Regulatory Submissions Jobs in Princeton, NJ
Regulatory Submissions Jobs in Princeton, NJ

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Associate Director, Edt Documentation Lead, Early Development
At Bristol Myers Squibb we are inspired by a single vision transforming patients lives through oncology hematology immunology and cardiovascular disease and one of the most diverse and promising pipelines in the industry each of our passionate colleagues contribute to innovations More...
General SummaryUnder limited supervision develops analyzes reports and interprets complex financial information to assist management in evaluating and executing the organizations business plans in compliance with the Health Services Cost Review Commission (HSCRC) and Center for Medica More...
Director Global Regulatory Strategy And Policy Advisor - Job Id Grspa
DescriptionAscendis Pharma is a dynamic fastgrowing global biopharmaceutical company with locations in Denmark Europe and the United States. Today were advancing programs in Endocrinology Rare Disease and Oncology.Here at Ascendis we pride ourselves on exceptional science visionary le More...
About This Role:As a Medical Director Clinical Development Immunology you will be an integral member of the Immunology Therapeutic Area within the Clinical Development Organization. In this dynamic role you will play a critical part in shaping and advancing clinical programs particula More...
Changing lives. Building Careers.Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us change equals opportunity. Every day our colleagues are challenging whats possible and making headway to More...
Responsibilities: Develop test and validate SAS programs to generate analysis datasets (ADaM) TLFs and adhoc reports. Ensure datasets and outputs adhere to CDISC standards and regulatory guidelines (e.g. FDA EMA). Collaborate with Biostatisticians Data Management and Clinical Teams More...
Working with UsChallenging. Meaningful. Lifechanging. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the lat More...
The Role:This role will support Oncology Therapeutic programs specifically supporting the Clinical Development Lead in the direction and evaluation of Phase 13 clinical studies. The principal responsibility for this role is ensuring the comprehensive data quality of clinical studies More...
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