Senior CRA

IQVIA LLC; Buenos Aires; Presencial; ARS 1.500.000 - 2.100.000; Jornada completa

Descripción de la vacante

IQVIA LLC in Argentina is seeking a Senior Clinical Research Associate to oversee planning, execution and management of clinical trials. You will ensure data integrity, regulatory compliance and successful trial delivery across sites.

Responsibilities include site selection, initiation, monitoring, close-out visits, training site staff, and tracking submissions, recruitment, CRF completion, and data queries. Strong English and GCP knowledge are essential.

Formación

• Bachelor's degree in health care or a scientific discipline
• At least 4 years of on-site monitoring experience
• Advanced in English
• In-depth knowledge of GCP, ICH guidelines, and regulatory requirements
• Strong organizational and time management skills
• Excellent communication and interpersonal skills
• Ability to work independently and as part of a team
• Proficiency in CTMS and EDC systems
• Willingness to travel as required

Responsabilidades

• Perform site selection, initiation, monitoring and close-out visits with documentation
• Support development of a subject recruitment plan
• Provide protocol and study training to assigned sites
• Evaluate site practices and escalate quality issues
• Track regulatory submissions, recruitment, CRF completion, and data query resolution

Conocimientos

Communication

Time management

Independent worker

Team collaboration

Organizational skills

GCP knowledge

ICH Guidelines

CTMS

EDC

Travel flexibility

Educación

Bachelor's degree in health/science

Herramientas

CTMS

EDC

Descripción del empleo

The Senior Clinical Research Associate (CRA) will play a crucial role in the planning, execution, and management of clinical trials. This position requires a highly skilled and experienced professional who can ensure the integrity of clinical data, compliance with regulatory requirements, and the overall success of clinical research projects. While projects vary, your typical responsibilities might include:

• Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
• Supporting the development of a subject recruitment plan
• Establishing regular lines of communication plus administering protocol and related study training to assigned sites
• Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
• Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution

You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.

Requirements

• A Bachelor's degree in a health care or other scientific discipline or educational equivalent
• At least 4 years of on-site monitoring experience.
• Advanced in English.
• In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
• Strong organizational and time management skills.
• Excellent communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Willingness to travel as required.

If you want to make an impact in the global research market, where we are working to make a real difference in patient health. 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.