Senior CRA

IQVIA; Buenos Aires; Presencial; ARS 1.800.000 - 3.000.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Senior Clinical Research Associate to oversee planning, execution, and management of clinical trials. Responsibilities include site visits, recruitment planning, protocol training, and ensuring data integrity and regulatory compliance.

The role requires strong organizational skills, ability to work independently, and travel as needed. Proficiency in CTMS/EDC and English language is essential.

Formación

• Bachelor's degree in a health care or science discipline or equivalent.
• At least 4 years of on-site monitoring experience.
• Advanced in English.
• Knowledge of GCP/ICH guidelines and regulatory requirements.
• Strong organizational and time management skills.

Responsabilidades

• Perform site selection, initiation, monitoring and close-out visits with proper documentation.
• Support development of subject recruitment plans.
• Establish regular communication and train sites on protocol and study procedures.

Conocimientos

On-site monitoring

GCP/ICH knowledge

Advanced English

CTMS proficiency

EDC proficiency

Independent worker

Team collaboration

Educación

Bachelor's degree in health care or sciences

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.

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.

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.