Real World Evidence - Associate Site Strategy Lead PCD

IQVIA; São Paulo; On-site; BRL 180,000 - 280,000; Full time

Job summary

IQVIA in São Paulo is seeking a Site Strategy Lead to guide data generation proposals and ensure study execution readiness during the pre- and post-award phases. You will coordinate with internal teams, manage timelines and budgets, and advocate for efficient site and patient engagement strategies across studies.

This role requires a life sciences background, GCP knowledge, strong communication in English, and the ability to work in a fast-paced environment.

Qualifications

• Life sciences educational background.
• Experience in clinical operations – monitoring processes, documentation, GCP standards.
• Knowledge of clinical research regulatory requirements (GCP/ICH).
• Knowledge of budgets and pricing tools.
• Strong analytical skills with ability to dissect budgets and negotiate prices.
• Strong verbal and written communication skills, including English.
• Results-driven with focus on excellence and quality.
• Excellent time management with ability to manage several projects.
• Strong team player and collaborator in a fast-paced environment.

Responsibilities

• Assist with overall project efficiency and adherence to timelines and financial goals.
• Turn study budget and strategy into action to make RWE studies more predictable and efficient.
• Act as single functional lead for Data Generation proposals (Site ID, Site & Patient Engagement, Site Management & Technology strategies).
• Partner with internal teams to identify Data Generation strategies that address study challenges.
• Serve as single point of contact on the study for pre- and post-award site strategy questions.

Education

Life sciences

Job description

Job Overview

The Site Strategy Lead (SSL) is integral to the development of our delivery strategies at the very early phase of proposal development, and is a key player in supporting the study specific requests for the Data Generation group from the clients in the request for proposal. The SSL is key in building the most efficient and effective scenario for study execution during our sales process. This global team is working closely with other functional unit leads, and having the ability to build a strong proposal that IQVIA is able to operationalize and execute. In addition to the pre-award support the team provides, the SSL is very involved in the post award phase early on, and will work with the assigned Clinical Operations Lead (COL) to ensure that the sold Data Generation strategy is passed on to the assigned study team.

Key Activities

• Assist with overall project efficiency and adherence to project timelines and financial goals.
• Assist with turning a study budget and strategy into action that make RWE studies more predictable, shorten timelines, improve data quality and provide innovative solutions to the clients.
• Act as a single functional lead for Data Generation proposals, covering Site ID, Site and Patient Engagement, Site Management and Technology strategies.
• Partners with internal teams to understand relevant challenges within a study and to identify the Data Generation strategies that can help meet these challenges.
• Serves as single point of contact on the study to answer pre and post award site strategy questions.

Qualifications

• Life sciences educational background
• Prior experience and knowledge of clinical operations – monitoring processes, documentation, GCP standards
• In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Knowledge of project budgets and the use of pricing tools.
• Strong analytical skills with ability to dissect budgets, negotiate prices with internal teams and understand the “big budget picture”.
• Strong verbal and written communication skills, including excellent command of English.
• Results-driven with focus on excellence and quality.
• Excellent time management skills, ability to manage several projects with overlapping deliverables & schedule.
• Strong team player and collaborator with ability to operate in fast-paced environment.

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

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)