Clinical Site Activation Pro – Start-Up

IQVIA; Singapore; On-site; SGD 65,000 - 95,000; Full time

Job summary

IQVIA LLC in Singapore is seeking a dedicated professional to manage feasibility, site activation, and related regulatory tasks within clinical research projects. You will coordinate with sites and sponsors, review and prepare essential documents, and monitor timelines under supervision.

The role emphasizes strong documentation review, adherence to SOPs, and collaboration with cross-functional teams to ensure compliant site activation and ongoing maintenance activities in a regulated environment.

Qualifications

• Bachelor's Degree Life sciences or a related field.
• 1-3 years’ clinical research or other relevant experience; or equivalent combination of education, training and experience.
• 3 years’ experience in a healthcare environment or equivalent combination of education, training and experience.

Responsibilities

• Serve as a Single Point of Contact (SPOC) to perform feasibility, site activation and some maintenance activities.
• Review documents for completeness, consistency and accuracy, under guidance of senior staff.
• Prepare and review site documents, ensuring regulatory and ethics approvals and IP release documents.
• Track completion of appropriate documents for sites and maintain project timelines.

Education

Bachelor's Degree Life sciences or a related field

Healthcare experience

Job description

IQVIA LLC in Singapore is seeking a dedicated professional to manage feasibility, site activation, and related regulatory tasks within clinical research projects. You will coordinate with sites and sponsors, review and prepare essential documents, and monitor timelines under supervision.

The role emphasizes strong documentation review, adherence to SOPs, and collaboration with cross-functional teams to ensure compliant site activation and ongoing maintenance activities in a regulated environment.