Site Activation Coordinator

QHR IQVIA Zagreb d.o.o.

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Sofia, Bulgaria Until 8/22/2026 2+ years exp First posted June 8, 2026 Last posted June 8, 2026
Job description

Job Overview
Under general supervision, perform tasks at a country/region level associated with site activation activities in accordance with  applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include feasibility or maintenance activities.

Essential Functions
• Under general supervision, perform feasibility,  site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the  Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy, under guidance of senior staff.
• Prepare site documents, reviewing for completeness and accuracy.
• Inform team members of completion of regulatory contractual. and other documents for individual sites.
• Distribute completed documents to sites and internal project team members.
• Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.
• Review, track and follow up the progress, the approval and execution of required documents such as questionaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents.

Qualifications
• Bachelor's Degree Life science or related field Req
• With 2 years’ experience in a healthcare environment or equivalent combination of education, training and experience. Established individual contributor who works under general supervision. Delivers objectives that significantly impact results for a job area. Tasks are not typically routine, and may require applying discretion within broad operational boundaries and procedures. Problems faced are general and may require some analysis to resolve.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

About this role

Summary

Coordinate site activation activities, review documents, support project timelines, ensure compliance in clinical research

Job title

Site Activation Coordinator

Experience level

2 years

Minimum experience

2+ years exp

Industry

healthcare

Location requirements

Sofia, Bulgaria; remote work not specified

Salary

Not specified

Management role

No

Skills & keywords

Required skills

regulatory documentationproject managementclinical trialsattention to detailcommunication

Preferred skills

None specified

Specializations

site activationregulatory documentationfeasibilityproject managementhealthcare
Locations

Structured locations inferred from the posting.

Sofia, Bulgaria

Work arrangement unknown City
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