Supports the research and treatment mission of Roswell Park and Clinical Research Services by managing the program study portfolio and coordinating the regulatory aspects of the studies assigned. Collaborates and communicates with investigators, sponsors and teams to assure research regulatory documentation is complete and the submission of new studies, amendments/modifications, continuing reviews and all other study documents are in accordance with the FDA Code of Federal Regulations (Title 21) and according to the guidelines set by the International Committee for Harmonization for Good Clinical Practices. The starting annual salary for this position is $62,877 and this can include a full comprehensive benefits package. The actual offer may vary based on qualifications, skills, and experience.
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Job Type
Full-time
Career Level
Entry Level
Number of Employees
1,001-5,000 employees