Clinical Research Coordinator - Pediatric Oncology/Hematology

General Information

Job Name Clinical Research Coordinator - Pediatric Oncology/Hematology Department 1431000 - M HDF Comprehensive Cancer Ctr Position type Full Time Workplace Fully On-Site Primary Location San Francisco, CA, United States Job ID CONV_88219BR

Description & Requirements

Job Description The Helen Diller Family Comprehensive Cancer Center (HDFCCC) is seeking a Clinical Research Coordinator to join the Pediatric Oncology/Hematology research team. The Clinical Research Coordinator will perform independently to execute, manage, and coordinate research protocols, as directed by the Clinical Research Manager and/or the Principal Investigator (PI), and/or the Associate Director for the Clinical Research Programs. The incumbent will coordinate the operations and data collection of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies. Qualifications Required Qualifications: - HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training. - Attention to detail; strong interpersonal skills; excellent, effective verbal and written communication skills to coordinate with subjects, team members, other departments and outside institutions; and the ability to multi-task in a fast-paced environment while working with a diverse subject population. - Ability to work well independently, complete projects in a timely manner, and prioritize multiple projects to ensure the completion of essential tasks by deadlines. Preferred Qualifications: - Fluency in the usage of Committee of Human Research (CHR) online iMEDris system for submission, renewal, and modification of protocols through this system. - Understanding of patient population to create rapport and a relationship, while also giving insight to what is realistic and appropriate for patient participation. - Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals - Experience with electronic medical records. - Prior analytical and writing skills in a science/research environment. - Knowledge of clinical research in oncology. - Knowledge and experience in managing oncology clinical trials. - Membership in a clinical research professional society. - Demonstrated knowledge and understanding of research, especially in the areas of biological sciences. - Prior experience with various computer programs (Microsoft Office; internet-based databases) and using specialized software such as OnCore. - Ability to sit and work at a computer for several hours per day. May need to travel between one or more campuses via UCSF shuttle. Ability to stand for several hours of the day. - Experience in clinical research or demonstrated research or training experience that translates into a clinical research setting. - Familiarity with specimen processing, or demonstrated ability to learn specimen processing in a laboratory environment. - Working knowledge of, or demonstrated ability to learn federal, state, and local research regulations and guidelines, and research practice methods in a laboratory or clinical setting. - Knowledge of medical terminology, and/or the ability to apply information to the assessment, interpretation, and processing of medical data. - Ability to independently interpret and apply policies, respond to requests, resolve issues, and provide assistance to faculty and staff at all levels in a team-oriented environment. - Ability to work with a sensitive population of patients (oncology patients). - Ability to work across several different programs, reporting to 2-3 different supervisors. - Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, confidentiality and HIPPA regulations, following the UCSF mission statement and purpose for research, and a clear understanding of policies and procedures on patient safety and confidentiality (electronic and hard copy medical records, patient charts, communication, etc.); knowledge of medical terminology, research policies and guidelines, guidelines for packing/shipping infectious substances, database building/analysis, and data management within some of the following: Access, Stata, SASS/ SPSS, and Teleform programming platforms. - Experience applying the following regulations and guidelines:- Good Clinical Practice Guidelines - Health Information and Accountability Act (HIPAA) - The Protection of Human Research Subjects - CHR regulations for recruitment and consent of research subjects - Effective Cash Handling Procedures - Environmental Health and Safety Training - Fire Safety Training

Additional Details

Job Code CLIN RSCH CRD (009335) Assignment Category Career IAP Level None Job Family Research and Laboratory Campus 1 Mission Bay (SF) Campus 2 Various Locations Campus 3 Mission Bay (SF) Percentage (%) 100 Shift Length 8 hours Shift Type Day Bargaining Unit RX Additional Shift Details Monday - Friday