Senior Site Activation Coordinator
2 semanas atrás
IQVIA LLC is seeking a highly skilled Sr. Site Activation Coordinator to join our team. As a key member of our clinical research services team, you will be responsible for performing tasks related to contract and budget negotiation, working closely with sites from North America.
Key Responsibilities:- Under general supervision, perform feasibility, site activation, and maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs, and work instructions.
- 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 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.
- Bachelor's Degree in Life Science or related field.
- 1-2 years' experience in a healthcare environment or equivalent combination of education, training, and experience.
- Financial experience and a background in CRO or pharma (open to other industries as well).
- Good soft skills: communication, organization, attention to detail.
- Advanced level of English.
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.com.
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