Intern, Clinical Operations
About The Position
Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously. Location: Foster City, in-office | Duration: 8-12 weeks Mirum Pharmaceuticals is a growing rare-disease biopharmaceutical company focused on transforming the lives of patients with cholestatic liver diseases. Mirum is advancing several programs globally, including volixibat, LIVMARLI® (maralixibat), MRM-3379 and BJT-778 in different rare diseases. We are offering a unique opportunity for a motivated, analytical, and scientifically curious individual to join our Global Clinical Operations Team in Foster City, CA. This short-term internship will contribute to ongoing clinical programs and strategic evidence generation supporting Mirum’s next-generation therapies in rare diseases. The selected intern will work closely with Clinical Operations to review study related document and the trial master file to ensure completeness and accuracy. Additionally, the selected individual will work closely with the clinical operation’s lead to review data listings, create trackers and manage samples to ensure completeness and accuracy. During this internship you will contribute meaningfully to data interpretation, data review and evidence generation activities working alongside an agile and passionate team that values curiosity, precision, and impact. Let’s learn, get things done, and have fun seriously!
Requirements
- Currently enrolled at an accredited college/university in a Bachelor’s degree in biological sciences or related health related field.
- Demonstrated analytical rigor and ability to interpret complex data sets.
- Fluency in English required
Nice To Haves
- Excellent written and verbal communication skills, including scientific writing.
- Comfortable working closely with your Mentor and also independently in a cross-cultural, matrix environment.
- Highly motivated to learn and grow!
Responsibilities
- Review study-related documents and Trial Master File (TMF) contents to ensure completeness, accuracy, and regulatory compliance
- Assisting in the review, distributing, and archiving of study specific documents and reports (plans, training materials, study guides, manuals etc.).
- Collaborate with Clinical Operations leads to review data listings for consistency, quality, and completeness
- Develop and maintain tracking tools (e.g., study trackers, dashboards) to monitor study progress and document status
- Support sample management activities, including tracking, reconciliation, and documentation of clinical samples
- Communicate with cross-functional teams to resolve discrepancies and ensure timely completion of clinical study deliverables
- Assisting in the preparation of meeting materials, scheduling meetings, for internal clinical operation team meetings.
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What This Job Offers
Career Level
Intern
Number of Employees
101-250 employees
