Sr Site Activation Coordinator
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Job Summary
Senior Site Activation Coordinator
Location: Athens Greece - Hybrid
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 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.
Key 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
Qualifications
- Bachelors degree in Life Sciences or a related field
- Minimum of 2 years experience in a healthcare or clinical research environment (or equivalent combination of education training and experience)
- Strong understanding of clinical trial processes and site activation activities
- Ability to manage multiple tasks and timelines with attention to detail
- Proficient in working with internal systems tracking tools and documentation processes
- Strong organizational analytical and communication skills
What Were Looking For
- 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
What We Offer
- Competitive compensation and benefits
- Flexible working options (depending on location)
- Opportunities for professional growth and development
- A collaborative global and inclusive work environment
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
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.
Required Experience:
Senior IC
About Company
IQVIA is the Human Data Science Company™. We are inspired by the industry we serve and provide solutions that enable life sciences companies to innovate with confidence, maximize opportunities and ultimately drive human health outcomes forward. Our approach is Human Data Science – a d ... View more
