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Clinical Research Coordinator II - Heme Onc

Req # 33286 Job Location Los Angeles, California - US
The Clinical Research Coordinator II serves as clinical research project manager on several additional externally-funded research projects in Hematology Oncology. The coordinator will contribute to the design of research projects to meet proposal goals established by the PI and sponsor. They will perform statistical data analysis and reporting functions as assigned. Insure project milestones are met, manage compliance issues and serve as liaison with project sponsors, P.I.’s, support staff, study participants, and professional journal editors.

Qualifications: BA, BS or AA in Health related field, Masters preferred; transferable experience in related field, with preference given to experience in Hematology Oncology. Minimum Experience Required: Three years medical clinical trials experience.

Knowledge, Skills and Abilities Required: Familiarity with Phase I,II, III and pharmaceutical Clinical Trials. Thorough knowledge of one or more database application programs. Excellent verbal and written communication skills. Good organizational skills. Ability to work under pressure and meet deadlines; work independently; pay attention to detail Skills: Experience in computerized database maintenance, study design coordination. Statistical analysis experience preferred. Strong oral and written communication skills required for patient education, study subject enrollment, multi-disciplinary appointment coordination, and active participation in study team meetings. Ability to work with complete independence as well as to collaborate with other professional team members and support staff.

License, Registration or Certification Required: Clinical Research Certification through SOCRA; ACRP, or obtained within 6 months of employment. 
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