Site Activation Specialist 1

Overview

The Site Activation Specialist supports country-level site activation activities for clinical research studies, working under moderate supervision to coordinate investigative sites, documentation, systems, and timelines.

What you'll do

• Serve as the single point of contact for assigned investigative sites and project stakeholders.
• Perform feasibility, site identification, study start-up, and site activation activities.
• Prepare, review, distribute, and quality-check site documents.
• Maintain project information in internal systems, databases, and tracking tools.
• Track document approvals, execution, and site progress against project timelines.
• Review site performance metrics and provide feedback to management.
• Support project planning and implement contingency plans when needed.

What you'll need

• Bachelor's degree in life science or a related field.
• Three years of clinical research or other relevant experience, or an equivalent combination of education, training, and experience.
• Three years of clinical research experience.
• One year of experience in a leadership capacity.
• Knowledge of applicable regulations, standard operating procedures, and work instructions.

Details

• Location: Bangalore, India.