Clinical Research Associate - Oncology - Los Angeles, CA (Field Based)

PRA International; Los Angeles (CA); On-site; USD 91,000 - 115,000; Full time

Job summary

A leading clinical research organization seeks a Clinical Research Associate in Los Angeles, responsible for managing oncology trials and mentoring staff. The ideal candidate will have significant experience in clinical monitoring, particularly in oncology, along with strong communication skills and knowledge of regulatory guidelines. This role offers a competitive salary and a range of benefits in an inclusive environment.

Benefits

Competitive salary

Health insurance

Retirement plans

Employee Assistance Program

Flexible benefits

Qualifications

• 2-3 years' experience in clinical trial monitoring.
• 1-3 years' experience in Oncology trial monitoring.
• Knowledge of GCP, ICH guidelines, and local regulations.

Responsibilities

• Managing multiple oncology trials and mentoring junior team members.
• Reviewing study documents and supporting budget development.
• Monitoring metrics and KPIs as per the Quality Oversight Plan.

Skills

Patient recruitment strategies

Collaboration

Leadership

Communication

Risk-based monitoring

Education

B.S. or R.N. in Biological Sciences

Tools

CTMS

EDC

eTMF

IWRS

Safety reporting systems

Job description

Overview

As a Clinical Research Associate, you will join the world’s largest and most comprehensive clinical research organization, powered by healthcare intelligence.

Responsibilities

What will you be doing?

• Managing multiple trials within Oncology
• Focusing on quality of life with regional travel
• Demonstrating leadership through involvement in initiatives and serving as SME for systems and processes
• Mentoring and coaching junior team members
• Training other Study Managers (SMs) and acting as Lead SM
• Developing site start-up documents, including SIV agenda
• Reviewing study documents as SM voice (e.g., Monitoring Guidelines)
• Representing Lead Trial Managers (LTMs) or SMs in meetings
• Reviewing reports for sites assigned to other SMs within the same trial
• Supporting country budget development and contract negotiations in collaboration with CCS colleagues
• Assisting with ASV processes
• Monitoring metrics and KPIs as outlined in the Quality Oversight Plan (QOP)

Interfaces – Primary and Others:

• Primary: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager, Central Study Team
• Others: Study Responsible Physician, Regional Quality and Compliance Manager, Local Drug Safety Officer, Site Manager team, Investigators, and site personnel

Qualifications

You Are:

• B.S., R.N., or equivalent in Biological Sciences
• Located near a major airport in Los Angeles, California
• With 2-3 years’ experience in clinical trial monitoring
• With 1-3 years' experience in Oncology trial monitoring
• Knowledge of therapeutic areas and risk-based monitoring
• Skilled in patient recruitment strategies and partner collaboration
• Proficient with CTMS, EDC, eTMF, dashboards, IWRS, safety reporting systems
• Strong communicator with the ability to work independently and as part of a team
• In-depth knowledge of GCP, ICH guidelines, and local regulations
• Willing to travel up to 50%
• Legally authorized to work in the US without future sponsorship

Pay Range: $91,336 - $114,170 USD

Salary depends on location, experience, education, and skills.

What ICON offers: Competitive salary, diverse culture, benefits including leave, health insurance, retirement plans, Employee Assistance Program, life insurance, and flexible benefits. Learn more at ICON Careers Benefits. ICON values inclusion and accessibility, providing accommodations for applicants with disabilities. We encourage you to apply even if you do not meet all requirements.