Top 20 Research specialist Jobs in Uci Ca

Specialist, Clinical Research Monitoring
Edwards Lifesciences —Irvine, CA
- $87,000 - $123,000 a year
- Full-time
- Analysis skills
- Bachelor's degree
- Continuous improvement
2d
Clinical Research Specialist
BiVACOR Inc —Huntington Beach, CA
- $90,000 - $118,000 a year
- Full-time
- Mid-level
- Bachelor's degree
- Travel
- Health savings account
- Health insurance
Quick Apply
Principal Clinical Research Analyst - Class III Medical Devices (EU MDR Clinical Affairs Expert)
BIOTRONIK —Tustin, CA
- $165,000 - $185,000 a year
- Online Application
- Hybrid work
- 7 years
- Office
- Bachelor's degree
- Health savings account
- Health insurance
8d
Sr. Program Lead, Professional Education, CKMH
American Heart Association —Irvine, CA
- $84,400 - $113,000 a year
- Full-time
- Remote
- 5 years
- Bachelor's degree
- Fair chance
- Wellness program
- Paid holidays
Payment Poster & Research Specialists
HUCKEYE HEALTH SERVICES LLC —Costa Mesa, CA
- $20 - $25 an hour
- Online Application
- Mid-level
- High school diploma or GED
- 2 years
Quick Apply
Donor Prospect Research Specialist (Advancement Professional I)
California State University —Fullerton, CA
- Online Application
- Background check
- Research
- Mid-level
- Paid holidays
- Health insurance
Specialist, Clinical Safety (US Remote)
MicroVention, Inc. —Aliso Viejo, CA
- $105,067 - $131,333 a year
- Remote
- Medicine
- Microsoft Outlook
- Mid-level
Specialist, Clinical Compliance
JENAVALVE TECHNOLOGY INC —Irvine, CA
- $80,000 - $90,000 a year
- Full-time
- Microsoft Excel
- Mid-level
- Bachelor's degree
Quick Apply
Specialist, Clinical Safety
JENAVALVE TECHNOLOGY INC —Irvine, CA
- $100,000 a year
- Full-time
- Medicine
- Microsoft Excel
- Microsoft Outlook
Quick Apply
R&D - Regulatory Compliance Specialist II
Pulmuone Foods USA, Inc. —Fullerton, CA
- $80,000 - $90,000 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- English
- Disability insurance
- Health insurance
Quick Apply
Clinical Laboratory Scientist Specialist-Fulltime-Laboratory-Lakewood-Variable
University of California, Irvine —Lakewood, CA
- $62.36 - $90.82 an hour
- Full-time
- Background check
- Customer service
- Bachelor of Science
- Health insurance
- Retirement plan
11h
Principal Clinical Research Analyst - Class III Medical Devices (EU MDR Clinical Affairs Expert)
BIOTRONIK SE & Co. KG —Tustin, CA
- $165,000 - $185,000 a year
- Online Application
- Hybrid work
- 7 years
- Office
- Bachelor's degree
- Health insurance
- Paid time off
10d
Senior Tax Research Specialist
CSC (Corporation Service Company) —United States
- Full-time
- Remote
- Computer science
- Azure
- CPA

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Senior Research Analyst
Confidential —Irvine, CA
Serve as a trusted resource by researching and obtaining answers to property-specific questions through direct communication and independent research.
$30 - $35 an hour
Quick Apply
14d
Principal Clinical Research Analyst - Class III Medical Devices (EU MDR Clinical Affairs Expert)
BIOTRONIK —Tustin, CA
We are seeking a highly experienced *Principal Clinical Research Analyst - Class III Medical Devices (EU MDR Clinical Affairs Expert)* to provide strategic…
$165,000 - $185,000 a year
8d

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Specialist, Clinical Research Monitoring

Edwards Lifesciences -
Irvine, CA

Apply Now

Job Details

Full-time
$87,000 - $123,000 a year
2 days ago

Qualifications

Research regulatory compliance
Clinical quality assurance standards

Full Job Description

Imagine how your ideas and expertise can change a patient’s life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how our products transform patients’ lives. As part of our Clinical Affairs team, you’ll hone your scientific curiosity and passion for evaluating data to increase access to pioneering technologies for patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize patient outcomes.

Innovation starts from the heart. Our Advanced Innovation & Technology (AI&T) teams harness the imagination, courage, and resourcefulness to think beyond what’s currently possible, and create solutions for patients many years into the future. If you’re an early-stage innovator, then Edwards AI&T team is the place for you to take the next steps in your career. We’ll give you the tools and resources you need to create groundbreaking innovations that shape the future of structural heart technology.

This position requires travel through the West Coast region. Highly prefer candidates based on the West Coast (CA, OR, AZ, NV, WA). Selected candidate must reside in local region.

How you will make an impact:

Field monitoring of studies and data collection for clinical trials, assessing all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determining if clinical trial/study subject documentation is within parameters of study hypothesis, as well as monitoring clinical trial/study safety, in keeping with protocols, GCP (Good Clinical Practices) and regulatory requirements.
Providing oversight of and insights into trial activities (e.g., trends in protocol compliance, enrollment, monitoring deviations, data quality) to principal investigators and support staff, and study sponsor management and leadership staff, including Institutional Review Boards/Ethics Committees/Research Ethics Committees, Clinical Operations (e.g. Contracts), and recommending and developing process improvements.
Verifying trial/study data, including maintaining appropriate regulatory documents both internal and external, auditing to be sure the site has the appropriate regulatory documentation to conduct the trial/study, and source documentation is properly recorded.
Validating investigational device accountability by tracking the history of investigational devices from Edwards to the field sites and through final disposition.
Developing and delivering training on GCPs, protocols, database, compliance, device accountability, adverse event reporting, study investigation protocols, amendments, regulatory documentation requirements as well as training and proctoring new employees on trial and study related activities.
Contributing to the development of clinical protocols, informed consent forms, and case report forms.
Editing/amending informed consent documents.

What you’ll need (Required):

Bachelor's Degree or equivalent in related field with 3 years of field monitoring, quality assurance/control and regulatory compliance experience or equivalent work experience based on Edwards criteria.

What else we look for (Preferred):

Clinical research certification (ACRP or SoCRA clinical coordinator/CRA certification)
Strong written and verbal communication skills, presentation skills, interpersonal skills, and analytical skills
Proven expertise in MS Office Suite, including Word, Excel, Adobe, and ability to operate general computer software and office machinery
Demonstrated problem-solving and critical thinking skills
Strong understanding of cardiovascular anatomy, pathology and physiology or Business Unit area of expertise
Substantial understanding of medical device regulatory requirements and documents, device accountability and adverse events reporting
Technical writing skills (protocols, CRF development, study tools)
Ability to communicate and relate well with key opinion leaders and clinical personnel

Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.

For California (CA), the base pay range for this position is $87,000 to $123,000 (highly experienced).

The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.

Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.

Apply Now

Refine Your Search

research specialist jobs in uci ca

Specialist, Clinical Research Monitoring

Clinical Research Specialist

Principal Clinical Research Analyst - Class III Medical Devices (EU MDR Clinical Affairs Expert)

Sr. Program Lead, Professional Education, CKMH

Payment Poster & Research Specialists

Donor Prospect Research Specialist (Advancement Professional I)

Specialist, Clinical Safety (US Remote)

Specialist, Clinical Compliance

Specialist, Clinical Safety

R&D - Regulatory Compliance Specialist II

Clinical Laboratory Scientist Specialist-Fulltime-Laboratory-Lakewood-Variable

Principal Clinical Research Analyst - Class III Medical Devices (EU MDR Clinical Affairs Expert)

Senior Tax Research Specialist

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