Clinical Research Professional
4 days ago
Clinical Research Associates (CRAs) play a crucial role in the success of clinical trials. As a Senior CRA, you will oversee and manage the progress of clinical trials at investigational sites, ensuring adherence to study protocols, ICH-GCP, and local regulatory requirements.
About the Role:
This position requires a highly skilled individual with a strong understanding of oncology treatment modalities and protocols. You will conduct site initiation, monitoring, and close-out visits, offering continuous support to ensure optimal site performance. Your ability to establish and maintain strong working relationships with investigators, site staff, and other key stakeholders is essential.
Key Responsibilities:
* Oversee and manage the progress of clinical trials at investigational sites
* Conduct site initiation, monitoring, and close-out visits
* Ensure accurate and timely collection and reporting of clinical trial data
* Proactively identify potential risks and work with the study team to resolve issues affecting timelines, data quality, or compliance
* Provide guidance to junior CRAs and assist in their professional development
Requirements:
* A minimum of 2 years of experience as a Clinical Research Associate (CRA) in a clinical research environment
* At least 1 year of experience in oncology clinical trials, with a solid understanding of oncology treatment modalities and protocols
* In-depth knowledge of ICH-GCP, FDA, and other regulatory standards and guidelines
* Ability to travel to clinical sites as required by the study
Our Company:
i-Pharm Consulting is a global leader in healthcare data, technology, and advanced analytics, dedicated to supporting the pharmaceutical and biotechnology industries in the development of ground-breaking treatments.
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