19 days old

Clinical Research Coordinator

Kelly Services
Garden Grove, CA 92841
**Full-Time Research Coordinator**

**Kelly Science is assisting with hiring a** Research Coordinator to be primarily responsible to function as a back-up Study Coordinator in the coordination and participation of clinical research studies conducted by principal investigators. Position is located in Garden Grove, CA.


+ Variety of complex activities involved in the collection, compilation, documentation and analysis of clinical research data under the direct supervision of the Principal Investigator.

+ Study Execution Lead patient identification efforts by active screening activities from investigator s clinics, hospital, referral networks, marketing, etc.

+ Screens potential patients for protocol eligibility.

+ Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls/randomizes patients on protocol.

+ Coordinates patient care in compliance with protocol requirements. Provides a safe environment for patients, families, and clinical staff at all time through compliance with all federal, state, and professional regulatory standards as issued through OSHA, FDA, and ICH.

+ Maintains strict patient confidentiality according to HIPAA regulations and applicable law. In collaboration with the physician, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings.

+ May disburse investigational drug and provide patient teaching regarding administration.

+ Coordinates and maintains investigational drug accountability.

+ Coordinate and implement procedures to collect data from patient charts, medical records, interviews, questionnaires, diagnostic tests and other sources; code, evaluate and interpret collected data and prepare appropriate documentation; obtain blood samples, cultures, tissues and other specimens for laboratory analysis.

+ Ensure compliance with protocol guidelines and requirements of regulatory agencies; identify problems and/or inconsistencies and monitor patients progress to include documentation and reporting of adverse events; recommend corrective action as appropriate.

+ Responsible for accurate and timely data collection, documentation, entry, and reporting.

+ Schedules and participates in monitoring and auditing activities.


+ BS degree in Life Science or Public Health with a preference in Psychology.

+ Demonstrated experience with patient consent processes

+ Phase I-II clinical trial experience is preferred.

**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. (
Posted: 2021-04-19 Expires: 2021-05-20

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Clinical Research Coordinator

Kelly Services
Garden Grove, CA 92841

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