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Job Requirements of Biosample Management Operations Intern:
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Employment Type:
Full-Time
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Location:
Basking Ridge, NJ (Hybrid)
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Biosample Management Operations Intern
At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society.
Job Summary
We are currently seeking a Biosample Management Operations Intern from June 2026 – May 2027. This position will be full-time (37.5 hours) in the summer and part-time (20 hours) for the remainder of the internship.
Job Description
The intern will assist with biorepository operations, vendor oversight, data accuracy verification, and informed consent governance, while collaborating with cross-functional teams including Biosample Management, Precision Medicine, Clinical Study Teams, and Procurement. This role provides hands-on exposure to biorepository processes, compliance requirements, and cross-functional collaboration in clinical development.
Responsibilities
- Assist in managing long-term storage (LTS) at the biorepository and overseeing the coordination of sample movements needed for LTS or post-study analysis
Provide vendor performance/oversight responsibilities for the Biorepository (e.g. KPI management and oversight, issue escalation, etc.)
Support the verification of data accuracy at the Biorepository including specimen identifiers and metadata, and ICF-associated permissions prior to utilization.
Collaborate with Procurement to review contracts and ensure qualification for biorepository vendors responsible for long-term storage.
Assist the Biorepository Lead and Head of BSM as needed to manage the communication with Precision Medicine and the clinical study teams to address informed consent and IRB/EC questions related to biosamples in long-term storage in the biorepository
Ensure that samples are tracked, stored, destroyed, and used appropriately in line with the associated Informed Consent Forms and associated SOPs
Qualifications
Currently pursuing a degree in Life Sciences, Biotechnology, Pharmacy, Pharmaceuticals, or a related field.
Basic understanding of drug development process, informed consent and biorepository.
Strong organizational skills with attention to details and ability to prioritize competing timelines.
Good communication skills and ability to collaborate effectively with internal and external teams.
Proficiency in Microsoft Office applications.
Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.
Salary Range:
USD$17.23 - USD$58.15