Kyowa Kirin is a global specialty pharmaceutical company backed by more than 70 years of breakthrough life science innovation, dedicated to discovering and advancing treatments for diseases in which unmet need is greatest. Based in Japan with worldwide operations, we work across the continuum from drug discovery to commercialization, guided by our commitment to patients and their families.
Our research teams, located in California and around the world, are focused on developing the next generation of antibody, cell, and gene therapies, with particular emphasis on bone and mineral disorders, hemato-oncology, and rare diseases. We accelerate development through collaborations with industry, academia, patients, and healthcare providers, and since 2018 we have introduced four new therapies serving patients with progressive illnesses often in need of new therapeutic alternatives.
Our culture is grounded in our values: Commitment to Life, Integrity, Innovation, and Teamwork/Wa, and brought to life through the Kabegoe Principles, which define the behaviors and actions that guide how we work together to deliver meaningful impact for patients.
We’re proud of the progress we’ve made and mindful of the countless individuals still waiting for their own breakthroughs. A commitment to making people smile unites our efforts. Learn more at www.kkna.kyowakirin.com.
Join the Clinical Operations team for a paid, hybrid summer internship offering hands‑on exposure to how clinical studies are planned, activated, monitored, and maintained. Working alongside subject matter experts in Trial Execution, the intern will contribute to active operational priorities while learning how clinical development teams collaborate to deliver high‑quality studies. The role includes preferred in‑office time and direct guidance from experienced Clinical Operations experts.
What You Will Learn:
By the end of the internship, you will understand how a clinical study progresses from planning and site activation through trial conduct and inspection readiness. You will build practical skills in essential document management, quality review, site support, issue tracking, process improvement, meeting documentation, and professional communication.
You will also gain experience working across functions and learn how Clinical Operations partners with study teams and other stakeholders to execute trials efficiently and in compliance with Good Clinical Practice.
Key Responsibilities:
Contribute to clinical trial execution activities with coaching and guidance from Clinical Operations team members, including:eTMF and Document Management Perform quality control checks on electronic Trial Master Files
Assist in compiling and reviewing essential document packets required to activate new clinical sites
Classify and tag uncategorized documents for audit preparedness
Provide support and become a key point of contact for contract and budget tracking related activities Site Management and Monitoring Support Assist the clinical trial execution team in monitoring trip report review
Assess site and master level Informed Consent documents to ensure compliance with company SOPs
Provide team assistance related to assigned Corrective Action Plans activities Process Improvement and Departmental Initiatives Optimize, maintain, and innovate trackers and tools utilized by the clinical operations team
Collate documents related to SOPs and training
Support ongoing initiatives to gather historical information on study specifics to develop a comprehensive and accurate database Develop a practical understanding of Good Clinical Practice, company procedures, and clinical operations standards, and learn how these requirements protect participants and support reliable trial execution.
Prepare clear and action-oriented department meeting minutes, capturing key decisions, owners, and follow-up activities.
Collaborate with cross-functional stakeholders to understand how Clinical Operations coordinates activities, resolves issues, and supports timely study delivery.
Requirements:
Must be currently enrolled in a Bachelor’s, Master’s, PharmD, or PhD degree program
Interns must be available to work from May 25, 2027 to August 20, 2027
Must be eligible to work in the United States without Sponsorship
A minimum GPA of 3.0 is required
The ability to work a hybrid schedule with three days on site is required
Prior internship or co‑op experience is preferred
Preferred fields of study include life sciences, health sciences, pharmaceutical sciences, healthcare administration, or a related discipline
Why Intern with Kyowa Kirin? Interning at Kyowa Kirin means joining a team that values curiosity, collaboration, and continuous learning. You’ll contribute to meaningful projects, receive mentorship from industry professionals, and experience a culture where every voice is welcomed and encouraged. If you’re looking for an internship where you can learn, grow, and make a real impact, we’d love to meet you.
The anticipated hourly rate for this position will be$23.00 to $33.00 per hour.
KKNA and all of its employees have an obligation to act in accordance with the law and with integrity in all our operations and interactions.
It is the policy of Kyowa Kirin North America, Inc. to provide equal employment opportunity to all qualified persons without regard to race, religion, creed, color, pregnancy, sex, age, national origin, disability, genetic trait or predisposition, veteran status, marital status, sexual orientation or affection preference or citizenship status or any other category protected by law.
Recruitment & Staffing Agencies Kyowa Kirin does not accept agency resumes unless contacted directly by internal Kyowa Kirin Talent Acquisition. Please do not forward resumes to Kyowa Kirin employees or any other company location; Kyowa Kirin is not responsible for any fees related to unsolicited resumes.
