Responsibilities This is an exciting opportunity to join a highly engaged team of passionate oncology infusion nurses who embody work-life balance! Seeking an enthusiastic, flexible, team-oriented individual with strong communication and...
Whether you are healthy, or have a specific illness, we'll connect you with the right trial. Potentially get paid to access the most cutting edge medicines combating your disease. Most trials don't require much effort and will be located near...
Title: Assistant Research Nurse Administrator - CCTOLocation: Upper East SideOrg Unit: NursingWork Days: Monday-FridayWeekly Hours: 35.00Exemption Status: ExemptSalary Range: $132,700.00 - $147,500.00*As required under NYC Human Rights Law Int...
The Associate Medical Director works with their supervisor and other members of the cross-functional study team to author protocols and facilitate execution of study activities and data summarization. Takes lead on collaborations with discovery...
If you are physically/mentally ill or healthy, get paid to trial new treatments and medications.This is a great way to earn additional income, sometimes from the comfort of your home.Participation in clinical trials can be a very rewarding...
Department/Unit: SCC Operating Room Work Shift: Day (United States of America) Hourly Range: $33 Albany Med South Clinical Campus is seeking Operating Room nurse. New Graduate Nurses encouraged to...
Job Description Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Essential...
The Department of Health is currently seeking a Public Health Nurse I within our Maternal Health group at our Great River location. Under general supervision, an employee in this class performs public health nursing services for...
Job Summary:A Clinical Research Associate I will have a detailed understanding of each study protocol and background knowledge of the study medication and therapeutic area under study; will determine subject population availability and list and...
Overview Responsible for pre-clinical trial set up, initial and ongoing regulatory submission and IRB activities, subject screening and enrollment, specimen collection and transmittal, data collection and management, adverse...