Only the job description changed.
| Previous Job Description | Current Job Description | ||||
|---|---|---|---|---|---|
| n | 1 | Job Description: | n | 1 | The Airway Clinical Research Center (ACRC) integrates research programs in asthma, COPD, sarcoidosis |
| > | , and cystic fibrosis, along with current programs sponsored by the National Institutes of Health (N | ||||
| > | IH) and the pharmaceutical industry. The Clinical Research Coordinator (CRC) will primarily be respo | ||||
| > | nsible for assisting with the coordination of NIH-sponsored studies as part of the ACE, SEARCH and P | ||||
| > | ISA Studies, as well as studies selected by the Principal Investigators (PIs) of the ACRC. | ||||
| 2 | The Airway Clinical Research Center (ACRC) integrates research programs in asthma, COPD, sarcoidosis | ||||
| > | , and cystic fibrosis, along with current programs sponsored by the National Institutes of Health (N | ||||
| > | IH) and the pharmaceutical industry. The Clinical Research Coordinator (CRC) will primarily be respo | ||||
| > | nsible for assisting with the coordination of NIH-sponsored studies as part of the ACE, SEARCH and P | ||||
| > | ISA Studies, as well as studies selected by the Principal Investigators (PIs) of the ACRC. The CRC w | ||||
| > | ill perform independently or with general direction at the fully operational journey level of the se | ||||
| > | ries to execute, manage, and coordinate research protocols, as directed by the Clinical Research Sup | ||||
| > | ervisor and / or PI; may coordinate the data collection and operations of several concurrent clinica | ||||
| > | l research studies under the guidelines of research protocols, UCSF and regulating agency policies. | ||||
| > | The CRC’s duties may include, but will not be limited to, supporting the management and coordinating | ||||
| > | the tasks of single or 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 da | ||||
| > | tasets and reports; coordinate staff work schedules, assist with training of Assistant CRCs, and ass | ||||
| > | ist Clinical Research Supervisor and / or PI with oversight of other research staff; manage Investig | ||||
| > | ator’s protocols in the Committee on Human Research (CHR) online system, as well as renewals and mod | ||||
| > | ifications 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; implem | ||||
| > | ent and maintain periodic quality control procedures; interface with departments to obtain UCSF appr | ||||
| > | oval prior to study initiation; maintain all regulatory documents; report study progress to investig | ||||
| > | ators; participate in any internal and external audits or reviews of study protocols. | ||||
| 3 | 2 | ||||
| t | 4 | Qualifications: | t | 3 | The 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 Clinical Re | ||||
| > | search Supervisor and / or PI; may coordinate the data collection and operations of several concurre | ||||
| > | nt clinical research studies under the guidelines of research protocols, UCSF and regulating agency | ||||
| > | policies. | ||||
| 5 | Required Qualifications: Qualifications that must be possessed by any candidate to be considered for | 4 | |||
| > | the position. These qualifications will be included in the job posting and will be used to screen a | ||||
| > | pplicants. Please include qualifications that are objective and quantifiable such as years of experi | ||||
| > | ence required, educational degrees, etc. Please list: - HS graduation or GED and sufficient experien | ||||
| > | ce and demonstrated skills to successfully perform the assigned duties and responsibilities - Attent | ||||
| > | ion to detail; strong interpersonal skills; excellent, effective verbal and written communication sk | ||||
| > | ills 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 p | ||||
| > | rojects to ensure the completion of essential tasks by deadlines. - Proven ability to collaborate wi | ||||
| > | th people of different professional levels - Experience working in a clinical and/or research enviro | ||||
| > | nment - Proficient in Microsoft Office Suite Required Licenses and/or Certifications: Licenses and c | ||||
| > | ertifications that a candidate must possess to be considered for the position. Please list: - N/A Pr | ||||
| > | eferred Qualifications: Qualifications that an ideal candidate would possess, but are not minimally | ||||
| > | required for a candidate to be considered for the position. Please list: - BA/BS degree with a major | ||||
| > | in science or related field and one year of experience in administrative analysis or operations res | ||||
| > | earch; or an equivalent combination of education and demonstrated skills to successfully perform the | ||||
| > | assigned duties and responsibilities - Fluency in the usage of Institutional Review Board (IRB) onl | ||||
| > | ine iRIS system for submission, renewal, and modification of protocols through this system - Underst | ||||
| > | anding 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 | ||||
| > | and administering health screening questionnaires. - Experience with internet database entry - Acti | ||||
| > | ve phlebotomy certification - Clinical trials management certification (ACRP and / or SOCRA) - Knowl | ||||
| > | edge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, conf | ||||
| > | identiality and HIPAA regulations, following the UCSF mission statement and purpose for research, an | ||||
| > | d 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 terminol | ||||
| > | ogy, research policies and guidelines, guidelines for packing/shipping infectious substances, databa | ||||
| > | se building/analysis, and data management within some of the following: Access, Stata, SASS/ SPSS, a | ||||
| > | nd Teleform programming platforms - Experience applying the following regulations and guidelines: Go | ||||
| > | od Clinical Practice Guidelines Health Information and Accountability Act (HIPAA) The Protection of | ||||
| > | Human Research Subjects IRB regulations for recruitment and consent of research subjects | ||||
| 5 | The CRC’s duties may include, but will not be limited to, supporting the management and coordinatin | ||||
| > | g the tasks of single or 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 d | ||||
| > | atasets and reports; coordinate staff work schedules, assist with training of Assistant CRCs, and as | ||||
| > | sist Clinical Research Supervisor and / or PI with oversight of other research staff; manage Investi | ||||
| > | gator’s protocols in the Committee on Human Research (CHR) online system, as well as renewals and mo | ||||
| > | difications of protocol applications and the implementation of new studies; participate in the revie | ||||
| > | w and writing of protocols to ensure institutional review board approval within University complianc | ||||
| > | e; help assure compliance with all relevant regulatory agencies; oversee study data integrity; imple | ||||
| > | ment and maintain periodic quality control procedures; interface with departments to obtain UCSF app | ||||
| > | roval prior to study initiation; maintain all regulatory documents; report study progress to investi | ||||
| > | gators; participate in any internal and external audits or reviews of study protocols. | ||||