Daiichi Sankyo, Inc.
Biosample Management Intern
Daiichi Sankyo, Inc., Basking Ridge, New Jersey, us, 07920
Join a Legacy of Innovation 125 Years and Counting!
Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 125 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 18,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people. In addition to a strong portfolio of medicines for cardiovascular diseases, under the Group’s 2025 Vision to become a “Global Pharma Innovator with Competitive Advantage in Oncology,” Daiichi Sankyo is primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.
We are currently seeking a Precision Medicine Intern for a year (June 2025 – May 2026). This full time or position works for approximately 37.5 hours per week.
Responsibilities:
-Review clinical study informed consent forms (Master, country and site level) and capture key information in an existing excel file template regarding the permitted uses of biosamples and data (training to be provided on key information to capture) -Summarize the key findings from each clinical study in powerpoint slides and in an ICF FAQs document used by the Biosample Management team to design informed consent forms for future studies -Present the findings to relevant stakeholders to highlight some of the differences in permitted biosample and data use from various countries
Education/Experience: Interest in learning more about clinical trials Ability to extrapolate key information from complex documents Experience with Excel required Excellent organizational and communication skills Ability to manage multiple competing priorities and meet timelines
Qualified candidates must currently be enrolled in an accredited undergraduate or graduate program with a concentration in science or related field. Prior experience in a corporate business environment is preferred; experience in the pharmaceutical industry is a plus.
Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer.
All 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.
Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 125 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 18,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people. In addition to a strong portfolio of medicines for cardiovascular diseases, under the Group’s 2025 Vision to become a “Global Pharma Innovator with Competitive Advantage in Oncology,” Daiichi Sankyo is primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.
We are currently seeking a Precision Medicine Intern for a year (June 2025 – May 2026). This full time or position works for approximately 37.5 hours per week.
Responsibilities:
-Review clinical study informed consent forms (Master, country and site level) and capture key information in an existing excel file template regarding the permitted uses of biosamples and data (training to be provided on key information to capture) -Summarize the key findings from each clinical study in powerpoint slides and in an ICF FAQs document used by the Biosample Management team to design informed consent forms for future studies -Present the findings to relevant stakeholders to highlight some of the differences in permitted biosample and data use from various countries
Education/Experience: Interest in learning more about clinical trials Ability to extrapolate key information from complex documents Experience with Excel required Excellent organizational and communication skills Ability to manage multiple competing priorities and meet timelines
Qualified candidates must currently be enrolled in an accredited undergraduate or graduate program with a concentration in science or related field. Prior experience in a corporate business environment is preferred; experience in the pharmaceutical industry is a plus.
Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer.
All 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.