Clinical Research Coordinator – Hematology/Oncology (Santa Barbara) | UCLA

Santa Barbara, California, Description TheClinical Research Coordinator supports the operational management of clinicalresearch activities throughout the study lifecycle, including design, start-up,conduct, and closeout. This role is responsible for implementing and managingresearch activities for one or more studies, prioritizing tasks to meetrequired deadlines. The Coordinator plans and organizes study activities to ensurecompliance with study protocols and applicable regulations, includinginstitutional policies, FDA Code of Federal Regulations (CFR), and ICH GoodClinical Practice (GCP). The role involves close collaboration with thePrincipal Investigator, ancillary departments, central research teams, sponsors,and external institutions to support compliant study conduct, financialmanagement, and adequate staffing. Hourly Salary Range: $36.37 – $58.52 Qualifications Required: Bachelors Degree or 1-3 years of previousstudy coordination or clinical research coordination experience Strong verbal and written communication skillsalong with strong interpersonal skills to effectively establish rapport, andbuild collaborate relationships. Strong organizational capabilities to organizemultiple projects and competing deadlines for efficiency andcost-effectiveness. Working knowledge of the clinical researchregulatory framework and institutional requirements. Analytical skillssufficient to work and solve address problems and identify solutions withreasoned judgment. Ability to adapt to changing job demands andpriorities; work flexible hours to accommodate research deadlines. Ability to respond to situations in anappropriate and professional manner. Ability to concentrate and focus in a workenvironment that contains distracting stimuli and competing deadlines. Ability to be flexible in handling workdelegated by more than one individual. Typing and computer skill/ability includingword-processing, use of spreadsheets, email, data entry. Ability to navigatenumerous software programs and applications. Ability to handle confidential materialinformation with judgement and discretion. Mathematical skills Sufficient to prepareclinical research budgets, knowledge of math ability and knowledge of clinicaltrials research budgeting process to assist with the preparation of clinicaltrial budgets. Working knowledge of FDA Code of FederalRegulations (CFR) and ICH Good Clinical Practice (GC) for clinical research. Be available to work in more than oneenvironment, travel to meetings, off-site visits, conferences, etc.