Sr Site Activation Coordinator (North America Team) PCD

IQVIA; São Paulo; Teletrabalho; BRL 60 000 - 90 000; Tempo integral

Resumo da oferta

IQVIA is seeking a Site Activation Coordinator for a home-based role in Brazil. The position supports feasibility, site activation and regulatory document workflows across studies, aligning with SOPs and project requirements.

The candidate should have a Life Sciences degree with 2+ years CRO or 4+ years site experience, and an advanced level of English for communication with North American sites.

Qualificações

• Advanced level of English is mandatory.
• Regulatory/site activation tasks experience helps.

Responsabilidades

• Perform feasibility, site activation and some maintenance activities in studies under SOPs and guidance.
• Prepare site documents and review for completeness and accuracy.
• Inform team of completion of regulatory and other documents.
• Distribute completed documents to sites and project team members.
• Support updating internal systems, databases and project plans with accurate information.
• Review and follow up on progress, approvals and execution of regulatory, ethics, ICF and IP release documents.

Conhecimentos

English Advanced

Formação académica

Bachelor's Degree Life science or related field

Descrição da oferta de emprego

Job Overview

Under general supervision, perform 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/budgetary guidelines. May also include feasibility or maintenance activities.

Essential Functions

• Under general supervision, perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy, under guidance of senior staff.
• 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 the progress, the approval and execution of required documents such as questionaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents.

Qualifications

• Bachelor's Degree Life science or related field.
• With 2 years’ experience in a CRO or over 4 years of experience in a site, with previous experience in regulatory/site activation tasks.
• Advanced level of English is mandatory, you'll be in touch with sites from North America.

This is a home based role!

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.

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.

Vaga Exclusiva para Pessoa com deficiência (PCD)