University of California – San Francisco
Research Annotator
Job Description
The Research Annotator will play a pivotal role in annotating clinical oncology notes, pathology reports, and various documents to train and evaluate large language models. Reporting to the Dr. Madhumita Sushil, who will be computer science lead and Principal Investigator (PI), and Dr. Travis Zack, who will be the clinical lead, the CRC will work closely with the PI and/or clinical lead to ensure the smooth execution of research protocols.
Responsibilities of the Clinical Research Coordinator include review and annotation of retrospective clinical documents, who are independent in problem solving and error detection, and have keen eye to details as it relates to medical information
We seek candidates with a strong background in clinical research coordination and a keen interest in leveraging their expertise to contribute to AI oncology research. The ideal candidate will possess excellent organizational and communication skills, meticulous attention to detail, and the ability to work effectively both independently and collaboratively within a multidisciplinary team environment.
The final salary and offer components are subject to additional approvals based on UC policy.
To see the salary range for this position (we recommend that you make a note of the job code and use that to look up): TCS Non-Academic Titles Search (https://tcs.ucop.edu/non-academic-titles)
Please note: An offer will take into consideration the experience of the final candidate AND the current salary level of individuals working at UCSF in a similar role.
For roles covered by a bargaining unit agreement, there will be specific rules about where a new hire would be placed on the range.
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
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
- Minimum of 2 years of experience as a Clinical Research Coordiantor with a focus on industry-sponsored trials. Experience within UCSF is a plus.
- Bachelor’s Degree in a relevant field
- Proficiency in electronic data capture systems and Microsoft Office Suite
- Certification in clinical research (e.g., SoCRA or ACRP) is a plus
- 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.
- 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
About UCSF
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
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