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 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.
Incumbent’s duties may include, but will not be limited to supporting the management and coordinating the tasks of multiple clinical research studies, depending on their size and complexity; act as intermediary between services and departments while overseeing data and specimen management; manage and report on study results; create, clean, update, and manage databases and comprehensive datasets and reports; coordinate staff work schedules, assist with training of Assistant CRCs, and assist Clinical Research Supervisor and/or PI with oversight of other research staff; manage Investigator’s protocols in the Committee on Human Research online system, as well as renewals and modifications of protocol applications and the implementation of new studies; participate in the review and writing of protocols to ensure institutional review board approval within University compliance; 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 Lupo Lab in the Department of Radiology and Biomedical Imaging is a research center focused on the development, implementation and application of novel imaging techniques to patients with the goal of improving
the characterization and assessment of response to therapy in patients with brain tumors and other neurological diseases. Researchers working in the Lupo Lab work closely with clinicians in the Neuro-Oncology Service and scientists at the Brain Tumor Research Center in order to evaluate the new techniques that are developed. The populations of patients that are considered are individuals who are being scanned prior to surgical resection or are participating in serial studies of response to therapy. Support comes from industry contracts, investigator initiated studies that are performed in collaboration with other academic institutions, or from NIH supported programmatic and individual investigator research grants.
The Clinical Research Coordinator (CRC) will work under the supervision of Dr. Janine Lupo and will play a critical role in managing all aspects of brain tumor imaging patient studies. This requires a close interaction with staff in the Neuro-Oncology service in order to recruit and schedule patient scans, collect clinical data, and keep track of recruitment to specific research studies. The CRC will support brain tumor imaging studies in the Lupo and Li Labs with regard to project management, compliance with the regulatory and UCSF policies, interacting with patients, and collecting data to meet the reporting requirements of industry and other granting agencies. The latter of which can include data acquisition on the scanners, data post-processing, entry, as well as planning and recording the locations of image-guided tissue samples during surgery according to guidelines defined by research grants

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

• Two years of experience in administrative analysis or clinical research
• Prior experience with: developing and coordinating clinical research studies and managing multiple protocols, data abstraction and entry; project management.
• Familiarity with MS Office: Word, Excel, PowerPoint
• 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 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: 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

Please refer the Job description for details