Clinical Research Associate – Strykerย
Stryker is hiring a Clinical Research Associate (Internal), offering a fully remote role for candidates across the United States. This position is ideal for individuals with clinical research experience who want to support the administrative and operational aspects of clinical trials. Under the guidance of senior clinical staff, the CRA will assist in study start-up, documentation management, regulatory compliance, essential document collection, and maintaining inspection-ready clinical trial systems. Apply for the Remote Jobs at Stryker Careers Now!
Job Details:
- Position: Clinical Research Associate, Internal
- Work Type: Remote (US)
- Location: Virtual Address, CA 90002, US
- Company: Stryker
- Req ID: R554851
- Employee Type: Full Time
- Category: Clinical Affairs
- Travel: 10%
- Relocation: Not Available
- Salary Range: $79,500 โ $123,500 + bonus + benefits
About the Company:
Stryker is one of the worldโs leading medical technology companies, recognized for its award-winning work culture and commitment to advancing healthcare. Serving MedSurg, Neurotechnology, and Orthopaedics markets, Strykerโs products impact more than 150 million patients each year. The company offers a strong employee benefits package, professional development, and a values-driven mission to improve patient outcomes globally.
Educational Requirements:
- Bachelorโs degree in science, healthcare, or a related field.
- Minimum 2 years of clinical research experience.
Preferred backgrounds include:
- Clinical Research Coordinator (CRC)
- Clinical Trial Coordinator (CTC)
- Clinical Research Associate (CRA)
Key Responsibilities of the Clinical Research Associate Role:
- Maintain the Clinical Trial Management System (CTMS) and Trial Master File (TMF) in inspection-ready condition.
- Communicate with study sites to collect and review essential documents.
- Perform quality control (QC) checks on study files and resolve documentation issues.
- Support development, review, and maintenance of study documents and templates.
- Ensure adherence to GCP, regulatory standards, and internal policies.
- Assist with study start-up tasks, including site feasibility and initiation prep.
- Learn device-specific requirements: safety reporting, labeling, IFU tracking.
- Provide administrative and data entry support under supervision.
- Observe and support site monitoring visits with senior CRAs.
Skills Required for the Clinical Research Associate Role:
- Foundational knowledge of GCP and regulatory compliance standards.
- Experience in clinical research operations (CRA, CRC, CTC roles preferred).
- Strong administrative, documentation, and organizational skills.
- Ability to influence outcomes and work collaboratively with cross-functional teams.
- Proficiency in data entry and clinical systems.
- Excellent communication skills and attention to detail.
How to Apply?
Applicants interested for the Remote Jobs can apply directly through Strykerโs official careers website. Candidates may also sign up for job alerts to receive updates on future clinical research roles and remote opportunities.
