CRA1

IQVIA; Buenos Aires; Hybrid; ARS 800,000 - 1,200,000; Full time

Job summary

IQVIA in Buenos Aires is seeking a Clinical Research Associate (CRA) to work on global projects with a regional travel remit. The role focuses on site visits, regulatory tracking, and quality oversight, with mentoring and quarterly reviews in place.

Ideal candidates have 2+ years of remote monitoring or study coordination experience, a health-care related Bachelor's degree, and strong English skills. Travel up to 50% is required, with growth opportunities within a leading global research firm.

Qualifications

• Bachelor's degree required in health care or scientific field.
• At least 2 years of remote monitoring or study coordination experience.
• Advanced English proficiency required.

Responsibilities

• Perform site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation.
• Support the development of a subject recruitment plan.
• Establish regular lines of communication and administer protocol training to assigned sites.
• Evaluate the quality and integrity of site practices— escalate quality issues as appropriate.
• Manage progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolution.

Skills

Remote monitoring experience

Study Coordinator

Advanced English

Education

Bachelor's degree in health care or related discipline

Job description

## CRA1Apply: Buenos Aires, Argentina: Full time: Posted Today: R1568731Whether you’re beginning or continuing your career as a CRA, 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 resolutionYou 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.**You should have:**-A Bachelor's degree in a health care or other scientific discipline or educational equivalent -At least 2 years of remote monitoring experience or as Study Coordinator. -Advanced in English.-Travel availability (50%) -Alternatively, you should have an equivalent combination of education, training and experience 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.comIQVIA 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.