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13 days old

Clinical Research Coordinator

Kelly Services
Sacramento, CA 94278
Kelly is hiring a **Clinical Research Coordinator** for one of our clients in **Sacramento, CA**


+ Pay: Negotiable

+ **Location:** Mercy Cancer Center, 3301 C Street, Suite 550, Sacramento, CA 95816

+ 1 year assignment


**Traveler will also FLOAT to the following locations as needed:**


+ Mercy Cancer Center, 6511 Coyle Avenue, Suite 200, Carmichael, CA 95608

+ Mercy Cancer Center, 550 W Ranch View Drive, Suite 3000, Rocklin, CA 95765

+ Mercy Cancer Center, 9394 Big Horn Blvd, Elk Grove, CA 95758

+ Woodland Cancer Center, 515 Fairchild Court, Woodland, CA 95695


**The Senior Clinical Research Coordinator (SCRC)** works with the Dignity Health Research Institute Market Clinical Research Manager (MCRM), Principal Investigators, co- and sub- investigators, clinical and ancillary departments, IRBs, and industry or government sponsors of research to plan, coordinate, implement and complete clinical trials and other research projects managed by the Dignity Health Research Institute. The incumbent has responsibility for the oversight of studies that explore complex medical diseases, which involve specialty and subspecialty expertise. The incumbent independently manages all aspects of multiple clinical trials or other research projects as assigned, including but not limited to: research participant recruitment, screening and enrollment; completion of protocol required visits and procedures; collection and reporting of data; coordination of and participation in sponsor monitoring visits or federal audits; query resolution; adverse event reporting, source documentation and research record development and maintenance; study drug accountability; specimen collection, processing and shipment. The incumbent works with the MCRM to ensure compliance of the research program and its studies with all applicable federal and state regulations, as well as Dignity Health policy


In addition to managing clinical trials, the Senior Clinical Research Coordinator will provide training and mentorship, project leadership, and quality control oversight of Clinical Research Associate and Clinical Research Coordinator positions. This position is responsible for maintaining quality standards for responsive service and professional documentation in compliance with Dignity Health policies and procedures, and federal and state laws and regulations, all which is consistent with the Mission and Values of Dignity Health. This is an exempt position that may require occasional overnight travel and weekend assignments.


**SUBMISSION REQUIREMENTS**


+ **1 Year Assignment Commitment (to start) - REQUIRED**

+ **7 years** or more Research experience - Required

+ Must be willing to Float - Required

+ Bachelor Degree (or higher) - RequiredCurrent certification (CCRP or CCRC) by the Society of Clinical Research Associates (SOCRA) or Association of Clinical Research Professionals (ACRP) required.Current certificate of Human Subjects Protection and Good Clinical Practice training required.

+ Minimum 7 years of experience conducting clinical trials required; worked as primary research coordinator for at least 20 drug or device trials.

+ Minimum 7 years of experience interacting with patients in a healthcare setting required.

+ Thorough knowledge and understanding of research regulatory requirements involving human subjects research, including FDA, OHRP and GCP requirements required.

+ Experience in implementation of research protocols and clinical trials processes required

+ Experience in preparing and maintaining regulatory documents and other IRB-related study documentation required.

+ Experience training staff and/or investigators on clinical trial processes and improvement techniques preferred.

+ Experience using electronic data capture software required; Clinical Trial Management Systems (CTMS) preferred.

+ Experience with Microsoft Office software required.

+ Knowledge of medical terminology required.

+ Lab processing experience required.

+ Phlebotomy certification preferred.

+ IDX EMR experience - Preferred

+ BLS and First Aid Certification Preferred

+ IATA and/or Safe-T-Pak Certification for shipment of lab specimens and/or dry ice - Preferred


**CERTIFICATION REQUIREMENTS**


+ BLS (AHA)


**Why Kelly** **** **?**


Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire talented people just like you. Every day, we match science professionals with dream jobs that fit their skills and interestsits the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background/education in science, so we know a thing or two about the science market and how to get you noticed.


**About Kelly** ****


At Kelly, were always thinking about whats next and advising job seekers on new ways of working to reach their full potential. In fact, were a leading advocate for temporary/nontraditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live (plus, did we mention we provide a ton of benefits ?). Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world.


Kelly is an equal opportunity employer committed to employing a diverse workforce, including, but not limited to, minorities, females, individuals with disabilities, protected veterans, sexual orientation, gender identity. Equal Employment Opportunity is The Law. (https://www.dol.gov/ofccp/regs/compliance/posters/ofccpost.htm)

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Posted: 2021-10-04 Expires: 2021-11-04

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Clinical Research Coordinator

Kelly Services
Sacramento, CA 94278

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