Clinical Research Associate II - Travel-Heavy, Data-Driven

ICON San Antonio; Los Angeles (CA); On-site; USD 70,000 - 100,000; Full time

Job summary

ICON Strategic Solutions in Denver is seeking a Clinical Research Associate II to design and monitor trials in a sponsor-dedicated environment, contributing to data integrity and patient safety.

You will conduct site qualification, initiation, monitoring, and close-out visits, collaborate with investigators, review data, and help prepare study documents. Willingness to travel up to 60% is required. This role sits within ICON's global network offering stability and growth.

Qualifications

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Strong organizational and communication skills, with attention to detail.
• Ability to work independently and collaboratively in a fast-paced environment.
• Willingness to travel as required (approximately 60%).

Responsibilities

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports.
• You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.

Skills

Communication skills

Organization

Attention to detail

Independence

Team collaboration

Travel up to 60%

Education

Bachelor's degree in a scientific or healthcare-related field

Job description

ICON Strategic Solutions in Denver is seeking a Clinical Research Associate II to design and monitor trials in a sponsor-dedicated environment, contributing to data integrity and patient safety.

You will conduct site qualification, initiation, monitoring, and close-out visits, collaborate with investigators, review data, and help prepare study documents. Willingness to travel up to 60% is required. This role sits within ICON's global network offering stability and growth.