Only the job description changed.
| Previous Job Description | Current Job Description | ||||
|---|---|---|---|---|---|
| n | 1 | Job Description: | n | 1 | Job Summary |
| 2 | Job Summary Under the supervision of a Clinical Research Supervisor or Principal Investigator (PI), | ||||
| > | the incumbent will perform entry-level duties related to the support and coordination of clinical st | ||||
| > | udies, and may receive training and development to prepare and advance for journey-level work at the | ||||
| > | next level within the series. May be responsible for the coordination of one or more single or mult | ||||
| > | i-site, active or follow-up clinical trials; help prepare protocols for study initiation; help desig | ||||
| > | n flow sheets, data forms and source documents; gather and interpret medical, surgical and laborator | ||||
| > | y data regarding clinical trial subjects; may apply understanding of inclusion/exclusion eligibility | ||||
| > | criteria for protocols; help recruit, enroll, register, schedule and retain study subjects; record | ||||
| > | protocol specific treatments and assure collection and shipment of samples; assist research personne | ||||
| > | l to keep patients on study schedules; complete study forms to submit to sponsors and/or appropriate | ||||
| > | agencies; collect, enter and clean data into study databases, maintaining data quality; assist with | ||||
| > | data analysis; assist with preparation of reports and tables; attend team meetings; and perform oth | ||||
| > | er duties as assigned. Department Overview: This position is to support a study in its day-to-day op | ||||
| > | erations at Benioff Children’s Hospital. It is a limited 20% position with variable study activities | ||||
| > | at time there are times when you will be needed to work in person at the hospital from approximatel | ||||
| > | y 5pm-9pm when participants are in the pediatric cardiac ICU. Other times there are flexible hours t | ||||
| > | hat can be completed remotely. After orientation, you will be expected to work independently with co | ||||
| > | nsultation from the principal investigators. | ||||
| 3 | 2 | ||||
| t | 4 | Qualifications: | t | 3 | Under the supervision of a Clinical Research Supervisor or Principal Investigator (PI), the incumbe |
| > | nt will perform entry-level duties related to the support and coordination of clinical studies, and | ||||
| > | may receive training and development to prepare and advance for journey-level work at the next level | ||||
| > | within the series. | ||||
| 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 and sufficient experience and | ||||
| > | demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equival | ||||
| > | ent experience/training. - Excellent verbal and written communications and presentation skills; exce | ||||
| > | llent organizational skills; and excellent interpersonal skills to work effectively in a diverse tea | ||||
| > | m. - Attention to details; - Proficiency with Microsoft Word, PowerPoint, and Windows. - Excellent a | ||||
| > | nalytical and problem-solving skills. - Ability to work effectively in a fast-paced, team-based envi | ||||
| > | ronment; project management and coordination skills; ability to prioritize tasks and meet multiple d | ||||
| > | eadlines on concurrent projects. - Ability to establish cooperative working relationships with patie | ||||
| > | nts, co-workers, & physicians. Preferred Qualifications: Qualifications that an ideal candidate woul | ||||
| > | d possess, but are not minimally required for a candidate to be considered for the position. - Demon | ||||
| > | strated proficiency with medical terminology. - Experience working with patients or study subjects. | ||||
| > | - Ability to abstract data from medical records and transfer it to data collection forms or directly | ||||
| > | into databases. | ||||
| 5 | May be responsible for the coordination of one or more single or multi-site, active or follow-up cl | ||||
| > | inical trials; help prepare protocols for study initiation; help design flow sheets, data forms and | ||||
| > | source documents; gather and interpret medical, surgical and laboratory data regarding clinical tria | ||||
| > | l subjects; may apply understanding of inclusion/exclusion eligibility criteria for protocols; help | ||||
| > | recruit, enroll, register, schedule and retain study subjects; record protocol specific treatments a | ||||
| > | nd assure collection and shipment of samples; assist research personnel to keep patients on study sc | ||||
| > | hedules; complete study forms to submit to sponsors and/or appropriate agencies; collect, enter and | ||||
| > | clean data into study databases, maintaining data quality; assist with data analysis; assist with pr | ||||
| > | eparation of reports and tables; attend team meetings; and perform other duties as assigned. | ||||
| 6 | |||||
| 7 | Department Overview: | ||||
| 8 | |||||
| 9 | This position is to support a study in its day-to-day operations at Benioff Children’s Hospital. It | ||||
| > | is a limited 20% position with variable study activities at time there are times when you will be n | ||||
| > | eeded to work in person at the hospital from approximately 5pm-9pm when participants are in the pedi | ||||
| > | atric cardiac ICU. Other times there are flexible hours that can be completed remotely. After orient | ||||
| > | ation, you will be expected to work independently with consultation from the principal investigators | ||||
| > | . | ||||