UPMC Cancer Centers   Location:   UPMC Cancer Centers, one of the largest integrated community networks of cancer physicians and health care specialists in the country, allows patients to receive the highest level of cancer care without having to leave their communities. Working with the University of Pittsburgh Cancer Institute, UPMC Cancer Centers is able to offer patients the latest advances in cancer prevention, detection, diagnosis and treatment at locations throughout the tristate region.
				Full/Part Time:
									Full-Time
				Regular/Temporary:
									Regular

Job Summary
	UPMC Cancer Centers, located in the Shadyside area of the city of Pittsburgh, is hiring a Research Associate, to work full-time, to help support the PCI-CRS Administration HF Department.Under the direction of the Program Manager, the research associate will work with physicians, nurses and allied health professionals to facilitate clinical research trials provided through the University of Pittsburgh Cancer Institute (UPCI) and UPMC Cancer Centers and to independently execute job functions related to protocol management.
	Responsibilities
	Assists in verifying subject eligibility according to protocols by reviewing medical records, laboratory, and radiology or CT scan results. Assists in the coordination of initiation, site evaluation, monitoring visits, and audits required by the sponsor. Shares responsibility of managing the day to day activities for the research protocols. Process required documents as need for the research protocols. Will serve as an assistant to support all main functions of the department. Insures that patient¿s records, slides, radiology tests, lab work results, etc. are obtained and reviewed prior to patient entry into a study. Performs consenting process and study implementation of lab, registry, and non-therapeutic clinical trials. Create study specific source documents, case report forms and study visit checklists. Responsible for prompt and accurate data collection for protocols. Assists in entering subject trial registration and study status updates into CTMA.
	Basic Qualifications
	High school diploma or equivalent required. Bachelor's degree in healthcare or related field OR four years of experience in clinical research and/or related setting OR three years of experience in clinical research with certification Additional skills include prior knowledge and use of Microsoft Office software produces and the ability to work with a PC database applications. Preferred knowledge of reach mythology and prior supervisory and or/ project management experience preferred.
	Licensure/Certifications

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Number of Openings:	1
Requisition Number:	14-7859
Job Title:	Clinical Research Assistant
Department:	39537-Child Health, Behavior & Devel
City:	Seattle
State:	Washington
Location:	West 8th
Secondary Location:
Union:	None
Work Status:	Regular
Shift:	Day Shift
FTE/Hours per pay period:	1.0 FTE (80 hours per bi-weekly pay periods)
Hours Per Shift:
Call Hours:
Work Days:	Monday-Friday
Salary:	Depends on Experience
Job Description:	Assist and provide administrative support for assigned Division research team with specific aspects of the organization, implementation and completion of clinical research trials. Coordinate the recruitment, enrollment and scheduling of study participants. Track regulatory documents and correspondence, maintain study files, collect and enter data and maintain databases, and assist the PI or Clinical Study Manager in the general implementation of clinical studies.
Requirements:	Required: - High School Diploma or equivalent - Two (2) years of college-level coursework in biological or life sciences or health related field - At least one (1) year of work experience Preferred: - Bachelors Degree in biological or life sciences or health related field - At least three (3) years in a research or health care setting - Familiarity with US Food & Drug Administration (FDA) regulations and International Conference on - Harmonization (ICH) and Good Clinical Practice (GCP) guidelines - Knowledge of medical terminology

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The Children's Hospital of Philadelphia is an equal opportunity employer. We do not discriminate on the basis of race, color, gender, gender identity, sexual orientation, age, religion, national or ethnic origin, disability or protected veteran status.

Requisition #:Job Title:City:State:Scheduled Shift:Employee Type:*Scheduled Days:Research Division:Requirements:Job Description: 14-32932 Clinical Research Assistant I Philadelphia Pennsylvania Days Regular - Full Time Monday through Friday Saturday Sunday CHILD DEVELOPMENT Bachelor’s degree in Psychology, Social Work, Education, Public Health or related field; Prior clinical research experience and experience in urban schools and communities much preferred.All CHOP employees who work in a patient building or who provide patient care are required to receive an annual influenza vaccine unless they are granted a medical or religious exemption. Works across several grant-funded research studies related to aggression/bullying and violence prevention. CRA I will participate in an array of clinical and applied research activities including working with MA-level facilitator to conduct group interventions, qualitative data collection activities, or other school-based interventions. Research activities will include recruitment, informed consent procedures, participant tracking, pre/post-intervention data collection, data entry and checking, and quantitative and qualitative data analysis. CRA I will also prepare study materials and protocols, and assist in manuscript and grant writing. To accomplish these tasks, CRA I will receive weekly supervision from licensed psychologist and will participate in regular research team meetings with PI, Co-I, Program Manager, Coordinator, and study team members across multiple projects to gain a better understanding of protocol issues, study goals and timelines, and project developments

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Job ID	7943BR
Job Title	Research Assistant
Location	MD - Rockville
Career Area	Research
Job Status	Full-Time
Job Description	We are seeking a research assistant to work as part of a small team on several evaluations in the areas of homelessness, public health, global nutrition, and vulnerable populations, among others. Responsibilities will include working on the development of both qualitative and quantitative data collection tools, collecting data as part of site visit teams, preparing data for analysis (both qualitative and quantitative), conducting preliminary data analyses (using both quantitative software and statistical packages), graphically representing data findings, and assisting in the writing of reports and articles. A bachelor’s degree in social science is required. Any offer of employment will be contingent upon receipt of acceptable results from a background screening based on the specific position which will include, at a minimum, criminal records history. Westat is an Equal Opportunity Employer and does not discriminate on the basis of race, creed, color, religion, sex, age, national origin, veteran status, disability, or any other classification protected by Federal, state, or local law.

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