Senior Site Activation Specialist (Clinical Research)

Location: Prague, Czech Republic; hybrid

Company

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

What you will do

• Lead complex site activation projects and serve as the single point of contact for investigative sites, Site Activation Managers, project management, and other departments.
• Perform feasibility, site identification, study start-up, and site activation activities in line with regulations, SOPs, work instructions, and project timelines.
• Prepare, review, track, and follow up on site documents, questionnaires, regulatory and ethics submissions, informed consent forms, investigator packages, and contractual documentation.
• Coordinate completion of feasibility, regulatory, and contractual activities and provide local expertise during project planning.
• Perform quality control of documents, act as a subject matter expert, mentor junior specialists, and support sponsor-facing activities.

Requirements

• Bachelor’s degree in Life Sciences or a related field.
• 4–5 years of experience in clinical research, including at least 1 year in a leadership capacity.
• Experience with Ethics Committee and Regulatory Authority submissions, contract and budget negotiations, study start-up, and site activation.
• Knowledge of applicable functional and regulatory requirements, local regulations, SOPs, and ICH/GCP.
• Strong problem-solving, negotiation, communication, and multitasking skills.
• Native-level Czech and advanced English proficiency required.

Culture & Benefits

• Work within a global Global Site Activation team of approximately 2,000 employees.
• Collaborate with internal and external customers to support access to safe and effective clinical trial treatments.
• Opportunities for career development through innovation and the adoption of new technologies.
• Full-time hybrid working arrangement.