Senior Clinical Research Associate

Stryker; United States; Remoto; USD 90.000 - 170.000; Tempo pieno

Descrizione del lavoro

Stryker is seeking 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 about 50% travel.

You will support clinical studies end-to-end, gaining experience in site monitoring, documentation, and compliance while collaborating with cross-functional study teams. Required is a bachelor’s degree in science or health care, 2+ years of clinical research experience, and knowledge of GCPs

Competenze

• Bachelor’s degree in science or healthcare field is required.
• 2+ years of clinical research experience.
• Fundamental knowledge of GCPs and regulatory processes.
• Ability to apply ISO/FDA guidelines to documentation.

Mansioni

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

Conoscenze

GCP knowledge

Clinical research experience

Regulatory compliance

Documentation skills

Formazione

Bachelor's degree in science/healthcare

Strumenti

CCRA Certification

Descrizione del lavoro

Work Flexibility: Remote

Stryker is seeking a Senior Clinical Research Associate (CRA I) to join our innovative Neurovascular division. This is a remote, U.S.‑based role with preference for candidates located in the Pacific time zone , 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 Senior 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

• Performsite monitoring and site management responsibilities through all phases of clinical study (e.g. site selection, site initiation, interim monitoring, and closeout)
• Conductsite visits for all phases (site qualification, site initiation, interim monitoring, and closeout)
• Ensuresite 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
• Communicaterelevant updates to study core team

What you need

Required

• Bachelor’s level degree or equivalent in science or health care field
• 2+ years of relevant clinical research experience
• Fundamental knowledge and good understanding of GCPs, clinical study development process, and logistics
• Ability to apply ISO, FDA and related guidelines toward documentation

Preferred

• Experience as a Clinical Research Coordinator, Clinical Trial Coordinator or Clinical Research Associate
• CCRA Certification
• Demonstrated independence in performing site monitoring (e.g. site selection, site initiation, interim monitoring and closeout visits) and site management activities

United States of America Pay Ranges:

• USN : $83,300 - $138,800 USD Annual
• US5 : $87,500 - $145,700 USD Annual
• US10 : $91,600 - $152,700 USD Annual
• US15 : $95,800 - $159,600 USD Annual
• US20 : $100,000 - $166,600 USD Annual
• US30 : $108,300 - $180,400 USD Annual
  View the U.S. work location and transparency guide to find the pay range for your location.

Travel Percentage: 50%

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.

Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.