Internal Clinical Research Associate

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🔥 0 minutes ago

🏄 California – Remote

🏄 California – Remote

💵 $72.5k - $145.1k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🔬 Research Analyst

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Stryker

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1941

⚕️ Healthcare Insurance

🧬 Biotechnology

Healthcare Insurance • Medical Devices • Biotechnology

Stryker is a global leader in medical technology, providing innovative products and services across the healthcare sector. With a presence in countries across the Americas, Asia Pacific, Europe, and the Middle East & Africa, Stryker offers a wide range of medical technologies, including orthopedic implants, surgical equipment, and advanced hospital devices. The company is committed to improving patient outcomes and healthcare efficiency. Stryker continues to expand its global reach, offering localized solutions to meet diverse healthcare needs worldwide.

📋 Description

• Support site identification, qualification, activation, monitoring, and closeout activities across clinical studies • Maintain Trial Master Files and essential study documents to ensure inspection readiness and regulatory compliance • Partner with clinical study teams to develop, review, and manage study documentation required for trial execution • Review and maintain informed consent forms, case report forms, and other study-related materials • Generate study newsletters and communications to support investigator sites and cross-functional stakeholders • Track and support study invoicing activities and maintain associated documentation • Create and maintain study metrics, reports, and dashboards to support clinical trial oversight and execution • Support clinical trial registration, audit preparation, data collection activities, and adherence to regulatory and Good Clinical Practice requirements

🎯 Requirements

• Bachelor’s degree in Life Sciences or a related scientific discipline • 0+ years of experience • Experience in clinical research, clinical trial operations, or clinical study administration (preferred) • Experience working under Good Clinical Practice (GCP) guidelines (preferred) • Experience using electronic clinical trial databases, clinical trial management systems, or related research platforms (preferred) • Experience supporting clinical trial audits, inspections, or regulatory submissions (preferred) • Experience with clinical trial registration platforms and study reporting activities (preferred)

🏖️ Benefits

• Health insurance • Retirement plans • Flexible work arrangements • Paid time off • Professional development