- KBR (Washington, DC)
- Title: Principal Specialist / Protocol Officer KBR's Product and Technology Solutions Division specializes in rapid prototyping and advanced technology solutions ... is seeking a motivated, highly organized, and experienced Principal Specialist / Protocol Officer to join our team in...academic institutions and foreign governments. + Coordinate with NRL event hosts to provide support necessary to ensure that… more
- Merck (Rahway, NJ)
- …and the operational/executional arms within the business. Working independently, the Protocol Clinical Supplies Project Manager ( Protocol CSPM) designs strategic ... for authoring the Clinical Supplies section of the study protocol as well as preparation and presentation of the...our company. No fee will be paid in the event a candidate is hired by our company as… more
- University of Miami (Miami, FL)
- …patient data for Investigator review to determine patient eligibility for protocol enrollment.14. Maintains screening, enrollment, adverse event , deviation, ... opportunity for a Full Time Hybrid Clinical Research Data Specialist to work at the UHealth Medical campus in...registration and submission of data, monitoring compliance with the protocol , adherence to SOPs, and all applicable regulations and… more
- University of Miami (Miami, FL)
- …patient data for Investigator review to determine patient eligibility for protocol enrollment. + Maintains screening, enrollment, adverse event , deviation, ... has an exciting opportunity for a (Temp/Part-Time) Clinical Research Data Specialist position. The incumbent assists in enrolling subjects along with creating,… more
- University of Miami (Miami, FL)
- …for protocol enrollment. + Maintain s screening, enrollment, adverse event , deviation, tumor measurement, concomitant medication, delegation an d other sponsor ... of SCCC has an exciting opportunity for a Full Time Clinical Research Data Specialist to work hybrid at the UHealth medical campus in Miami, Fl. The Clinical… more
- University of Miami (Miami, FL)
- …patient data for Investigator review to determine patient eligibility for protocol enrollment.14. Maintains screening, enrollment, adverse event , deviation, ... opportunity for a Full Time Hybrid Clinical Research Data Specialist to work at the UHealth Medical Campus in...registration and submission of data, monitoring compliance with the protocol , adherence to SOPs, and all applicable regulations and… more
- University of Miami (Miami, FL)
- …patient data for Investigator review to determine patient eligibility for protocol enrollment. Maintains screening, enrollment, adverse event , deviation, tumor ... of SCCC has an exciting opportunity for a Full Time Clinical Research Data Specialist to work at UHealth Medical Campus in Miami, FL 33136. The Clinical Research… more
- J&J Family of Companies (Santa Clara, CA)
- …AE reporting + Assists in training of study personnel regarding the adverse event definitions per protocol + Collaborates on additional Clinical Affair's ... **Job Description:** Johnson & Johnson is hiring for a **Principal Clinical Safety Specialist - Shockwave Reducer** to join our team. The position is **FULLY REMOTE**… more
- DMS International (Virginia Beach, VA)
- …mandatory drug screenings. DMS is currently seeking an Administrative Management Specialist . The Administrative Management Specialist will independently deliver ... an activity with eighteen (18) training locations. The Administrative Management Specialist works closely with other contractor, military, and government civilian… more
- Weill Cornell Medical College (New York, NY)
- Title: Research Nurse Specialist Location: Upper East Side Org Unit: Nursing Work Days: Monday-Friday Weekly Hours: 35.00 Exemption Status: Exempt Salary Range: ... role when Hired for NYC Offices **Position Summary** The Research Nurse Specialist performs a variety of technical and administrative duties concerning specific… more