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Our research arm, Sarah Cannon Research Institute (SCRI), formed more than 20 years ago to ensure patients could access cutting-edge therapies closer to home.... - Indeed
One or more years of relevant experience as an SCRI clinical research professional (e.g., Clinical Project Associate, Research Monitor Associate, Clinical Data... - Indeed
2+ years of experience with research clinical trials. Summary of Key Responsibilities.... - Indeed
Scientifically review clinical research data including:. Minimum 3 years of experience in clinical research, experience in an academic medical center, or in the... - Indeed
Appreciation of clinical research and drug development process. Summary of Key Responsibilities:.... - Indeed
During employment with Sarah Cannon routine training requirements are assigned; This person will facilitate work across interdisciplinary workgroups in Sarah... - Indeed
Summary of Key Responsibilities: This position is responsible for clinical data management of SCRI clinical trials. This includes all data management - Indeed
Medical and clinical research terminology. Assist research staff in maintaining FDA compliance. Professional research certification required, SOCRA/ACRP... - Indeed
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