University of California - San Francisco
Clinical Research Coordinator - Dermatology
University of California - San Francisco, San Francisco, California, United States, 94199
Clinical Research Coordinator - Dermatology
DermatologyFull Time81007BRJob SummaryThe UCSF Department of Dermatology is committed to advancing healthcare through cutting-edge clinical research. We are currently seeking an experienced Clinical Research Coordinator (CRC) with a strong background in conducting industry-sponsored clinical trials to join our dedicated team.As a CRC, you will play a crucial role in the planning, coordination, and execution of multiple industry-sponsored clinical trials. The successful candidate will bring expertise in managing all aspects of research studies, ensuring compliance with regulatory requirements, and fostering positive relationships with sponsors and research participants.The duties may include, but will not be limited to:Study Coordination
Oversee the day-to-day operations of assigned clinical trials, ensuring adherence to protocols, timelines, and quality standards.Collaborate with principal investigators, study sponsors, and cross-functional teams to facilitate smooth study implementation.
Regulatory Compliance
Ensure compliance with regulatory requirements, including FDA guidelines and Good Clinical Practice (GCP) standards.Prepare and submit regulatory documents for Institutional Review Board (IRB) approval and maintain ongoing regulatory documentation.
Participant Recruitment and Retention
Develop and implement effective strategies for participant recruitment and retention.Coordinate study visits, including scheduling, monitoring, and ensuring participant safety and satisfaction.
Data Management
Oversee data collection, entry, and quality control procedures.Work closely with data management teams to ensure accurate and timely data submission to sponsors and regulatory authorities.
Communication
Serve as the primary point of contact for sponsors, investigators, and research staff.
Communicate study progress, issues, and resolutions effectively to internal and external stakeholders.The final salary and offer components are subject to additional approvals based on UC policy. Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. The salary range for this position is $34.32 - $55.19 (Hourly Rate).To learn more about the benefits of working at UCSF, including total compensation, please visit:
UCSF BenefitsDepartment DescriptionUCSF Dermatology is a global leader providing outstanding care for patients with skin disease, training the next generation, advancing innovative research, and advocating for the health of our communities. We rank among the world's top centers for skin research.Required QualificationsHS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities;
and/or equivalent experience/training .Strong knowledge of regulatory requirements, GCP, and FDA guidelines.Proficiency in electronic data capture systems and Microsoft Office Suite.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 QualificationsCertification in clinical research (e.g., SoCRA or ACRP) is a plus.Two (2) years of experience as a Clinical Research Coordinator with a focus on industry-sponsored trials.Fluency in the usage of Committee of Human Research (CHR) online iMEDris system for submission, renewal, and modification of protocols.Understanding of patient population to create rapport and a relationship, while also giving insight to what is realistic and appropriate for patient participation.Experience with electronic medical records.About UCSFThe University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care.Pride ValuesUCSF is a diverse community made of people with many skills and talents. We seek candidates whose work experience or community service has prepared them to contribute to our commitment to professionalism, respect, integrity, diversity, and excellence - also known as our PRIDE values.Equal Employment OpportunityThe University of California San Francisco is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information.OrganizationCampusJob Code and Payroll Title009335 CLIN RSCH CRDJob CategoryResearch and ScientificBargaining UnitUniversity Professional Technical Employees - Research Support Professionals Unit (UPTE-RX)Employee ClassCareerPercentage100%LocationMount Zion (SF)ShiftDaysShift Length8 HoursAdditional Shift DetailsMonday - Friday
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DermatologyFull Time81007BRJob SummaryThe UCSF Department of Dermatology is committed to advancing healthcare through cutting-edge clinical research. We are currently seeking an experienced Clinical Research Coordinator (CRC) with a strong background in conducting industry-sponsored clinical trials to join our dedicated team.As a CRC, you will play a crucial role in the planning, coordination, and execution of multiple industry-sponsored clinical trials. The successful candidate will bring expertise in managing all aspects of research studies, ensuring compliance with regulatory requirements, and fostering positive relationships with sponsors and research participants.The duties may include, but will not be limited to:Study Coordination
Oversee the day-to-day operations of assigned clinical trials, ensuring adherence to protocols, timelines, and quality standards.Collaborate with principal investigators, study sponsors, and cross-functional teams to facilitate smooth study implementation.
Regulatory Compliance
Ensure compliance with regulatory requirements, including FDA guidelines and Good Clinical Practice (GCP) standards.Prepare and submit regulatory documents for Institutional Review Board (IRB) approval and maintain ongoing regulatory documentation.
Participant Recruitment and Retention
Develop and implement effective strategies for participant recruitment and retention.Coordinate study visits, including scheduling, monitoring, and ensuring participant safety and satisfaction.
Data Management
Oversee data collection, entry, and quality control procedures.Work closely with data management teams to ensure accurate and timely data submission to sponsors and regulatory authorities.
Communication
Serve as the primary point of contact for sponsors, investigators, and research staff.
Communicate study progress, issues, and resolutions effectively to internal and external stakeholders.The final salary and offer components are subject to additional approvals based on UC policy. Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. The salary range for this position is $34.32 - $55.19 (Hourly Rate).To learn more about the benefits of working at UCSF, including total compensation, please visit:
UCSF BenefitsDepartment DescriptionUCSF Dermatology is a global leader providing outstanding care for patients with skin disease, training the next generation, advancing innovative research, and advocating for the health of our communities. We rank among the world's top centers for skin research.Required QualificationsHS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities;
and/or equivalent experience/training .Strong knowledge of regulatory requirements, GCP, and FDA guidelines.Proficiency in electronic data capture systems and Microsoft Office Suite.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 QualificationsCertification in clinical research (e.g., SoCRA or ACRP) is a plus.Two (2) years of experience as a Clinical Research Coordinator with a focus on industry-sponsored trials.Fluency in the usage of Committee of Human Research (CHR) online iMEDris system for submission, renewal, and modification of protocols.Understanding of patient population to create rapport and a relationship, while also giving insight to what is realistic and appropriate for patient participation.Experience with electronic medical records.About UCSFThe University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care.Pride ValuesUCSF is a diverse community made of people with many skills and talents. We seek candidates whose work experience or community service has prepared them to contribute to our commitment to professionalism, respect, integrity, diversity, and excellence - also known as our PRIDE values.Equal Employment OpportunityThe University of California San Francisco is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information.OrganizationCampusJob Code and Payroll Title009335 CLIN RSCH CRDJob CategoryResearch and ScientificBargaining UnitUniversity Professional Technical Employees - Research Support Professionals Unit (UPTE-RX)Employee ClassCareerPercentage100%LocationMount Zion (SF)ShiftDaysShift Length8 HoursAdditional Shift DetailsMonday - Friday
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