Site Contracts Associate, Mexico, IQVIA Biotech

IQVIA; Ciudad de México; Presencial; MXN 650.000 - 900.000; Jornada completa

Descripción de la vacante

IQVIA Biotech in Mexico City is seeking a Site Contracts Associate to support investigator grant estimates and site contracting for clinical trials.

This role focuses on developing budgets, templates, and documentation to ensure timely, compliant study start-up and ongoing trial activities, in collaboration with sponsors and regional teams.

Formación

• Bachelor's degree preferred in business, life sciences, or related field.
• Experience in budgeting, contracting, or site management is strongly preferred.
• Good understanding of clinical research processes and regulatory requirements.

Responsabilidades

• Develop investigator grant estimates and proposal text to support business development.
• Maintain contract and budget templates, systems, tools, and training materials.
• Collaborate with sponsors, regional teams to ensure contract delivery and compliance.
• Provide operational and financial contracting support for study start-up and maintenance.
• Assist in creation and review of documentation for start-up and trial activities.
• Contribute to contracting intelligence and performance reporting.
• Monitor contracting efficiency and timelines; report out-of-scope activities as needed.
• Ensure compliance with contract management and quality standards.
• Maintain accurate records in CTMS, databases, and project plans.

Conocimientos

Budgeting

Contracting

Site management

Regulatory knowledge

Educación

Bachelor’s degree in business or life sciences

Herramientas

Microsoft Office

Contract management systems

Descripción del empleo

Mexico City, Mexico

Full time

R1562525

IQVIA Biotech is hiring for Site Contracts Associate with 1-3 years' experience negotiating clinical site contracts and budget templates.

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.

Job Overview

We are seeking a Site Contract Specialist to support the development and execution of investigator grant estimates and site contracting activities for clinical trials. This role plays a critical part in ensuring timely and compliant study start-up and maintenance by managing financial and operational aspects of site contracts.

Essential Functions

• Develop investigator grant estimates and proposal text to support business development and proposal creation.
• Utilize and maintain contract and budget templates, systems, tools, and training materials for assigned sponsors, studies, or programs in alignment with the Scope of Work and Project Plan.
• Collaborate with sponsors, internal stakeholders, and regional/country teams to ensure successful delivery of project scope and compliance with sponsor requirements and RSU Management Plans.
• Provide specialized operational and financial contracting support to enable efficient trial initiation and maintenance while ensuring regulatory compliance.
• Assist in the creation and review of scientific, technical, and administrative documentation to support study start-up and ongoing trial activities.
• Contribute to the collection, analysis, and dissemination of contracting intelligence to support assigned studies and broader organizational needs.
• Monitor contracting efficiency and adherence to timelines and financial goals; report performance metrics and out-of-scope activities as needed.
• Ensure compliance with contract management and quality standards. Provide administrative and operational support to contract analysts, managers, and directors.
• Maintain accurate records in internal systems including CTMS, databases, tracking tools, and project plans.

Qualifications

• Bachelor’s degree in business, life sciences, or a related field preferred.
• Experience in clinical trial budgeting, contracting, or site management strongly preferred.
• Strong understanding of clinical research processes and regulatory requirements.
• Proficiency in Microsoft Office and contract management systems.
• Excellent organizational, analytical, and communication skills.

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.

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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