CRA2 - FSP | Argentina

QPL IQVIA RDS Poland Sp. z o.o.; Buenos Aires; Remote; ARS 69,181,000 - 99,928,000; Full time

Job summary

IQVIA Inc. is seeking a Clinical Research Associate 2 (FSP) to work from home-based in the Buenos Aires region. You will train and develop to advance your clinical monitoring career with dedicated mentoring and structured reviews.

You will contribute to global projects with a regional travel remit and access to in-house technology. The role requires at least 2 years of on-site monitoring experience, an advanced level of English, and willingness to travel up to 50%.

Qualifications

• Bachelor's degree in health care or related field.
• Minimum 2 years on-site monitoring experience.
• Advanced English.
• Willingness to travel 50%.
• Located in Buenos Aires, Argentina.

Responsibilities

• Perform site selection, initiation, monitoring and close-out visits with proper documentation.
• Support the development of a subject recruitment plan.
• Establish regular communication and administer protocol and study training to sites.
• Evaluate quality and integrity of site practices and escalate issues as needed.
• Manage progress by tracking regulatory submissions, recruitment, CRF completion and data queries.

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.

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 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.

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.