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Research Scientist, Clinical Development

Job Location:

Princeton, NJ - USA

Monthly Salary: Not provided by the employer

Posted: 23 October 2026 (12 hours ago)

Application Deadline: 20 January 2027

Vacancies: 1 Vacancy

Responsibilities:

Reviews patient level and cumulative data per the data review plan across a study and coordinates with the medical lead for study level review
Reviews protocol deviations
Reviews safety data SAE reports (in collaboration with pharmacovigilance) labs efficacy data dosing data withdrawals/discontinuations
Collaborates with the medical lead to provide medical/scientific guidance during the execution of the study

Educational Requirements:

PhD PharmD or other related Advanced Medical Scientific Degree ( RN / BSN and MSN)
Experience in oncology.

Experience:

Minimum of 3 years combined experience in academic and/or industry oncology clinical research and drug development
At least 3 years in drug development industry in oncology and with previous exposure to clinical development regulatory and statistical activities such as e.g. (co-)authoring and reviewing of documents such as clinical trial protocols statistical analysis plans IND AR NDA AR PSUR DSUR IB ICF orphan drug designations regulatory briefing document etc. is preferable.
Ability to critically review and interpret Clinical data.
Working knowledge of the drug development process in the USA and EU is required.

Required Experience:

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