If you want to do something that matters, this work matters. Patients drive our passion to pioneer novel cancer therapies. That’s why we’ve built an environment centered around support, flexibility, and a shared mission. Creating and delivering medicine for cancer can only be done through focus, dedication, and heart. We hire exceptional people and trust each other to work in whatever way lets us, be us – whether that’s onsite, from home, or anywhere in between. 

Our summer intern program, which will run from May 27th – Aug 8th, allows students to gain real world work experience in a high energy, collaborative work culture.   

This intern will assist in QMS processes and systems administration to ensure consistent daily operations enabling GxP compliance and inspection-readiness. QMS administration processes include: Document Control, Deviations Management, Investigations Management, CAPA Management, Validation, Change Control, Risk Management, Training Management, Vendor Qualification, and GxP Auditing.

Under supervision of functional leads, intern will assist with day-to-day process/system administration and actively participate in QMS administration process improvement projects as assigned. Will interact with 5 functional leads and end users throughout the organization.

This internship will support continuous product supply for Karyopharm’s drug products (IMP) utilized in clinical trials.  The individual will work with the teams managing internal and external tasks and customers in order to accomplish project objectives and to understand the needs of the clinical trials. The Clinical Supply Chain Intern will support Clinical Supply Chain initiatives and continuous improvement activities.

Responsibilities

• Participate in cross-functional Project Team Meetings
• Partner with PM to review and understand the Clinical Supply study process
• Shadow the PM who coordinate and monitor label development process and packaging timelines with the vendors
• Learn how to process Temperature Excursions associated to study shipments through approval
• Organize and file various trial related documents
• Generate Quarterly Reports and the KPTI Performance and Risk Indicators.
• Oversight/participation of Clinical Trials processes

• Currently enrolled in a related Bachelor's degree program
• Must be highly organized and have the ability to work in independently and collaboratively as a team
• Clear, concise verbal & written communication
• Curious and willing to learn and use new tools / skills.
• Proficiency in Microsoft Word, Excel, PowerPoint, Teams & Zoom
• Familiarity with advanced Excel tools
• Familiarity with Process mapping
• You have a strong interest in life sciences and are passionate about giving patients with cancer a chance to enjoy more of life’s precious moments.  
• You feel a strong connection with our ICARE values (Innovation, Courage, Alignment & Accountability, Resilience, and Energy) 
• You demonstrate enthusiasm for learning and a commitment to career development

At Karyopharm, we live and demonstrate our ICARE values every day! Check out our Culture Video!