Medical Device Clinical Research Associate (Internal)

Stryker; Waltham (MA); On-site; USD 87,000 - 145,000; Full time

Job summary

Stryker in Waltham, MA is seeking an Internal Clinical Research Associate to support clinical studies from start-up to closeout. You will contribute to trial operations, device accountability, data review, and regulatory compliance to ensure adherence to quality standards.

Responsibilities include site qualification, monitoring, and closeout, device records maintenance, and creation of study communications for investigators and teams.

Qualifications

• Bachelor’s degree in Life Sciences required.
• 0+ years of experience in clinical research or related field preferred.

Responsibilities

• Support site qualification, activation, monitoring, and closeout across multiple studies.
• Manage investigational device accountability and inventory records.
• Maintain Trial Master Files and essential study documentation for inspection readiness.
• Review informed consent forms, case report forms, and related documents.
• Perform remote source data verification and study data review for quality and protocol compliance.
• Develop study metrics, reports, and dashboards to track progress and performance.
• Coordinate trial registration activities and support audit readiness.
• Create study communications and documentation for investigators and cross-functional teams.

Skills

GCP knowledge

Electronic trial databases

Clinical study coordination

Education

Bachelor’s degree in Life Sciences

Job description

Stryker in Waltham, MA is seeking an Internal Clinical Research Associate to support clinical studies from start-up to closeout. You will contribute to trial operations, device accountability, data review, and regulatory compliance to ensure adherence to quality standards.

Responsibilities include site qualification, monitoring, and closeout, device records maintenance, and creation of study communications for investigators and teams.