Senior CRA - Medical Device Trials (Midwest)

ICON Strategic Solutions; Kansas City (MO); On-site; USD 70,000 - 100,000; Full time

Benefits offered by this job

Competitive salary

Health and wellbeing programmes

Retirement and pension plans

Learning and development opportunities

Job summary

Ideal candidates have 2+ years of CRA experience, strong organizational and communication skills, and the ability to work independently while traveling up to about 60% of the time. Employment is contingent on right to work in the U.S.

Qualifications

• Requires a Bachelor’s degree in a scientific or healthcare-related field.
• Minimum 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.

Skills

Attention to detail

Communication skills

Organizational skills

Independent & collaborative

Education

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

Job description

Ideal candidates have 2+ years of CRA experience, strong organizational and communication skills, and the ability to work independently while traveling up to about 60% of the time. Employment is contingent on right to work in the U.S.