Clinical Research Coordinator

University of California, San Francisco; Oakland (CA); On-site; USD 60,000 - 80,000; Full time

Job summary

The University of California, San Francisco is seeking a Clinical Research Coordinator to manage and coordinate various research protocols, contributing to impactful studies in public health. The role requires excellent communication skills, the ability to work independently, and a strong attention to detail while supporting HIV-related research initiatives.

Qualifications

• Experience in public health, epidemiology, or related fields preferred.
• Minimum of 2 years related research experience.
• HS graduation with equivalent training also acceptable.

Responsibilities

• Coordinate and manage multiple clinical research studies.
• Recruit and screen new enrollees for studies.
• Oversee data collection and maintain compliance with regulatory agencies.

Skills

Attention to detail

Interpersonal skills

Verbal communication

Written communication

Multi-tasking

Education

High School graduation

Job description

Join to apply for the Clinical Research Coordinator role at University of California, San Francisco

Join to apply for the Clinical Research Coordinator role at University of California, San Francisco

Job Summary

The Clinical Research Coordinator will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Clinical Research Supervisor, Associate Project Director, and/or Principal Investigator (PI); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.

MED-VAMC-INFD

Full Time

85117BR

Job Summary

The Clinical Research Coordinator will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Clinical Research Supervisor, Associate Project Director, and/or Principal Investigator (PI); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.

The Clinical Research Coordinator will independently execute, manage, and coordinate multiple clinical research protocols within the MACS/WIHS Combined Cohort Study (MWCCS) - a collaborative, multi-center, longitudinal study designed to comprehensively investigate the impact of chronic health conditions that affect people with HIV. CRC duties may include, but will not be limited to recruiting and screening new enrollees, supporting the management and coordinating the tasks of multiple concurrent clinical research studies; the CRC will act as the study liaison to the Community Advisory Board (CAB) and write the quarterly MWCCS Newsletter to disseminate information to study participants; act as intermediary between services and departments while overseeing data and specimen collection; clean and update, databases and comprehensive datasets and reports; coordinate staff work schedules, assist with training of new CRCs; may assist with management of Investigator’s protocols in the Investigational Review Board online system, as well as renewals and modifications of protocol applications and the implementation of new studies; help assure compliance with all relevant regulatory agencies; oversee study data integrity; implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation; maintain all regulatory documents; report study progress to investigators; participate in any internal and external audits or reviews of study protocols; and perform other duties as assigned.

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. For positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement.

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: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html

Department Description

The Department of Medicine (DOM), the largest department in the School of Medicine, has close to 600 full- time faculty leading top-notch research, clinical, and education programs. The Department has a decentralized organizational structure across four sites (Parnassus, ZSFG, SFVAHCS and Mt. Zion) and 38 divisions. Authority and accountability for the Department rests with the Department Chair who heads the Parnassus and Mt. Zion sites, and also directs the Vice Chairs at the ZSFG and SFVAHCS sites.

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

• BA/BS and a minimum of 2 years of related research or work experience in public health, epidemiology, health promotion, social sciences, or related field or an equivalent combination of education and experience.
• Certified Phlebotomist (CPT-1)
• Demonstrated history of excellent attendance, reliability, and dependability.
• Previous experience in HIV-related clinical research and the ability to adhere to structured protocols.
• Fluency in the usage of Investigational Review Board (IRB) online iRIS system for submission, renewal, and modification of protocols through this system.
• Understanding of patient population (e.g. HIV, drug users, mental health challenges) 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.
• 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: SalesForce,
• 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
  

About UCSF

The 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. It is the only campus in the 10-campus UC system dedicated exclusively to the health sciences. We bring together the world’s leading experts in nearly every area of health. We are home to five Nobel laureates who have advanced the understanding of cancer, neurodegenerative diseases, aging and stem cells.

Pride Values

UCSF 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.

In addition to our PRIDE values, UCSF is committed to equity – both in how we deliver care as well as our workforce. We are committed to building a broadly diverse community, nurturing a culture that is welcoming and supportive, and engaging diverse ideas for the provision of culturally competent education, discovery, and patient care. Additional information about UCSF is available at diversity.ucsf.edu

Join us to find a rewarding career contributing to improving healthcare worldwide.

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.

Organization

Campus

Job Code and Payroll Title

009335 CLIN RSCH CRD

Job Category

Research and Scientific

Bargaining Unit

University Professional Technical Employees – Research Support Professionals Unit (UPTE-RX)

Employee Class

Career

Percentage

100%

Location

Oakland, CA

Work Style

Fully On-Site

Shift

Days

Shift Length

8 Hours

Additional Shift Details

Monday - Friday, 8:30am - 5:00pm

Seniority level

• Seniority level

  Not Applicable

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Higher Education

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