Senior Clinical Research Associate - Remote (Pacific Time)

Stryker Group; Fremont (CA); Remote; USD 90,000 - 160,000; Full time

Job summary

Stryker seeks a Senior Clinical Research Associate (CRA I) for our Neurovascular division. This is a remote, U.S.-based role with preference for candidates in the Pacific time zone and with about 50% travel to sites across the network.

The CRA will support clinical studies end-to-end, including site monitoring, documentation, and compliance, while collaborating with cross-functional study teams to ensure data integrity and regulatory adherence.

Qualifications

• Bachelor's level degree in science/healthcare required.
• 2+ years of relevant clinical research experience.
• Fundamental knowledge of GCPs, clinical study development process, and logistics.
• Ability to apply ISO, FDA and related guidelines toward documentation.

Responsibilities

• Perform site monitoring and site management through all phases of clinical study (site qualification, initiation, interim monitoring, closeout).
• Conduct site visits for all phases (qualification, initiation, monitoring, closeout).
• Ensure site compliance to protocol, regulations and guidelines.
• Ensure data integrity by verifying data in case report forms against source documents.
• Identify and address any noncompliance issues at sites.
• Collect and track regulatory documents, maintain TMF documentation and ensure accuracy.
• Communicate relevant updates to study core team.

Skills

GCP knowledge

FDA guidelines awareness

Documentation skills

Education

Bachelor's degree in science/healthcare

Job description

Stryker seeks a Senior Clinical Research Associate (CRA I) for our Neurovascular division. This is a remote, U.S.-based role with preference for candidates in the Pacific time zone and with about 50% travel to sites across the network.

The CRA will support clinical studies end-to-end, including site monitoring, documentation, and compliance, while collaborating with cross-functional study teams to ensure data integrity and regulatory adherence.