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The Clinical Research Coordinator (CRC) 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 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 initiative this position supports is expected to take approximately two years. Required Qualifications: * HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training.
* Proficiency in data management using Excel, Access, or a similar database.
* 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:
* Bachelor's degree and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities.
* At least three months of experience in medical research.
* 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 Health Information and Accountability Act (HIPAA) 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; 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. Required Qualifications: * HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training.
* Proficiency in data management using Excel, Access, or a similar database.
* 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:
* Bachelor's degree and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities.
* At least three months of experience in medical research.
* 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 Health Information and Accountability Act (HIPAA) 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; 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. |
University of California - San Francisco
38.23 - 61.48
Apr 07, 2026