met for specimen procurement, proper collection, processing and shipment of specimens. Serves as Primary Research Coordinator...Major Responsibilities: Performs clinical and administrative coordination of sponsored clinical trials, research...
Purpose Perform the day-to-day administrative activities of the clinical research trials program. Provide support... consent from program participants. Conduct or coordinate training for program participants. Coordinate research protocols...
center of everything we do at the Medical College of Wisconsin (MCW). As an Research Grants Coordinator, you will Develop... while maintaining federal and state compliance laws. Areas of oversight will include research involving human subjects, laboratory...
Purpose Perform the day-to-day administrative activities of the clinical research trials program. Provide support... consent from program participants. Conduct or coordinate training for program participants. Coordinate research protocols...
Clinical Research Coordinator III/Regulatory Specialist-IRB Purpose Responsible for gathering regulatory documents... budgets. Primary Functions – Clinical Research Coordinator III - Oversee the recruitment, screening, enrolling...
Summary Perform the day-to-day administrative activities of the clinical research trials program. Provide support... Assist senior research nurses and CRCs on data entry for ongoing studies. Recruit, screen, enroll and obtain consent...
Summary Perform the day-to-day administrative activities of the clinical research trials program. Provide support... and obtain consent from program participants. Conduct or coordinate training for program participants. Coordinate research...
Summary Perform the day-to-day administrative activities of the clinical research trials program. Provide support... Responsibilities Assist senior research nurses and CRCs on data entry for ongoing studies. Recruit, screen, enroll and obtain...
Summary Perform the day-to-day administrative activities of clinical research trial programs. Provide support to the... participants. Coordinate research protocols including arranging necessary appointments and procedures, working collaboratively...
Details Department: Research Oncology Schedule: Full Time, Days Hospital: CSM Hospital Location: Milwaukee, WI... of the offer. Responsibilities Coordinate administrative and clinical aspects of multiple research projects. Collaborate...
Purpose Perform the day-to-day administrative activities of the clinical research trials program. Provide support.... Coordinate research protocols including arranging necessary appointments and procedures, working collaboratively...
Summary Perform the day-to-day administrative activities of the clinical research trials program. Provide support... and obtain consent from program participants. Conduct or coordinate training for program participants. Coordinate research...
Summary Perform the day-to-day administrative activities of clinical research trial programs. Provide support to the.... Conduct or coordinate training for program participants. Coordinate research protocols including arranging necessary...
Summary Perform the day-to-day administrative activities of the clinical research trials program in Neurosciences.... Coordinate research protocols including arranging necessary appointments and procedures, working collaboratively...
center of everything we do at the Medical College of Wisconsin (MCW). In the role of a CTO Disease Team Research Manager... on Early Phase (Phase I, First in Human) trials for Solid Tumor types. Will be a catalyst for clinical research initiatives...
Licensure. ONS preferred and Certified Clinical Research Coordinator (ACRP) or Certified Clinical Research Professional (SoCRA...The Medical College of Wisconsin (MCW) brings a synergy between the best medical education, research and patient care...
) and other databases as appropriate under the direction of the research nurse or study coordinator. Under the direct guidance, assist...Purpose Under general supervision, assist in various administrative and data collection aspects of clinical research...
Summary Under general supervision, assist in various administrative and data collection aspects of clinical research..., and distribute to appropriate location Collect required data from study coordinators and research nurses, and enter onto clinical...
Major Responsibilities: Works with the Research Compliance Analyst II in providing review of post approval materials... (modifications, significant new information, unanticipated problems, noncompliance reports). Works with IRB coordinator to route...
. Primary Responsibilities Under the direction of the Manager of Clinical Research, study coordinator, research nurse...Summary Assist clinical research staff by providing administrative and data collection support for clinical studies...