[Hiring] Staff Clinical Research Associate @Stryker
Role Description
Stryker is seeking a Staff Clinical Research Associate (CRA II) to join our innovative Neurovascular division. This is a remote, U.S.-based role offering meaningful growth opportunities for CRAs looking to deepen their clinical monitoring experience while supporting impactful clinical trials. The role includes approximately 50% travel, providing hands-on exposure and strong site partnership.
As Staff Clinical Research Associate, you will support clinical studies end-to-end, gaining experience in site monitoring, documentation, and compliance while working closely with cross-functional study teams.
What you will do
• Perform site monitoring and site management responsibilities through all phases of clinical study (e.g. site selection, site initiation, interim monitoring, and closeout)
• Conduct site visits for all phases (site qualification, site initiation, interim monitoring, and closeout)
• Ensure site compliance to clinical study protocol, applicable regulations and guidelines
• Ensure data integrity by verifying data in case report forms against source documents
• Identify and support site in addressing any noncompliance issues
• Collect and track regulatory documents, maintain trial master file (TMF) documentation and ensure accuracy
• Communicate relevant updates to study core team
Qualifications
• Bachelor's level degree or equivalent in science or health care field
• 4+ years of relevant clinical research experience
• Demonstrated independence in performing site monitoring (e.g. site selection, site initiation, interim monitoring and closeout visits) and site management activities
• Fundamental knowledge and good understanding of GCPs, clinical study development process, and logistics
• Ability to apply ISO, FDA and related guidelines toward documentation
Requirements
• Experience as a Clinical Research Coordinator, Clinical Trial Coordinator or Clinical Research Associate (Preferred)
• Experience in Device or Pharmaceutical industry (Preferred)
• CCRA Certification (Preferred)
Benefits
• Travel Percentage: 50%
• U.S. Pay Ranges:
• USN: $95,700 - $159,500 USD Annual
• US5: $100,500 - $167,500 USD Annual
• US10: $105,300 - $175,500 USD Annual
• US15: $110,100 - $183,400 USD Annual
• US20: $114,800 - $191,400 USD Annual
• US30: $124,400 - $207,400 USD Annual
Apply tot his job
Apply To this Job
Stryker is seeking a Staff Clinical Research Associate (CRA II) to join our innovative Neurovascular division. This is a remote, U.S.-based role offering meaningful growth opportunities for CRAs looking to deepen their clinical monitoring experience while supporting impactful clinical trials. The role includes approximately 50% travel, providing hands-on exposure and strong site partnership.
As Staff Clinical Research Associate, you will support clinical studies end-to-end, gaining experience in site monitoring, documentation, and compliance while working closely with cross-functional study teams.
What you will do
• Perform site monitoring and site management responsibilities through all phases of clinical study (e.g. site selection, site initiation, interim monitoring, and closeout)
• Conduct site visits for all phases (site qualification, site initiation, interim monitoring, and closeout)
• Ensure site compliance to clinical study protocol, applicable regulations and guidelines
• Ensure data integrity by verifying data in case report forms against source documents
• Identify and support site in addressing any noncompliance issues
• Collect and track regulatory documents, maintain trial master file (TMF) documentation and ensure accuracy
• Communicate relevant updates to study core team
Qualifications
• Bachelor's level degree or equivalent in science or health care field
• 4+ years of relevant clinical research experience
• Demonstrated independence in performing site monitoring (e.g. site selection, site initiation, interim monitoring and closeout visits) and site management activities
• Fundamental knowledge and good understanding of GCPs, clinical study development process, and logistics
• Ability to apply ISO, FDA and related guidelines toward documentation
Requirements
• Experience as a Clinical Research Coordinator, Clinical Trial Coordinator or Clinical Research Associate (Preferred)
• Experience in Device or Pharmaceutical industry (Preferred)
• CCRA Certification (Preferred)
Benefits
• Travel Percentage: 50%
• U.S. Pay Ranges:
• USN: $95,700 - $159,500 USD Annual
• US5: $100,500 - $167,500 USD Annual
• US10: $105,300 - $175,500 USD Annual
• US15: $110,100 - $183,400 USD Annual
• US20: $114,800 - $191,400 USD Annual
• US30: $124,400 - $207,400 USD Annual
Apply tot his job
Apply To this Job