SrCRA1 - FSP | Argentina

IQVIA; Tandil; Presencial; ARS 92.241.000 - 153.735.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Senior Clinical Research Associate to lead on-site monitoring across clinical trials. The role focuses on data integrity, protocol training, and regulatory compliance, requiring strong communication and collaboration with diverse teams globally.

The successful candidate will bring at least 4 years of on-site monitoring experience, proficiency with CTMS/EDC systems, and an ability to travel as needed to study sites. IQVIA offers a dynamic, global environment.

Formación

• 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

Responsabilidades

• Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
• Supporting the development of a subject recruitment plan
• Establishing regular communication and training to assigned sites on protocol
• Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
• Managing progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolution
• Collaborating and communicating with a variety of colleagues and customers; basic knowledge of regulatory requirements

Conocimientos

Advanced English

Communication skills

Organizational skills

Time management

Teamwork

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.

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

You should have:

• 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.

About IQVIA

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

Integrity Statement

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.