Piedmont Healthcare
Site Specialist II
Georgia, Tbilisi · Mid · Contract
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About the role
- Inclusion and Accessibility ICON is an equal opportunity employer.
- If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Responsibilities
- We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
- Perform timely and accurate progress data entry of all documents collected from sites and of the relevant study site activation activities into the appropriate tracking systems and tools.
- Participate to internal study review meetings with study teams to provide updates on site progress in document collection and on the executed site activation tasks.
- Ensure accuracy and timely completeness of Trial Master File (TMF) documents submitted during start-up and perform a Quality Control (QC) review of files before transfer to maintenance for filing in TMF.
- Excellent organizational and project management skills, with the ability to prioritize and manage multiple tasks simultaneously.
Requirements
- Support coordination of all necessary translations required for any start-up documentation.
- Attend study team meetings as required
- Bachelor's degree in life sciences or a related field.
- Minimum of 2 years of experience in clinical research or regulatory affairs, with specific experience in study start-up activities.
- Strong understanding of regulatory requirements and guidelines for clinical trials, including ICH-GCP and local regulatory requirements.
Compensation
- Competitive base salary and performance related incentives
Benefits
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
- Visit our careers site to read more about the benefits ICON offers.
Company info
- As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
Equal opportunity
- ICON is an equal opportunity employer.
Visa & Work Authorization
- level critical documents and/or of site activation tasks required for site activation in accordance with ICON SOPs/WPs, Sponsor SOPs, applicable regulations/guidelines and the principles of ICH/GCP
This listing is sourced directly from Piedmont Healthcare's careers page and normalized into a canonical job model.