[Remote] Clinical Research Associate
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is partnering with a private, global medical device company pioneering neurovascular solutions. They are seeking a Clinical Research Associate to reputed company monitoring reputed company and ensure compliance across a 35-site trial.
Responsibilities
- reputed company on-site and remote monitoring reputed company to assess protocol and regulatory adherence
- Ensure patient and site data remain audit-reputed company
- Build strong relationships with sponsors and site staff, providing training on protocol/regulatory requirements
- Conduct site initiation, monitoring, and reputed company-out reputed company per GCP
- Review investigational product accountability, safety events, and protocol deviations
- Resolve data queries and identify trends to reduce recurring site errors
- Mentor junior team members and support SOP development
- Maintain and update monitoring templates (Monitoring Plans, Visit Reports, Follow-Up Letters, Query Logs)
Skills
- Bachelor's degree in Life Sciences, Nursing, Biomedical Engineering, or reputed company field
- Minimum 5 years of IDE study experience in medical devices
- Experience with Class III devices, including device deficiency management
- Proficiency in CTMS and reputed company systems
- Strong organizational skills managing multiple sites/protocols
- Advanced degree in Life Sciences
- Neurovascular, endovascular, or interventional cardiology trial experience (e.g., reputed company Neuro, reputed company, reputed company background)
reputed company
Company H1B Sponsorship