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About the Role
The Clinical Research Coordinator - Site Activation is a critical member of our site activation team at IQVIA Argentina. This role involves performing 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 guidelines.
Key Responsibilities
- Perform feasibility, site activation, and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs, and work instructions.
- Review documents for completeness, consistency, and accuracy, under the guidance of senior staff.
- Prepare site documents, ensuring they are complete and accurate.
- 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 on the progress, approval, and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents.
Requirements
- Bachelor's Degree in Life Science or related field.
- 2 years' experience in clinical research or 6 months in regulatory submissions in clinical research.
- Fluent in conversational (reading and writing) English.
- 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.
