Sr Site Activation Specialist / Contract Specialist (Clinical Trials)

Location: Istanbul, Turkey

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Support country-level site activation, study start-up, and clinical trial agreement activities.
• Perform feasibility, site identification, start-up, and site activation activities in line with applicable regulations, SOPs, and work instructions.
• Act as a single point of contact for investigative sites, Site Activation Managers, project management, and other departments.
• Coordinate clinical trial submissions, distribute completed documents, and support study initiation timelines.
• Ensure the quality of deliverables, regulatory compliance, and adherence to project timelines.
• Support clinical trial contract and budget management activities.

Requirements

• For the Senior Site Activation Specialist position: a Bachelor's degree in Life Sciences or a related field.
• For the Contract Negotiator position: a Bachelor's degree in Law or a related field.
• At least 3 years of experience in clinical trial submissions, including Ministry of Health and Ethics Committee initial applications, or in clinical trial contracts.
• Experience in a CRO environment supporting multiple sponsors is preferred for the Site Activation Specialist position.
• Strong interpersonal, communication, and organizational skills.
• Ability to manage multiple projects and build effective relationships with colleagues, managers, sponsors, and investigative sites.

Culture & Benefits

• Exposure to studies across 21 therapeutic areas.
• Collaboration with a global team operating across 141 locations.
• Access to varied studies, projects, and innovative technologies.
• Collaborative work environment with opportunities for professional development.