Clinical Research Coordinator - Cancer Immunotherapy Program
UCSF Health, San Francisco, CA, United States
Job Description
The Helen Diller Family Comprehensive Cancer Center (HDFCCC) is seeking a Clinical Research Coordinator (CRC) to join the Cancer Immunotherapy Program within the Division of Hematology/Oncology. 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). 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
High school graduation and sufficient experience and demonstrated skills to perform assigned duties and responsibilities; and/or equivalent experience/training.
Attention to detail; strong interpersonal skills; excellent 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.
Demonstrated knowledge and understanding of research, especially in biological sciences.
Exceptional database management experience and prior experience with various computer programs (Microsoft Office; internet‑based databases) and using specialized software such as OnCore.
Experience with medical charts and electronic records.
Ability to sit and work at a computer for several hours per day; may need to travel between 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.
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 oncology patients.
Ability to work across several different programs, reporting to 2-3 different supervisors.
Preferred Qualifications
Bachelor’s degree with a major in science or related field.
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 into 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 and experience with Phase I–III trials.
Membership in a clinical research professional society.
Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, confidentiality and HIPAA 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 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.
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The Helen Diller Family Comprehensive Cancer Center (HDFCCC) is seeking a Clinical Research Coordinator (CRC) to join the Cancer Immunotherapy Program within the Division of Hematology/Oncology. 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). 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
High school graduation and sufficient experience and demonstrated skills to perform assigned duties and responsibilities; and/or equivalent experience/training.
Attention to detail; strong interpersonal skills; excellent 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.
Demonstrated knowledge and understanding of research, especially in biological sciences.
Exceptional database management experience and prior experience with various computer programs (Microsoft Office; internet‑based databases) and using specialized software such as OnCore.
Experience with medical charts and electronic records.
Ability to sit and work at a computer for several hours per day; may need to travel between 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.
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 oncology patients.
Ability to work across several different programs, reporting to 2-3 different supervisors.
Preferred Qualifications
Bachelor’s degree with a major in science or related field.
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 into 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 and experience with Phase I–III trials.
Membership in a clinical research professional society.
Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, confidentiality and HIPAA 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 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.
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