Senior CRA

IQVIA; Municipio de Esquel; Híbrido; ARS 1.000.000 - 1.500.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Senior Clinical Research Associate to lead planning, execution, and management of clinical trials. This role ensures data integrity, regulatory compliance, and successful trial outcomes across sites.

The candidate will monitor sites, support recruitment planning, train site staff, and track regulatory submissions while collaborating with diverse teams and stakeholders worldwide.

Formación

• Bachelor's degree in a health care or scientific discipline or equivalent.
• At least 4 years of on-site monitoring experience.
• Advanced English proficiency.
• Strong knowledge of GCP and 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.
• Experience with 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.
• Communicate protocol and study training to sites.
• Evaluate site practices quality and escalate issues as needed.
• Track regulatory submissions, recruitment, CRF completion, and data queries.

Conocimientos

On-site monitoring

English proficiency

Regulatory knowledge

Time management

Communication skills

Independent and team player

Travel willingness

CTMS experience

EDC experience

Educación

Bachelor's degree in health care or scientific discipline

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.

Typical Responsibilities

• 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, we ask you to apply now and join our team.

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