Clinical Research Associate: Site Monitoring & Study Oversight

IQVIA LLC; Pasig; On-site; PHP 279,000 - 390,600; Full time

Job summary

IQVIA LLC in Pasig is seeking a Clinical Research Associate to perform monitoring and site management work to ensure compliance with study protocols. This role involves conducting site visits and ensuring adherence to regulations and guidelines.

The ideal candidate holds a Bachelor's Degree in a scientific discipline or healthcare, with skills in communication, problem-solving, and project management. This position provides an opportunity to contribute to clinical research efforts and improve patient outcomes.

Qualifications

• Bachelor's Degree in scientific discipline or healthcare preferred.
• Some organizations require completion of CRA training program or prior monitoring experience.
• Basic knowledge of Good Clinical Practice (GCP) and ICH guidelines.

Responsibilities

• Perform site monitoring visits including selection, initiation, monitoring, and close-out.
• Ensure adherence to study protocol and regulatory requirements.
• Manage the progress of assigned studies and maintain documentation.

Skills

Written and verbal communication skills

Time and financial management skills

Organizational skills

Problem-solving skills

Proficiency in Microsoft Word, Excel, and PowerPoint

Education

Bachelor's Degree in scientific discipline or healthcare

Tools

Laptop computer

iPhone

iPad

Job description

IQVIA LLC in Pasig is seeking a Clinical Research Associate to perform monitoring and site management work to ensure compliance with study protocols. This role involves conducting site visits and ensuring adherence to regulations and guidelines.

The ideal candidate holds a Bachelor's Degree in a scientific discipline or healthcare, with skills in communication, problem-solving, and project management. This position provides an opportunity to contribute to clinical research efforts and improve patient outcomes.