CRA2 - Argentina

IQVIA; United States; Remote; USD 70,000 - 100,000; Full time

Job summary

IQVIA is seeking a CRA 2 - Homebased role to support site monitoring activities across global projects with a focus on quality and regulatory compliance. You will travel up to 50% and collaborate with diverse teams while developing your career through mentoring and quarterly performance reviews.

The role requires a healthcare or scientific degree and at least 2 years of on-site monitoring experience, along with strong English skills and the ability to work in a fast-paced, global environment.

Qualifications

• Bachelor’s degree in healthcare or other scientific discipline or equivalent
• At least 2 years of on-site monitoring experience
• Advanced English
• Willingness to travel ~50%

Responsibilities

• Perform site selection, initiation, monitoring and close-out visits with proper documentation
• Support 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
• Track regulatory submissions, recruitment, CRF completion, and data query resolution
• Collaborate and communicate with colleagues and customers

Skills

On-site monitoring

Advanced English

Education

Bachelor’s degree in healthcare or scientific discipline

Job description

CRA 2 - 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.