Site Management Associate II

A company is looking for an In-House CRA II.

Key Responsibilities

Coordinate monitoring activities at clinical trial sites, ensuring adherence to study protocols and timely resolution of site-related issues

Assist in the preparation and review of regulatory documents, ensuring compliance with GCP and applicable regulations

Track site performance metrics, analyze data, and provide reports to enhance site management efficiency

Required Qualifications

Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research

Experience in clinical research, site management, or monitoring, with a solid understanding of clinical trial processes and GCP guidelines

Strong organizational and project management skills, with the ability to handle multiple priorities and deadlines

Excellent analytical skills with a focus on maintaining high-quality standards

Exceptional interpersonal skills, with the ability to build and maintain effective relationships with site personnel and cross-functional teams