Collaborates on and supports CTM on required tasks prior to commencement of clinical trials that include, but are not limited to clinical planning, protocol development, case report form CRF development, IRB submissions, investigator agreements,...
Required Qualification: (as evidenced by an attached resume) Associate's degree (foreign equivalent or higher). In lieu of a degree, two (2) years of full-time research related experience. Proficient with Microsoft Word, Excel, PowerPoint...
Imagine how your ideas and expertise can change a patient's life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how our products transform patients' lives. As part of our Clinical...
Bonuses and Benefits MVHS is offering up to a $1000 sign-on...
Schedule: Full time Availability: Morning, Afternoon, Evening (Includes Weekends). Age Requirement: Must be 18 years or older Location: Ithaca, NY Address: 500 S. Meadow Street Pay: $30 /...
**_Strength Through Diversity_** **_Ground breaking science. Advancing medicine. Healing made personal._** **_Roles & Responsibilities:_** The Clinical Research Coordinator is an entry human subjects researcher, responsible for...
Responsibilities Seeking a team focused professional with a passion for oncology. This is an exciting opportunity to join the Clinical Trials Office as part of the Wilmot Cancer Center (WCC) within the University of Rochester Medical Center...