Clinical Trial Site Coordinator I (Hybrid)

ICON; Manila; Hybrid; PHP 420,000 - 640,000; Full time

Job summary

ICON Strategic Solutions is seeking a Clinical Trial Associate for an office-based, hybrid role in Makati. You will support site monitoring, ensure protocol adherence, and help manage regulatory compliance to enable efficient trial operations.

Ideal candidates bring a life sciences or clinical research background, strong organization, and collaborative communication skills to contribute to sponsor-dedicated studies with ICON’s global expertise.

Qualifications

• Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research.
• Some experience in clinical research, site management, or related administrative roles is preferred but not mandatory.
• Strong organizational skills and attention to detail, with the ability to manage multiple tasks effectively.
• Basic knowledge of clinical trial processes and regulatory requirements is a plus.
• Excellent communication and interpersonal skills, with the ability to work collaboratively within a team environment.

Responsibilities

• Assisting in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
• Supporting site management activities, including documentation preparation, data entry, and tracking site performance metrics.
• Collaborating with cross-functional teams to facilitate communication and address site-related issues effectively.
• Maintaining accurate records of site activities and contributing to the preparation of monitoring reports.
• Participating in training and development initiatives to enhance knowledge and skills in clinical trial management.

Skills

Clinical research

Site management

Regulatory compliance

Study protocols

Education

Bachelor's degree in Life Sciences/Healthcare/Clinical Research

Job description

ICON Strategic Solutions is seeking a Clinical Trial Associate for an office-based, hybrid role in Makati. You will support site monitoring, ensure protocol adherence, and help manage regulatory compliance to enable efficient trial operations.

Ideal candidates bring a life sciences or clinical research background, strong organization, and collaborative communication skills to contribute to sponsor-dedicated studies with ICON’s global expertise.