Top 5 Senior cra Jobs in Hawthorne Ca

Senior Clinical Research Associate
ICON Plc —Los Angeles, CA
- $110,520 - $138,150 a year
- Full-time
- Remote
- Up to 50% travel
- Bachelor's degree
- Travel
- Disability insurance
- Health insurance
Senior Clinical Research Associate
Puma Biotechnology —Los Angeles, CA
- $140,000 - $165,000 a year
- Weekends as needed
- Word processing
- 3 years
- Bachelor's degree
Sr. Clinical Research Associate
Dendreon Corporation —Seal Beach, CA
- $89,850 - $117,404 a year
- Full-time
- Microsoft Excel
- Computer literacy
- Mid-level
Sr. Clinical Research Associate
Dendreon Pharmaceuticals LLC —Seal Beach, CA
- $89,850 - $117,404 a year
- Microsoft Excel
- Computer literacy
- 3 years
2d

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Senior Clinical Research Associate
ICON Plc —Los Angeles, CA
Independently determine root causes and develop/implement site Corrective Action and Preventive Action (CAPA) plans. Life assurance and disability coverage.
$110,520 - $138,150 a year
Sr. Research Coordinator / CRC II
National Clinical Trials —Los Angeles, CA
ACRP (CCRC) or SOCRA (CCRP) certification preferred. Collaborate with principal investigators, sub-investigators, and multidisciplinary clinical teams.
$26 - $35 an hour
Quick Apply
7h

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Senior Clinical Research Associate

ICON Plc -
Los Angeles, CA

Apply Now

Job Details

Full-time
$110,520 - $138,150 a year

Benefits

Disability insurance
Health insurance
Dental insurance
Pension plan
Vision insurance
Life insurance

Qualifications

Bachelor's degree
Oncology research
Training & development
Oncology

Full Job Description

Senior Clinical Research Associate - Oncology - Los Angeles, CA

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

The Sr. Clinical Research Associate (Sr. CRA) will be responsible for performing investigative site management and monitoring activities throughout the clinical trial lifecycle. This Sr. CRA role will support the client's Oncology clinical trials to ensure data integrity, subject safety, and inspection readiness at the clinical investigative sites.

Responsibilities:

Perform site management activities to support the client's Oncology site success and maintain a continuous state of inspection readiness

Act as the primary contact and facilitate efficient communications between the the client's clinical trial team and the sites

Perform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits and Close-Out Visits) to ensure data integrity and subject safety in the client's trials

May perform oversight activities to assess monitoring quality and train/mentor less experienced CRAs

Promptly document monitoring activities and submit/approve visit reports

Manage site essential document collection and TMF reconciliation with site files

Support sites with local Institutional Review Board (IRB)/Ethics Committee (EC) submissions and confirm approvals

Regularly review site Key Risk Indicator (KRI) metrics, issues and action items to detect trends and ensure prompt resolution

Independently determine root causes and develop/implement site Corrective Action and Preventive Action (CAPA) plans

Deliver training to ensure sites comply with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs) and regulations

Support sites and the client's regulatory inspections

Contribute to site identification; drive site feasibility and qualification progress; and support site activation activities

Lead site engagement initiatives and foster relationships with key Oncology sites and networks

Qualifications

Bachelor’s degree (scientific field preferred)

5+ years monitoring clinical trials independently conducting on-site and remote monitoring visits. Atleast 2 years monitoring solid tumor clinical trials.

1+ years early development trial experience

Solid tumor clinical trial experience is required

Experience utilizing Veeva systems is highly preferred

Demonstrated experience developing/maintaining site relationships and securing compliance

Expertise in GxPs and Oncology monitoring techniques (including Risk-Based Monitoring) and terminology

Experience collaborating with sites from initial engagement through close-out phases

Experience activating sites

Experience training site staff

Experience supporting sites and/or sponsors in regulatory inspections

Experience working within a Functional Services (or in-house) monitoring model is preferred

Willing to travel up to 50%

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request .

Salary Range

$110,520.00-$138,150.00

Are you a current ICON Employee?

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