Clinical Research Associate

ICON Strategic Solutions; United States; On-site; USD 80,000 - 125,000; Full time

Job summary

ICON Strategic Solutions is seeking Clinical Research Associates for multiple openings across North America. Ideal candidates have 2+ years of on-site monitoring experience and are proficient in ICH-GCP guidelines. Responsibilities include site management, compliance monitoring, and patient safety oversight. This is a full-time position requiring strong communication and problem-solving skills.

Benefits

401(k)

Vision insurance

Medical insurance

Qualifications

• 2+ years on-site monitoring experience for CRA.
• 4+ years on-site monitoring for Sr. CRA.
• Experience across multiple therapeutic areas, ideally Oncology and Hematology.

Responsibilities

• Serve as primary contact between sites and sponsor.
• Conduct site visits, ensure compliance, and monitor safety.
• Collaborate with cross-functional teams.

Skills

Clinical Research

On-site Monitoring

ICH-GCP Guidelines

Communication

Problem Solving

Team Collaboration

Education

Bachelor’s degree in Life Sciences

Registered Nurse (RN)

Tools

CTMS

eTMF

Job description

Direct message the job poster from ICON Strategic Solutions

ICON has an ongoing need for Clinical Research Associates and currently has 37 open CRA/Sr. CRA positions across North America. If you are interested, please apply today.

Clinical Research Associate: 2 + years on-site monitoring experience

Senior Clinical Research Associate: 4+ years on-site monitoring experience

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 escalate 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:

• Currently working for a CRO or Pharmaceutical company with:
• Clinical Research Associate: 2 + years on-site monitoring experience
• Senior Clinical Research Associate: 4+ years on-site monitoring experience
• A graduate with a Bachelor’s degree in Life Sciences or equivalent, or a qualified RN
• Eligible to work in United States without visa sponsorship
• A clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry
• Experienced across multiple therapeutic areas, ideally including Oncology (Prostate Cancer, and Lung Cancer) and Hematology
• Proficient in ICH-GCP, local regulatory requirements, and clinical systems like 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 preference given to candidates residing near major HUB airports within these states to support efficient regional travel

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research

• Industries

  Pharmaceutical Manufacturing

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Inferred from the description for this job

401(k)

Vision insurance

Medical insurance

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