Internal Clinical Research Associate

Stryker seeks a Clinical Research Associate to support medical device clinical trial operations in Waltham, MA. The role involves study execution oversight, device accountability, documentation management, regulatory compliance, and coordination across multiple clinical studies from initiation through closure.

Responsibilities

• Support site qualification, activation, monitoring, and study closeout activities
• Manage investigational device accountability including inventory tracking and shipment coordination
• Maintain Trial Master Files and essential study documentation for regulatory compliance
• Perform remote source data verification and study data quality review activities
• Develop study metrics, reports, and dashboards to track operational progress

Requirements

• Bachelor's degree in Life Sciences or related scientific discipline
• Experience in clinical research or clinical trial operations (preferred)
• Knowledge of Good Clinical Practice (GCP) guidelines (preferred)
• Proficiency with electronic clinical trial databases or trial management systems (preferred)
• Experience supporting clinical trial audits or regulatory inspections (preferred)

Compensation: $87,000-$145,100 USD annual