About the role#
This internship focuses on biosample management and precision medicine execution. You will work with our team from June 2027 through May 2028. The schedule is full-time at 37.5 hours per week during the summer and 20 hours per week for the remainder of the term.
What you'll do#
- Review clinical study informed consent forms at the master, country, and site levels.
- Use an Excel template to log permitted uses for biosamples and data.
- Summarize study findings in PowerPoint presentations.
- Create an FAQ document to help the team design future informed consent forms.
- Present your findings to stakeholders to explain differences in data and biosample usage across countries.
- Support the review and approval process for tissue return requests.
What you'll need#
- Current enrollment in an undergraduate or graduate program in biology, biomedical sciences, pharmaceutical sciences, or a related field.
- Proficiency in Excel.
- Strong organizational and communication skills.
- Ability to handle multiple tasks and meet deadlines.
- Interest in clinical trials.
- Prior experience in a corporate business environment is preferred, and experience in the pharmaceutical industry is a plus.
Location & details#
- This position is based on-site in Basking Ridge, New Jersey.
- This is a paid internship.
About Daiichi Sankyo Japan
Daiichi Sankyo Japan operates as a pharmaceutical manufacturer based in Tokyo. The company focuses on the research, development, and sales of medical products. It specializes in treatments for cancer and cardiovascular diseases. The organization employs over 10,000 people and was founded in 2005.
How to get in at Daiichi Sankyo Japan
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