Clinical Operations Specialist Jobs in USA, CA, Irvine | Rose International Job

Rose International

Irvine, CA

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JOB DETAILS

SALARY

$35–$35 Per Hour

JOB TYPE

Temporary

SKILLS

Basic Life Support (BLS), Billing, CPR Certification, Clinical Laboratory, Clinical Research, Clinical Trial, Customer Support/Service, Document Archiving, File Maintenance, Finance, First Aid, Healthcare, Laboratory Operations, Maintain Compliance, Manufacturing Operations, Medical Products, Medicine, Process Development, Process Improvement, Product Lifecycle, Record Keeping, Regulatory Compliance, Reporting Skills, Research Laboratory, Shipping/Receiving, Supply Chain, Supply Chain Operations, Systems Administration/Management, Systems Maintenance, Time Management

LOCATION

Irvine, CA

POSTED

15 days ago

•**Only qualified Clinical Operations Specialist candidates located near the Irvine, California area to be considered due to the position requiring an onsite presence.Education: Bachelor’s degree (BA or BS) or Associate’s degree (AA or AS) in a related fieldRequired Qualifications: 1–2 years of patient facing experience in clinical research healthcare or related medical setting Current CPR and First Aid certification from an accredited providerPublic Notes: Identify develop recommend and implement moderately complex process development and process improvement solutions to optimize global trial workflow timelines Develop and execute device processes associated with clinical trials Ensure compliance with regulations and manage the lifecycle of devices while partnering with internal stakeholders including clinical study teams Manufacturing Operations Finance Supply Chain Quality and Compliance groups Verify inventory and process device shipment to clinical sites within shipping timelines while coordinating with Customer Service Trade Compliance and relevant stakeholders Confirm receipt of product with clinical sites and obtain signed and dated packing slips while monitoring device inventory with Supply Chain and Clinical Specialists Develop timeline assessments in collaboration with clinical stakeholders to meet study milestones and deadlines Ensure documentation is archived appropriately within record retention systems Track manage and coordinate clinical study invoice processing to ensure timely review approval and payment Generate reports on outstanding invoice payments for clinical study team review Review and ensure accuracy and completeness of clinical study files and maintain records in tracking systems for multiple clinical research trials Maintain current and active certification to administer First Aid BLS and CPR for clinical research studies Support clinical research laboratory operations as needed Perform other incidental duties as assigned#BD1 **Only those lawfully authorized to work in the designated country associated with the position will be considered.** **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.** Benefits: For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website. California Pay Equity: For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here. Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances. If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department. Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).

About the Company

Rose International

Founded in 1993 by Sue Bhatia, Rose International is one of the nation's leading minority- and woman-owned providers of Staffing and Total Talent Solutions. We serve companies in all 50 states and employ thousands of people across the country.

COMPANY SIZE

2,500 to 4,999 employees

INDUSTRY

Staffing/Employment Agencies

WEBSITE

https://www.roseint.com/

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