Clinical Trial Site Manager

A company is looking for a Site Management Associate 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

Collaborate with cross-functional teams to facilitate effective communication and support for trial sites throughout the study lifecycle

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

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