Spec 1, Clinical Operations

Irvine, CA - USA

Monthly Salary: Not Disclosed

Posted on: 23 hours ago

Vacancies: 1 Vacancy

Job Summary

Bill rate is $38-$48 Specialist 1 Clinical Operations

Part Time; On Site Role
8am-5pm (Tues Weds Thurs)

Job Description:

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 )
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:

At least 2 years in a clinical role such as Emergency Medical Technician or Medical Assistant
Current CPR and First Aid certification from an accredited provider
Able to work 3 days per week (Tuesday Wednesday and Thursday) with occasional flexibility to support full work weeks as needed

Preferred experience/qualifications:

Associates/Bachelors degree in a related field
>1 2 years of patient-facing experience in a clinical research healthcare or related medical setting.

Bill rate is $38-$48 Specialist 1 Clinical Operations Part Time; On Site Role8am-5pm (Tues Weds Thurs) Job Description: Identify develop recommend and implement moderately complex process development and process improvement solutions to optimize global trial workflow timelines (e.g. device ...

Bill rate is $38-$48 Specialist 1 Clinical Operations

Part Time; On Site Role
8am-5pm (Tues Weds Thurs)

Job Description:

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 )
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:

At least 2 years in a clinical role such as Emergency Medical Technician or Medical Assistant
Current CPR and First Aid certification from an accredited provider
Able to work 3 days per week (Tuesday Wednesday and Thursday) with occasional flexibility to support full work weeks as needed

Preferred experience/qualifications: