University of California, San Francisco
Clinical Research Coordinator
University of California, San Francisco, San Francisco, California, United States, 94199
Clinical Research Coordinator
University of California, San Francisco — Helen Diller Family Comprehensive Cancer Center Job Summary
The Clinical Research Coordinator (CRC) will independently or with general direction at the fully operational level execute, manage, and coordinate research protocols under the direction of the Lead Clinical Research Coordinator, Principal Investigator (PI), and/or the Research Personnel Manager for the Investigational Trials Unit. This includes coordination of multiple concurrent clinical research studies, data collection, specimen management, database maintenance, and compliance with UCSF and regulatory agency policies for the Genitourinary Oncology program. Responsibilities
Support management and coordination of single or multiple clinical research studies. Act as intermediary among services and departments, oversee data and specimen management, and report study results. Create, clean, update, and manage databases and comprehensive datasets. Coordinate staff work schedules, assist in training of Assistant CRCs, and assist the Research Personnel Manager and/or PI with oversight of other research staff. Help assure compliance with all relevant regulatory agencies and maintain study data integrity. Implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation. Maintain relevant regulatory documents and report study progress to investigators. Participate in internal and external audits or reviews of study protocols and perform other duties as assigned. Required Qualifications
HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties. Attention to detail; strong interpersonal skills; excellent verbal and written communication; ability to multi‑task in a fast‑paced environment with a diverse subject population. Ability to work well independently, complete projects in a timely manner, and prioritize multiple projects to ensure completion of essential tasks by deadlines. Demonstrated knowledge and understanding of research, especially in the areas of biological sciences. Prior experience with computer programs (Microsoft Office, internet‑based databases) and specialized software such as OnCore. Ability to sit and work at a computer for several hours per day; may need to travel between UCSF campuses via shuttle; ability to stand for several hours of the day. Experience in clinical research or demonstrated knowledge of research training that translates into a clinical research setting; familiarity with specimen processing. Working knowledge of 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. Preferred Qualifications
Prior analytical and writing skills in a science/research environment. Fluency in the usage of Committee of Human Research (CHR) online iMEDris system for submission, renewal, and modification of protocols through the system. Understanding of patient population to create rapport and a relationship. Experience with electronic medical records. Knowledge of UCSF and departmental policies for reimbursement, guidelines for research, confidentiality, and HIPAA regulations. Knowledge of clinical research in breast oncology and experience managing oncology clinical trials. Membership in a clinical research professional society. Experience applying Good Clinical Practice Guidelines, HIPAA, the Protection of Human Research Subjects, and CHR regulations for recruitment and consent of research subjects. Salary and Benefits
Salary range: $34.32 – $55.19 per hour. To learn more about the benefits of working at UCSF, visit:
UCSF Compensation and Benefits . Equal Employment Opportunity
The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law.
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University of California, San Francisco — Helen Diller Family Comprehensive Cancer Center Job Summary
The Clinical Research Coordinator (CRC) will independently or with general direction at the fully operational level execute, manage, and coordinate research protocols under the direction of the Lead Clinical Research Coordinator, Principal Investigator (PI), and/or the Research Personnel Manager for the Investigational Trials Unit. This includes coordination of multiple concurrent clinical research studies, data collection, specimen management, database maintenance, and compliance with UCSF and regulatory agency policies for the Genitourinary Oncology program. Responsibilities
Support management and coordination of single or multiple clinical research studies. Act as intermediary among services and departments, oversee data and specimen management, and report study results. Create, clean, update, and manage databases and comprehensive datasets. Coordinate staff work schedules, assist in training of Assistant CRCs, and assist the Research Personnel Manager and/or PI with oversight of other research staff. Help assure compliance with all relevant regulatory agencies and maintain study data integrity. Implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation. Maintain relevant regulatory documents and report study progress to investigators. Participate in internal and external audits or reviews of study protocols and perform other duties as assigned. Required Qualifications
HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties. Attention to detail; strong interpersonal skills; excellent verbal and written communication; ability to multi‑task in a fast‑paced environment with a diverse subject population. Ability to work well independently, complete projects in a timely manner, and prioritize multiple projects to ensure completion of essential tasks by deadlines. Demonstrated knowledge and understanding of research, especially in the areas of biological sciences. Prior experience with computer programs (Microsoft Office, internet‑based databases) and specialized software such as OnCore. Ability to sit and work at a computer for several hours per day; may need to travel between UCSF campuses via shuttle; ability to stand for several hours of the day. Experience in clinical research or demonstrated knowledge of research training that translates into a clinical research setting; familiarity with specimen processing. Working knowledge of 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. Preferred Qualifications
Prior analytical and writing skills in a science/research environment. Fluency in the usage of Committee of Human Research (CHR) online iMEDris system for submission, renewal, and modification of protocols through the system. Understanding of patient population to create rapport and a relationship. Experience with electronic medical records. Knowledge of UCSF and departmental policies for reimbursement, guidelines for research, confidentiality, and HIPAA regulations. Knowledge of clinical research in breast oncology and experience managing oncology clinical trials. Membership in a clinical research professional society. Experience applying Good Clinical Practice Guidelines, HIPAA, the Protection of Human Research Subjects, and CHR regulations for recruitment and consent of research subjects. Salary and Benefits
Salary range: $34.32 – $55.19 per hour. To learn more about the benefits of working at UCSF, visit:
UCSF Compensation and Benefits . Equal Employment Opportunity
The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law.
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