Remote 3D Engineer: Real-Time Shaders & Gpu Pipelines

BairesDev; Quilmes; Remote; ARS 136,310,000 - 212,038,000; Full time

Job summary

IQVIA seeks a Real World Evidence - Associate Site Strategy Lead to drive site strategy during proposal development and ensure seamless post-award handoff to study teams. The role interfaces with Clinical Operations and Data Generation to optimize execution and quality.

The candidate will coordinate with global teams across multiple regions to deliver efficient, compliant study execution plans and innovative solutions for clients. English proficiency and strong budget analytics are essential.

Qualifications

• Life sciences background required.
• Experience with clinical operations: monitoring, documentation, GCP/ICH.
• Strong knowledge of regulatory requirements (GCP/ICH).
• Knowledge of budgets and pricing tools.
• Strong analytical skills for budgets and pricing.
• Excellent verbal and written English communication.
• Results-driven with focus on quality.
• Excellent time management and ability to manage multiple projects in fast-paced environment.

Responsibilities

• Support development of delivery strategies early in proposal phase.
• Assist in turning study budgets and strategy into actionable plans for RWE studies.
• Serve as single functional lead for Data Generation proposals: Site ID, Site & Patient Engagement, Site Management and Technology strategies.
• Partner with internal teams to identify challenges and Data Generation strategies to address them.
• Act as single point of contact for pre- and post-award site strategy questions.

Skills

Clinical operations

GCP/ICH knowledge

Budget awareness

Analytical skills

English communication

Time management

Team collaboration

Results oriented

Education

Life sciences background

Job description

Real World Evidence - Associate Site Strategy Lead

Bogota, Colombia
Mexico City, Mexico
Buenos Aires, Argentina
São Paulo, Brazil
Full time
R

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 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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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