Sr Site Activation Coordinator

PRT IQVIA RDS Spain, S.L – R.P. Portugal; Oeiras; Presencial; EUR 20 000 - 30 000; Tempo integral

Resumo da oferta

A leading global clinical research company is seeking a candidate in Lisbon, Portugal, to provide support in site activation and management of regulatory documentation for clinical trials. The successful applicant will coordinate activities and ensure compliance with all regulations, contributing to the success of innovative healthcare solutions. Strong organizational skills and effective communication are essential in this role.

Qualificações

• Experience in site activation and clinical trial agreements.
• Strong organizational and project management skills.
• Ability to communicate effectively with stakeholders.

Responsabilidades

• Identify and manage site regulatory documentation.
• Provide primary contact for investigative sites.
• Track completion of regulatory and contractual documents.

Descrição da oferta de emprego

Overview

Job Overview: Provides support to the different stakeholders in the organization to ensure the best possible outcomes.

Responsibilities

• Site identification and feasibility activities, regulatory, start-up, and maintenance activities
• Preparation, review, negotiation and management of site regulatory documentation and clinical trial agreements with sites and sponsors
• Maintains, reviews, and reports on site activation performance metrics
• Serves as the primary point of contact for investigative sites and/or sponsors
• Ensures tracking completion of all regulatory and contractual documents for sites
• Establishes project timelines
• Ensures all site activation activities are performed in accordance with all regulations, SOPs, work instructions and project requirements either at the global, regional, or country level and all relevant documents are submitted timely to the Trial Master File as per IQVIA/Sponsor requirements
• Establishes and/or executes goals and objectives for team(s) as well as tracking and delivering on operational/financial performance
• Participates in the broader Global Site Activation planning process; contributes to long- to mid-range goals and plans; and coordinates activities with other managers and their respective sub-families

About IQVIA

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.

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes.