Clinical Research Associate II

ICON Strategic Solutions; Los Angeles (CA); Hybrid; USD 91,336 - 114,170; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Employee Assistance Programme

Flexible optional benefits

Job summary

ICON Strategic Solutions is looking for a Clinical Research Associate to manage and support site visits, ensuring compliance and maintaining quality data standards. The ideal candidate will have 2+ years of experience in on-site monitoring, particularly in Oncology, and will be able to communicate effectively with cross-functional teams.

The role includes benefits such as health insurance and a competitive salary ranging from $91,336 to $114,170. Residing in Los Angeles or near major hub airports for travel is preferred.

Qualifications

• 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry.
• Proficient in ICH-GCP, local regulatory requirements.
• Experienced monitoring Oncology (e.g., Prostate Cancer, Lung Cancer) and/or Hematology oncology.

Responsibilities

• Serve as the primary contact between investigational sites and the sponsor.
• Conduct site visits including selection, initiation, monitoring, and close-out.
• Ensure site compliance with regulations and maintain documentation.

Skills

On-site monitoring experience

Knowledge of ICH-GCP

Communication skills

Team collaboration

Problem-solving

Education

Bachelor's degree in Life Sciences or equivalent

Tools

CTMS

eTMF

Job description

Clinical Research Associate – Oncology – West Region

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

What You Will Be Doing

• Serve as the primary point of contact between investigational sites and the sponsor.
• Conduct all types of site visits, including selection, initiation, routine monitoring, and close‑out.
• Ensure site compliance with ICH‑GCP, SOPs, and regulations.
• Maintain up‑to‑date documentation in CTMS and eTMF systems.
• Support and track site staff training and maintain compliance records.
• Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting.
• Support subject recruitment and retention efforts at the site level.
• Oversee drug accountability and ensure proper storage, return, or destruction.
• Resolve data queries and drive timely, high‑quality data entry.
• Document site progress and elevate risks or issues to the clinical team.
• Assist in tracking site budgets and ensuring timely site payments (as applicable).
• Collaborate with cross‑functional partners including CTAs, LTMs, and CTMs.

You Are

• A graduate with a Bachelor’s degree in Life Sciences or equivalent, or a qualified RN.
• Eligible to work in the United States without visa sponsorship.
• A clinical research professional with 2+ years of on‑site monitoring experience in the pharmaceutical or CRO industry.
• Experienced monitoring Oncology (e.g., Prostate Cancer, Lung Cancer) and/or Hematology oncology.
• Proficient in ICH‑GCP, local regulatory requirements, and clinical systems such as CTMS and eTMF.
• A clear communicator, problem‑solver, and collaborative team player.
• Willing and able to travel up to 50% for on‑site monitoring visits across the West region; preference given to candidates residing in Los Angeles, Phoenix, Seattle, Denver, or Portland near major hub airports to support efficient regional travel.

What ICON Can Offer You

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to a competitive salary, ICON offers a range of additional benefits focused on well‑being and work‑life balance for you and your family.

Our Benefits Examples Include

• Various annual leave entitlements.
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a global network of over 80,000 independent specialized professionals who support you and your family’s well‑being.
• Life assurance.
• Flexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, and others.

At ICON, inclusion and belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If you require a reasonable accommodation for any part of the application process or to perform the essential functions of this position because of a medical condition or disability, please let us know or submit a request.

Salary

Salary range: $91,336.00–$114,170.00

Bonus, Compensation, Stock, Benefits & Disclaimer Verbiage

Actual compensation will be determined based on geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation, and commissions in some cases depending on your role and performance.