University of California, San Francisco
Clinical Research Coordinator Sudden Cardiac Death Study
University of California, San Francisco, San Francisco, California, United States, 94199
Job Summary
The Clinical Research Coordinator (CRC) will execute, manage, and coordinate routine duties of the Postmortem Investigation of Sudden Cardiac Death (POST SCD) research program alongside a team of CRCs under the guidance of the Principal Investigator (PI) and/or study team. The CRC will support the management and coordination of multiple clinical research studies, act as an intermediary between the research team and collaborators, oversee data and specimen management, manage and report study results, create, clean, update, and manage databases, manage investigator’s protocols in the Committee on Human Research online system, ensure Institutional Review Board approval, maintain regulatory documents, and participate in audits.
Responsibilities
Support the management and coordination of multiple clinical research studies.
Act as intermediary between the research team and collaborators while overseeing data and specimen management.
Manage and report on study results, including creating, cleaning, updating, and managing databases.
Manage investigator’s protocols within the Committee on Human Research online system, including renewals and modifications.
Ensure compliance with all regulatory agencies and Institutional Review Board requirements.
Maintain all regulatory documents and provide study progress reports to investigators.
Participate in internal and external audits or reviews of study protocols.
Required Qualifications
High school graduation with sufficient experience or equivalent.
Attention to detail, strong verbal and written communication skills, and ability to multi-task in a fast‑paced environment.
Ability to work independently, complete projects in a timely manner, and prioritize multiple tasks.
Previous research experience or demonstrated ability to perform assigned duties.
Excellent attendance and reliability.
Interpersonal and problem‑solving skills with tact and discretion in sensitive communications.
Ability to manage multiple projects simultaneously and report detailed status updates to the research team.
Preferred Qualifications
Fluency with the Committee of Human Research (CHR) online system for protocol submission, renewal, and modification.
Familiarity with FileMaker Pro software for data collection and management.
Experience with budget management.
Experience with electronic and hard‑copy medical records.
Knowledge of UCSF research policies, regulations, and patient safety requirements.
Proficiency in database building/analysis using Access, Stata, SAS/SPSS, Teleform programming platforms.
Experience with biostatistics and epidemiological analytic techniques.
Bachelor’s degree (BA or BS) in a science or related field.
Excellent computer skills and familiarity with Microsoft Office and graphic programs.
Salary & Benefits Salary range: $37.12 - $59.69 per hour. Comprehensive benefits include health, dental, vision, and other UCSF benefits. For additional information, visit https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html.
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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Responsibilities
Support the management and coordination of multiple clinical research studies.
Act as intermediary between the research team and collaborators while overseeing data and specimen management.
Manage and report on study results, including creating, cleaning, updating, and managing databases.
Manage investigator’s protocols within the Committee on Human Research online system, including renewals and modifications.
Ensure compliance with all regulatory agencies and Institutional Review Board requirements.
Maintain all regulatory documents and provide study progress reports to investigators.
Participate in internal and external audits or reviews of study protocols.
Required Qualifications
High school graduation with sufficient experience or equivalent.
Attention to detail, strong verbal and written communication skills, and ability to multi-task in a fast‑paced environment.
Ability to work independently, complete projects in a timely manner, and prioritize multiple tasks.
Previous research experience or demonstrated ability to perform assigned duties.
Excellent attendance and reliability.
Interpersonal and problem‑solving skills with tact and discretion in sensitive communications.
Ability to manage multiple projects simultaneously and report detailed status updates to the research team.
Preferred Qualifications
Fluency with the Committee of Human Research (CHR) online system for protocol submission, renewal, and modification.
Familiarity with FileMaker Pro software for data collection and management.
Experience with budget management.
Experience with electronic and hard‑copy medical records.
Knowledge of UCSF research policies, regulations, and patient safety requirements.
Proficiency in database building/analysis using Access, Stata, SAS/SPSS, Teleform programming platforms.
Experience with biostatistics and epidemiological analytic techniques.
Bachelor’s degree (BA or BS) in a science or related field.
Excellent computer skills and familiarity with Microsoft Office and graphic programs.
Salary & Benefits Salary range: $37.12 - $59.69 per hour. Comprehensive benefits include health, dental, vision, and other UCSF benefits. For additional information, visit https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html.
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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