CRA2 - FSP | Argentina

IQVIA; Tandil; Remote; ARS 1,000,000 - 1,500,000; Full time

Job summary

IQVIA in Argentina invites a CRA 2 (FSP) to join our global clinical research team from a homebased location. You will receive training, mentoring, and quarterly reviews while working on diverse projects with regional travel requirements.

Responsibilities include site visits, recruitment planning support, protocol training, quality evaluation, and tracking submissions and data queries. Fluent English and 2+ years on-site monitoring with travel readiness are essential.

Qualifications

• Bachelor's degree in a health care or scientific discipline or equivalent.
• Minimum 2 years of on-site monitoring experience.
• Proficiency in English is required.
• Ability to travel up to 50%.

Responsibilities

• Conduct site visits: selection, initiation, monitoring, close-out and documentation.
• Support the development of a subject recruitment plan.
• Communicate regularly and administer protocol training to sites.
• Evaluate site practices for quality and integrity and escalate issues.
• Track regulatory submissions, recruitment, CRF completion and data queries.
• Collaborate effectively with colleagues and have basic regulatory knowledge.

Skills

Advanced English

Education

Bachelor's degree in health care or related field

Job description

CRA 2 (FSP) - Homebased

This role is an ideal stepping-stone. You’ll have training and development to plan and progress your career in the direction you choose. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards.

Award winning and innovative, we’ll give you access to cutting-edge in-house technology, allowing you to work on global projects but with a regional / home state travel remit, so no need for national travel in certain countries. You’ll be building a smart and flexible career with no limits.

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 2 years of on-site monitoring experience (Mandatory)
• Advanced in English.
• Availability to travel (50% of time)
• Located in Buenos Aires, Argentina.
• Alternatively, you should have an equivalent combination of education, training and experience

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.