Sr Site Activation Coordinator
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Responsibilities
- Perform feasibility, site activation, and maintenance activities for investigative sites in assigned studies
- Support site start-up processes in compliance with regulatory requirements, SOPs, and study-specific guidelines
- Prepare, review, and manage site documentation, ensuring completeness, consistency, and accuracy
- Track and follow up on critical documents, including: Questionnaires
- Confidential Disclosure Agreements (CDAs)
- Regulatory and ethics submissions
- Informed Consent Forms (ICFs)
- Investigator Pack (IP) release documents
- Contract Negotiations & Budgeting
- Communicate status updates and document completion to internal teams and stakeholders
- Distribute finalized regulatory and study documents to sites and project team members
- Maintain and update internal systems, databases, tracking tools, timelines, and project plans with accurate information
- Collaborate effectively with cross-functional departments to ensure project timelines are met
Requirements
- ๐ Bachelor's degree in Life Sciences or a related field
- โ Minimum of 2 years' experience in a healthcare or clinical research environment (or equivalent combination of education, training, and experience)
- โ Strong understanding of clinical trial processes and site activation activities
- โ Ability to manage multiple tasks and timelines with attention to detail
- โ Proficient in working with internal systems, tracking tools, and documentation processes
- โ Strong organizational, analytical, and communication skills
- A proactive and collaborative team player who thrives in a dynamic environment
- An individual contributor who can work independently under general supervision
- Someone comfortable handling non-routine tasks and applying judgment within established procedures
- Problem-solver with the ability to analyze issues and drive resolution
Benefits
Additional Information
Senior Site Activation Coordinator ๐ Location: Athens, Greece - Hybrid ๐ Employment Type: Full-time Job Overview We are seeking a highly organized and detail-oriented Senior Site Activation Coordinator to support site activation activities across assigned studies. In this role, you will work under general supervision to ensure timely and compliant site start-up, in alignment with local and international regulations, SOPs, and project goals. You will collaborate closely with the Site Activation Manager (SAM), Project Management teams, and cross-functional stakeholders to drive efficient study start-up processes from feasibility through activation and maintenance.
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