Clinical Site Management Associate II

ICON Strategic Solutions

Malaysia

On-site

MYR 60,000 - 90,000

Full time

9 days ago

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Job summary

ICON Strategic Solutions seeks a SMA II to support management and monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and GCP guidelines. You will contribute to clinical research activities, deliverables, and cross-functional collaboration.

Key responsibilities include coordinating monitoring, preparing regulatory documents, tracking site performance, and mentoring junior staff.

Qualifications

Bachelor's degree in life sciences, healthcare administration or clinical research required.
Experience in clinical research, site management, or monitoring with knowledge of GCP and study protocols.
Strong organizational and project management skills with ability to handle multiple priorities and deadlines.
Excellent analytical skills and attention to detail with focus on high-quality standards.
Exceptional communication and interpersonal skills for relationships with site personnel and cross-functional teams.
Willingness to travel as required (approximately 25%).

Responsibilities

Coordinating monitoring activities at clinical trial sites, ensuring adherence to study protocols.
Assisting in preparation and review of regulatory documents, ensuring compliance with GCP and regulations.
Collaborating with cross-functional teams to support trial sites throughout the study lifecycle.
Tracking site performance metrics, analyzing data, and providing reports to improve site management.
Participating in training initiatives and mentoring junior staff in trial management.