Engage in scientific dialog with healthcare system National Thought Leaders and collaborate with colleagues on capturing medical insights. Provide strategic input into materials for national medical congresses and facilitate partnerships and research collaborations. Focus on Cardiovascular area.

Lead and manage clinical trials, ensuring execution aligns with strategy, budget, and timelines. Author and review clinical trial documents and SOPs. Oversee CRO activities and manage trial-related issues, ensuring regulatory compliance. Your expertise in clinical trial management will be critical in accelerating our mission.

The Clinical Project Manager is responsible for operational aspects of planning, implementation, execution, and management of one or more clinical research studies, ensuring clinical trial is completed within established timelines and of the highest quality. Oversee management of CROs, and third-party vendors. Proactively evaluates study risks.

Provide exceptional care to the patients of Moore County as a clinical staff pharmacist within our inpatient pharmacy. Rotate through the main pharmacy and decentralized settings, participate in multi-disciplinary rounds in critical care, initiate and monitor pharmacokinetic processes, and support antibiotic selection. The position allows for occasional remote workdays.

The main function of this role will be triaging calls and assisting callers. Contact physician’s office as needed for refill authorization. Contact client for verification of orders as needed. Process all new and refill prescriptions, verify eligibility, proof and input prescriptions while maintaining productivity and quality standards.

As a Sr. Project Manager, you will lead and manage the tactical execution of one or more clinical studies from study startup through database release and drive decision making to provide input to operational strategy. You will also provide quality oversight to the Contract Research Organisation (CRO) and of the CRO deliverables related to study execution.

The Gene Therapy Guide is a regional field-based position that help support patient/caregivers at every step of the treatment journey regarding access, reimbursement, and logistics. The Guide will work closely with Qualified Treatment Centers, physicians, genetic counselors, nurses, pharmacists, and ancillary staff, as well as patients and caregivers of patients to onboard and address barriers to patient access.

The Director, Patient Engagement will play a critical role in the success of clinical trials by ensuring identification, engagement, and retention of the right patients. This position requires a strategic thinker with a deep understanding of patient recruitment and retention methodologies. The Director will lead the development and execution of patient-centric strategies.

The Medical Science Liaison (MSL) identifies and engages with national and regional thought leaders/healthcare professionals (HCPs), payers, and managed care accounts. This role delivers educational and compliant scientific information in support of Karyopharm’s pipeline, serving as Karyopharm’s scientific representative to the medical community.

The Associate Director, Clinical Operations plays a key role in the execution of clinical trials, ensuring operational excellence and successful delivery. This position involves overseeing the day-to-day management of clinical trials and collaborating with cross-functional teams. The role ensures adherence to the highest standards of quality and compliance, contributing to advancing innovative mental health therapies.