
Clinical Research Associate Role
2 weeks ago
Clinical Research Associate Role
Experience the fulfillment of a dynamic career in clinical research with our organization.
As a Clinical Research Associate, you will be responsible for conducting site visits, ensuring compliance with protocols, and verifying accurate data reporting.
- Conduct qualification, initiation, monitoring, and closeout visits to ensure compliance with approved protocols;
- Communicate effectively with medical site staff, including coordinators and physicians;
- Verify investigator qualifications, training, and resources, including facilities, laboratories, equipment, and staff;
- Verify subject eligibility and monitor adverse events and concomitant medications;
- Regulatory document review and investigational product accountability;
- Complete monitoring reports and follow-up letters, providing summaries of significant findings;
Our Offerings:
- A comprehensive CRA Training Program;
- Ongoing professional development and growth opportunities;
- A competitive compensation package and benefits;
- A supportive work environment and opportunity to make a difference in patient lives;
- A sense of purpose and fulfillment in your career.
Key Responsibilities:
- Qualification Visits: Conduct qualification visits to assess investigator suitability and feasibility.
- Monitoring and Closeout Visits: Perform on-site monitoring and closeout visits to ensure protocol compliance.
- Adverse Event Reporting: Verify and report adverse events, concomitant medications, and illnesses.
- Regulatory Compliance: Ensure adherence to regulatory requirements, SOPs, GCP, and applicable regulations.
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