Clinical Research Associate II
hace 3 semanas
As a leading global contract research organization (CRO), Fortrea is seeking a highly skilled Clinical Research Associate II to join our Oncology team. The successful candidate will be responsible for site management and monitoring of clinical studies, ensuring the protection of subjects and integrity of data.
Key Responsibilities
• Conduct site monitoring responsibilities for clinical trials according to Fortrea's Standard Operating Procedures (SOPs), ICH guidelines and GCP, including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visits.
• Prepare and implement project plans related to Clinical Monitoring responsibilities.
• Ensure the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to alongside applicable regulatory requirements.
• Safeguard data integrity by careful source document review, source document verification, query generation, and resolution against established data review guidelines on Fortrea or client data management systems.
Requirements
• Strong knowledge of clinical research regulations and guidelines, including ICH GCP and SOPs.
• Excellent communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Strong analytical and problem-solving skills.
What We Offer
• Competitive salary and benefits package.
• Opportunities for career growth and professional development.
• Collaborative and dynamic work environment.
• Recognition and rewards for outstanding performance.
How to Apply
If you are a motivated and detail-oriented individual with a passion for clinical research, please submit your application, including your resume and cover letter, to [insert contact information].
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