Site Activation Specialist (for US sites) in Argentina or Brazil

IQVIA; São Paulo; Teletrabalho; BRL 80.000 - 120.000; Tempo integral

Resumo da oferta

A global healthcare provider is seeking a Site Activation Specialist to manage site activation and regulatory activities. The role requires a Bachelor’s Degree in Life Science and 1-3 years of related experience. You will work independently, coordinate documents, and communicate with investigative sites. This is a home-based position available in Brazil or Argentina, offering flexibility and the chance to work in a dynamic environment.

Qualificações

• 1 - 3 years’ prior experience in life sciences or similar.
• Ability to work independently to problem-solve collaboratively.
• Advanced level of English required.

Responsabilidades

• Execute feasibility, site identification, and site activation activities.
• Prepare and manage site documentation and contracts.
• Serve as a Single Point of Contact (SPOC) for assigned studies.

Conhecimentos

Problem-solving skills

Interpersonal communication

Organizational skills

Formação académica

Bachelor’s Degree in Life Science or related field

Descrição da oferta de emprego

Our Site Activation Specialists work under moderate supervision, executing the feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional, or country level. You will prepare and manage site documentation; reviews and negotiates site documents and contracts with sites and sponsors; maintains, reviews, and reports on site performance metrics; serves as the primary point of contact for investigative sites; tracks completion of appropriate documents for sites; ensures contracts are fully executed; and establishes project timelines.

• Serve as a Single Point of Contact (SPOC) to 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
• Update and maintain 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 questionnaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

• Bachelor’s Degree in Life Science or related field
• 1 - 3 years’ prior experience in life sciences or similar (or equivalent combination of education, training and clinical, healthcare and/or pharma experience) working with regulatory and start up activities is a must. Prior experience supporting US sites is highly valuated.
• Advanced level of English (you\'ll be working with North America on a daily basis)
• Ability to work independently to problem-solve collaboratively and to raise issues appropriately as needed
• Good interpersonal communication and organizational skills to establish and maintain effective working relationships with co-workers, managers and sponsors

Home based role, in Argentina or Brazil!

#LI-NRJ #LI-Remote

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 https://jobs.iqvia.com