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Job summary
A clinical research organization is seeking a Clinical Research Associate (CRA) to ensure the successful execution of clinical trials. The candidate will conduct site visits, monitor compliance with regulatory standards, and manage clinical sites. Responsibilities include training site personnel, documenting site management activities, and ensuring data integrity. Candidates need a Bachelor’s degree and at least 1 year of on-site monitoring experience, with strong knowledge of GCP and ICH guidelines. The position offers a competitive salary range from $71,900 to $169,300 based on qualifications.
Qualifications
Requires at least 1 year of on-site monitoring experience.
Strong understanding of GCP, ICH guidelines, and regulatory requirements.
Ability to travel as required by the project.
Responsibilities
Conduct all types of site visits including monitoring and close-out.
Collaborate with site staff to implement subject recruitment strategies.
Deliver protocol and study-specific training to site personnel.
Monitor study progress and adherence to the protocol.
Document site management activities through detailed reports.
Skills
On-site monitoring experience
Understanding of GCP and ICH guidelines
Ability to travel
Education
Bachelor’s degree in life sciences or health-related field
Job description
A clinical research organization is seeking a Clinical Research Associate (CRA) to ensure the successful execution of clinical trials. The candidate will conduct site visits, monitor compliance with regulatory standards, and manage clinical sites. Responsibilities include training site personnel, documenting site management activities, and ensuring data integrity. Candidates need a Bachelor’s degree and at least 1 year of on-site monitoring experience, with strong knowledge of GCP and ICH guidelines. The position offers a competitive salary range from $71,900 to $169,300 based on qualifications.