17 publicaciones de empleo destacadas de program specialist en b (¡Están contratando!)

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- Tiempo completo
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FeverUp —Capital Federal, Buenos Aires
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Ruby Labs —Buenos Aires, Buenos Aires
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ExxonMobil —Capital Federal, Buenos Aires
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ExxonMobil —Capital Federal, Buenos Aires
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EY —Capital Federal, Buenos Aires
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サイネオス・ヘルス —Buenos Aires, Buenos Aires
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Project Svcs Lab QC Analyst

IQVIA -
Buenos Aires, Buenos Aires

Postulate ahora

Detalles del empleo

Tiempo completo

Descripción completa del empleo

Buenos Aires, Argentina | Full time | Home-based | R1558401

We are seeking Quality Control Analyst to join IQVIA Laboratories at Buenos Aires, Argentina.

We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development.

Job Summary:

Under general guidance, the Quality Control Analyst reviews and ensures adherence to study set-up processes and procedures during study start-up and amendment phases for global clinical research studies. This role performs quality control of laboratory documentation and database configurations, supports process excellence, and helps maintain consistent quality standards across the organization.

What You'll Be Doing:

Perform quality control reviews of laboratory specifications and related study documentation including LSDs, lab events, testing requirements, blood volume charts, toxicity charts, blinding charts, sponsor standards, and ICS documents
Review project databases against laboratory specification documents to verify accuracy, completeness, and protocol alignment
Collaborate with Set-up Managers, Set-up Specialists, and cross-functional teams to resolve quality findings and support study deliverables
Monitor and facilitate QC timelines to ensure client expectations and standard turnaround times are achieved
Analyze quality trends and contribute to training initiatives, process improvements, and quality metrics reporting
Participate in internal and external audits and ensure activities are performed in accordance with ICH E6 Guideline for Good Clinical Practice
Support the training, mentoring, and development of junior staff and QC team members

What We Are Looking For:

Bachelor’s Degree in a Science-related field
5 years of clinical or research industry experience; 3 year’s Set-up related and/or Project Management experience or Equivalent combination of education, training and experience
Demonstrated computer proficiency with Microsoft Office, IQVIA systems, and ELVIS
Experience reviewing project databases, laboratory specifications, and study set-up documentation within a regulated environment
Other equivalent combination of education, training, and experience may be accepted in lieu of degree

The Knowledge, Skills and Abilities Needed for This Role:

Understanding of medical and clinical research terminology and knowledge of Set-up Management processes
Strong organizational, time management, and prioritization skills with the ability to meet strict deadlines in a fast-paced environment
Excellent written and verbal English communication skills with the ability to build effective relationships with customers, stakeholders, managers, and colleagues
Strong technical aptitude and attention to detail for document control and quality metrics management
Ability to collaborate globally and contribute to continuous process improvement initiatives

What We Offer You:

We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.

To learn more about our benefits, visit IQVIA Benefits.

If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!

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.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

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program specialist empleos en b

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