Senior Clinical Validation Analyst

Pharmaceutical Research Associates, Inc; Argentina; Presencial; ARS 81.610.000 - 108.814.000; Jornada completa

Descripción de la vacante

A leading clinical research organization is seeking a Senior Clinical Validation Analyst in Argentina. You will develop strategies for validating clinical trial data and work with cross-functional teams to ensure data integrity and compliance with regulations. The ideal candidate has an advanced degree and extensive experience in clinical data validation. Competitive salary and benefits are offered.

Servicios

Competitive salary

Diverse work culture

Work-life balance opportunities

Formación

• Extensive experience in clinical data validation.
• Strong understanding of regulatory requirements.
• Excellent communication and interpersonal skills.

Responsabilidades

• Develop and execute validation strategies for clinical trial data.
• Collaborate with teams to address data quality issues.
• Ensure compliance with regulatory and internal standards.

Conocimientos

Clinical data validation

Data analysis

Regulatory compliance

Project management

Stakeholder management

Educación

Advanced degree in life sciences, data science, or statistics

Herramientas

Validation tools and software

Descripción del empleo

Overview

As a Senior Clinical Validation Analyst you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

You will be partnering with one of the worlds premier Biopharmaceutical companies. Working across a vast portfolio of medicines and vaccines this company has, over centuries created a strong heritage of delivering innovative treatments and preventive medicines globally.

Responsibilities

What you will be doing:

• Developing and executing validation strategies and plans to ensure the accuracy and integrity of clinical trial data.
• Collaborating with cross-functional teams to identify validation requirements and address data quality issues.
• Overseeing the review and analysis of validation results to ensure compliance with regulatory standards and internal protocols.
• Providing strategic guidance on validation methodologies and improvements to enhance data reliability.
• Building and maintaining relationships with external partners and stakeholders to support validation efforts and drive best practices.

Qualifications

You are:

• Advanced degree in a relevant field such as life sciences, data science, or statistics.
• Extensive experience in clinical data validation, with a strong understanding of regulatory requirements and validation techniques.
• Strong analytical skills and proven ability to manage complex validation projects effectively.
• Expertise in data analysis and validation tools, with proficiency in relevant software and systems.
• Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive quality improvements within a complex organization.

What ICON can offer you:Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefitsAt ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. https://careers.iconplc.com/reasonable-accommodationsInterested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.