Senior CRA – Surgical Medical Device Trials

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

Benefits offered by this job

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Life assurance

Flexible country-specific optional…

Job summary

ICON Strategic Solutions is seeking a Senior Clinical Research Associate for the Central Region to lead monitoring tasks with a focus on quality and continuous improvement. You will conduct site visits, ensure protocol adherence, and collaborate with cross-functional teams to ensure timely, accurate data collection and reporting.

The role requires a life science degree, 3–5 years of CRA monitoring experience (medical device monitoring preferred), and strong knowledge of FDA/ICH/GCP.

Qualifications

• Bachelor's degree in Life Science or related field.
• 3–5 years of CRA monitoring experience in CRO/pharma environments.
• Preferred 1 year of medical device monitoring experience.
• In-depth knowledge of FDA regulations and ICH/GCP guidelines.
• Strong interpersonal and communication skills.
• Willingness to travel approximately 60%.

Responsibilities

• Monitoring clinical trial sites to ensure adherence to study protocols and GCP standards.
• Conducting site visits to assess site performance and resolve issues.
• Collaborating with cross-functional teams to ensure accurate data collection and reporting.
• Providing training and guidance to site staff to maintain high trial conduct standards.
• Building and maintaining relationships with site personnel and stakeholders for smooth operations.

Skills

Clinical trial monitoring

FDA regulations

ICH/GCP guidelines

Communication skills

Problem solving

Travel readiness

Education

Bachelor's degree in Life Science

Job description

ICON Strategic Solutions is seeking a Senior Clinical Research Associate for the Central Region to lead monitoring tasks with a focus on quality and continuous improvement. You will conduct site visits, ensure protocol adherence, and collaborate with cross-functional teams to ensure timely, accurate data collection and reporting.

The role requires a life science degree, 3–5 years of CRA monitoring experience (medical device monitoring preferred), and strong knowledge of FDA/ICH/GCP.