Senior Surgical Device CRA – Central Region

ICON; Texas; On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Retirement planning options

LifeWorks Employee Assistance Program

Job summary

ICON Strategic Solutions is seeking a Senior Clinical Research Associate to lead site monitoring for surgical device trials in the Central Region. The role emphasizes independent work, travel (~60%), and driving quality and compliance across sites.

You will monitor sites, conduct visits, and collaborate with cross-functional teams to ensure accurate data collection and timely reporting, while training site staff and building strong relationships with investigators and study teams.

Qualifications

• Bachelor’s degree in Life Science, Physical Science, Nursing or Biological Science.
• 3–5 years CRA monitoring experience in CRO/pharma environments.
• 1 year of medical device monitoring experience preferred.
• Strong knowledge of FDA regulations and ICH/GCP guidelines.
• Strong problem-solving and communication skills.
• Willingness to travel approximately 60%.

Responsibilities

• Monitor trial sites for protocol, regulatory and GCP compliance.
• Conduct site visits to assess performance and resolve issues.
• Collaborate with cross-functional teams for data collection and reporting.
• Provide training to site staff and other CRAs on trial conduct.
• Build and maintain relationships with site personnel and stakeholders.

Skills

CRA monitoring

FDA regulations

ICH/GCP guidelines

Interpersonal skills

Verbal communication

Written communication

Travel readiness

Education

Bachelor’s degree in Life Science

Job description

ICON Strategic Solutions is seeking a Senior Clinical Research Associate to lead site monitoring for surgical device trials in the Central Region. The role emphasizes independent work, travel (~60%), and driving quality and compliance across sites.

You will monitor sites, conduct visits, and collaborate with cross-functional teams to ensure accurate data collection and timely reporting, while training site staff and building strong relationships with investigators and study teams.