliance with timelines for individual expedited case report submissions and provide assistance and timely delivery of information for aggregate reports, ad hoc report compilations, and other regulatory documents, as requested - Assist in review of department procedures and participate as needed in procedure revisions - All other Adhoc assignments as required Job ID 2020-1617 Sep 10th, 2020 02:53AM Sep 10th, 2020 02:53AM Karyopharm Therapeutics Health Care Pharmaceuticals & Biotechnology
nasdaq:kpti careers-karyopharm.icims.com careers-karyopharm.icims.com Sep 10th, 2020 12:00AM Senior Director, Commercial Innovation Open *Karyopharm Therapeutics Inc (Hdqtrs.) Commercial Newton, MA, 02459, USA MA Newton USA Sep 2nd, 2020 12:00AM Job Locations US-MA-Newton | US-Remote | US-NY | US-NJ | US-NC | US-DC | US-FL | US-GA | US-IL | US-TX | US-CO | ... Job Title Senior Director, Commercial Innovation Reporting to the Chief Commercial Officer, this role will be responsible for driving innovation across the Commercial organization by partnering internally across field-based, local and functional teams as well as with external stakeholders.  The Senior Director, Commercial Innovation will lead the development & execution of an experimentation framework driving innovation & agile optimization for the brands as well as infusing a test & learn culture across the organization.  - Enhance the commercial value offering, including but not limited to digital innovation, enhanced HCP engagement strategy, patient value, and value-based care - Identify opportunities with strong potential for commercial and/or patient value creation, and design and execute pilots to strategically disrupt the market and differentiate Karyopharm offerings - Drive new ways of doing things and experimentation to drive growth against new targets, sales channels and customer segments - Lead a test-and-learn approach to commercial innovation, including rapid prototyping, testing, designing and scaling leading-edge customer experiences - Set the innovation agenda and assist the CCO to define innovation priorities - Provide deep knowledge and expertise on the competitive global market and customer engagement trends to commercial and other functional partners - Develop an assessment framework for pilots to evaluate impact and predict future success - Facilitate workshops and discussions to generate, evaluate and prioritize ideas and scope innovation projects, in order to establish clear priorities for maximum business throughput - Monitor pilots against expectations and make recommendations to kill early, improve or scale - Develop business cases and, working closely with cross-functional partners, implement plans to scale pilots and embed into existing commercial team Job ID 2020-1619 Sep 10th, 2020 02:53AM Sep 10th, 2020 02:53AM Karyopharm Therapeutics Health Care Pharmaceuticals & Biotechnology
nasdaq:kpti careers-karyopharm.icims.com careers-karyopharm.icims.com Sep 11th, 2020 12:00AM Principal Clinical Research Associate - West Coast (remote) Open California Clinical Operations not set, CA, not set, USA CA not set USA Aug 12th, 2020 12:00AM Job Locations US-CA | US-CA | US-WA | US-CO | US-OR | US-NV | US-AZ Job Title Principal Clinical Research Associate - West Coast (remote) Oversees the progress of clinical investigations by conducting pre-study, initiation, interim and close out visits to sites.  Monitors clinical trials in accordance with Good Clinical Practices. Works closely with the Clinical Project Manager to ensure all monitoring activities are conducted according to study requirements. Please note this position can be remotely based throughout the US.      RESPONSIBILITIES: - Participates in the investigator recruitment process. Performs initial qualification visits of potential investigators. Evaluates the capability of the site to successfully manage and conduct the clinical study, both clinically and technically. - Assists in the preparation and review of protocols, eCRFs, study manuals, and other study documents as requested. - Obtains and reviews regulatory documentation for successful implementation, monitoring, and evaluation of clinical trials including submission if required - Performs study initiation activities; reviewing with the site personnel the protocol, regulatory issues, study procedures, and provides training on completion of the eCRF. - Conducts periodic site file audits to ensure compliance with GCPs and accuracy of Trial Master File aAssures adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures through on-site monitoring visits. Prepares monitoring reports and letters in a timely manner in accordance with the study monitoring plan. - Performs investigational product inventory. Verifies destruction of unused materials or ensures return to designated location, as required. - Reviews the quality and integrity of the clinical data through (1) in house review of electronic CRF data and (2) on-site source verification. Works with sites to resolve data queries. - Serves as primary contact between Karyopharm and investigator Participates in study team meetings providing monitoring updates. - Assists with, attends, and may present at Investigator Meetings for assigned studies. - Performs study close-out visits. - May request site audits for reasons of validity. - Performs other duties as requested. - Up to 75% domestic travel Job ID 2020-1588 Sep 11th, 2020 02:39AM Sep 11th, 2020 02:39AM Karyopharm Therapeutics Health Care Pharmaceuticals & Biotechnology
nasdaq:kpti careers-karyopharm.icims.com careers-karyopharm.icims.com Sep 25th, 2020 12:00AM Medical Director/Senior Medical Director, Pharmacovigilance Open *Karyopharm Therapeutics Inc (Hdqtrs.) Research and Development Newton, MA, 02459, USA MA Newton USA Sep 22nd, 2020 12:00AM Job Locations US-MA-Newton Job Title Medical Director/Senior Medical Director, Pharmacovigilance The Medical Director/Senior Medical Director, Pharmacovigilance (PV) will provide broad support of activities requiring medical safety input for assigned products, pre- and post-approval. He/she will support and/or lead periodic safety signaling reviews and meetings, as well as perform individual and aggregate case review. He/she will also participate, in varying degrees, on clinical teams/programs and other intra and/or inter-departmental activities and initiatives.   - Represent department as medical safety lead on cross-functional study and program teams for assigned products and studies, providing expert guidance regarding safety matters and issues. - Provide timely and sound medical review of individual case safety reports from clinical trials or post-marketing sources as needed. - Participate in protocol development, specifically the monitoring and collection of safety information in clinical trial protocols, as well as statistical analysis plans. - Participate in the analysis of safety data from on-going and completed clinical trials and representation in Clinical Study Reports. - Lead preparation and review of periodic reports (IND, Annual Safety, DSUR, PBRERs, CSR). - Review and provide medical content, as needed, for key study-related documents, e.g. IB, ICF, IDMC Charter. - Participate in departmental development activities including SOP and Work Instructions development. - Provide guidance to staff regarding optimal practice regarding collection, evaluation and processing of adverse experience reports, from a medical perspective. - Provide a contributory role in Partner /Affiliate agreements and interactions, as needed. - As directed by the PV Head, assume primary responsibility/chair for the conduct of one or more Safety Team(s) for assigned products. - Lead the regular review of safety data for assigned products for the identification of new safety signals, in accordance with signal detection practices. - Provide Risk Management Strategy. - Other activities, as needed or as requested by manager. Job ID 2020-1603 Sep 25th, 2020 05:57AM Sep 25th, 2020 05:57AM Karyopharm Therapeutics Health Care Pharmaceuticals & Biotechnology

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