Senior Regulatory Submissions Lead, Clinical Trials

Bristol Myers Squibb is seeking a Senior Specialist in Submission Management Clinical Trials for their facility in Poland, Województwo mazowieckie. This role involves supporting regulatory activities for clinical trials, ensuring compliance with global standards, and collaborating with stakeholders to define submission strategies. The ideal candidate will have a BA/BS degree in a science/technology field and over 3 years of related experience. The position offers competitive compensation ranging from zł174,980 to zł212,026, along with various employee benefits. #J-18808-Ljbffr