FSP - Regulatory and Start-up Specialist

BZL IQVIA RDS Brasil Ltda; São Paulo; Híbrido; BRL 40.000 - 60.000; Tempo integral

Resumo da oferta

A leading clinical research organization in São Paulo is seeking a Site Activation Specialist to manage feasibility and site activation tasks. You will prepare site documents, serve as a point of contact, and ensure compliance with regulatory requirements. The ideal candidate has a Bachelor's degree in Life sciences, 1-2 years of regulatory experience, and advanced English skills. This position offers a hybrid working model and involves collaboration with various teams.

Qualificações

• 1-2 years of experience in a regulatory role in a CRO or pharma (not sites).
• Experience with CEP/CONEP submissions and amendments.
• Familiarity with ANVISA requirements and submissions.

Responsabilidades

• Serve as a single point of contact for feasibility, site activation, and maintenance activities.
• Prepare and manage site documentation and review site documents.
• Track progress and ensure execution of required regulatory documents.

Conhecimentos

Advanced English skills

Communication skills

Teamwork

Formação académica

Bachelor's Degree in Life sciences or a related field

Descrição da oferta de emprego

Under moderate supervision, the Site Activation Specialist executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional, or country level. Prepares and manages 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.

Essential Functions

• With moderate oversight and supervision, serve 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. Requires advanced knowledge within a specific discipline typically gained through extensive work experience and/or education.

Qualifications

• Bachelor's Degree in Life sciences or a related field.
• 1-2 years of experience in a regulatory role in a CRO or pharma (not sites) and the following particular experience:
  • CEP/CONEP - initial submission for Main Site and remaining sites, amendments to Main Site and Remaining sites, notifications.
  • ICF - Review and adaptation of local requirements (Country customization).
  • ANVISA (MoH) - Initial DEEC Submission, Substantial Protocol Amendments, FAEC Update (Anvisa Clinical trial Form), annual study report (DEEC), Annual Safety Report (DDCM)
• Advanced level of English skills.
• Great communication skills and ability to work in a team.

This is a hybrid role.

Offices are located in Sao Paulo, SP.

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