Clinical Operations Specialist job in Irvine, CA
Vacancy has expired
Irvine, CA CorTech LLC
| Job Ref: | 372839 |
| Employer: |
CorTech LLC |
| Job Type: | Contract |
| Salary and Benefits: | 43.00/Per Hour |
| Remote: | No |
Location |
|
| City: | Irvine, CA |
| Post Code: | 92618 |
| Map: |
|
Description |
|
|
JobsRUs.com is seeking to hire a Clinical Operations Specialist for our client in Irvine, CA! Benefits Available Weekly Pay! Pay Rate - $38-48/hr 1st Shift: Monday-Friday, 8am-5pm Job Description This role is focused on study device management and you'll be supporting onsite research activities. Identify, develop, recommend, and implement, moderately complex process development and process improvement solutions to optimize global trial workflow timelines, (e.g., device return aging issues, status of open device issues/queries, etc.) Develop and execute device processes associated with clinical trials. Ensure compliance with regulations and manage the lifecycle of devices, while closely partnering with other internal key stakeholders ( e.g., clinical study teams, Manufacturing Operations, Finance, Supply Chain, Quality, and Compliance groups) to develop and lead the execution of the device process, and ensuring continuous process improvement of efficiency and accuracy of processes and procedures. Verify inventory and process device shipment to clinical sites within our shipping timeframe to Customer Service, Trade Compliance, and other relevant stakeholders. Confirm receipt of product with the clinical site and obtain copies of signed and dated packing slips. Monitor device inventory by coordinating with Supply Chain and Clinical Specialists Develop timeline assessments (e.g., transition to new device system, system enhancements to meet supply and demand, etc) in collaboration with clinical stakeholders in order to meet key study milestones and deadlines. Ensure documentation are archived appropriately within record retention facility (e.g., Iron Mountain, clinicaltrial.gov) 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, enter into computerized tracking system, and file/scan for archive, for multiple clinical research trials Maintains current and active licensure and certification(s) to administer First Aid, BLS and CPR for emergent needs in healthy volunteer clinical research studies Support clinical research laboratory operations as needed Other incidental duties as assigned Required: >1?2 years of patient-facing experience in a clinical research, healthcare, or related medical setting. Must have experience in a healthcare clinical environment. 2 years of allied health care experience, licensed EMT is acceptable. Current CPR and First Aid certification from an accredited provider Preferred experience/qualifications: Associate's/Bachelor?s degree in a related field Medical assistant certification is a plus BD04123JD | |
ref: (372839)
52 days ago
Back to search results