Job Summary
The position of Senior Clinical Research Associate in Oncology requires active engagement within the South Central region of the United States. This role is part of ICON Strategic Solutions, where you will benefit from a sponsor-dedicated framework, leveraging ICON’s extensive global knowledge and resources. As a key player in the largest Functional Service Provider (FSP) organization, you’ll contribute to fostering strong relationships with our numerous sponsor partners, ensuring the continuous delivery of professional service and stability.
Responsibilities
- Manage and oversee clinical trial activities to ensure alignment with protocols and regulatory standards.
- Monitor trial site performance, participant recruitment, and compliance throughout the study lifecycle.
- Collaborate with cross-functional teams to facilitate project success and uphold quality assurance.
- Provide training and guidance to junior staff and site personnel as necessary.
- Maintain up-to-date knowledge of clinical research trends and therapeutic areas relevant to oncology.
Qualifications
- Significant experience in clinical research, particularly in oncology or related therapeutic areas.
- Strong understanding of ICH-GCP guidelines and regulatory requirements applicable to clinical trials.
- Excellent communication skills and ability to work effectively with diverse teams.
- Detail-oriented with a capability to manage multiple projects and priorities efficiently.
- Bachelor’s degree in a relevant field; advanced degree is a plus.
