Study Start-Up CRA

ICON Strategic Solutions; Argentina; Presencial; ARS 1.200.000 - 1.800.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Competitive benefits

Descripción de la vacante

ICON plc in Buenos Aires seeks a Study Start Up Clinical Research Associate to oversee startup activities, ensure protocol compliance, and support site teams across trials. You will monitor sites, perform visits, and coordinate with cross-functional groups to ensure accurate data capture and regulatory adherence.

The ideal candidate holds an advanced degree in life sciences, nursing, or medicine, is based in Buenos Aires, and demonstrates strong English and regulatory/start-up experience in

Formación

• Advanced degree required in life sciences, nursing, or medicine.
• Based in Buenos Aires.
• Advanced English required.
• Strong experience in Regulatory Affairs for start-up projects.
• Experience as a Clinical Research Associate with knowledge of trial processes.
• Proficiency in monitoring, data integrity, and site management with clinical trial software/tools.

Responsabilidades

• Monitor clinical trial sites to ensure adherence to protocol and GCP.
• Conduct site visits, assess performance, and resolve issues for trial success.
• Collaborate with cross-functional teams for timely data collection and reporting.
• Provide training to site staff to maintain high trial conduct standards.
• Build and maintain relationships with site personnel and stakeholders.

Conocimientos

Clinical Research

Regulatory Affairs (Start-up)

Site Management

Monitoring

Data Integrity

English Proficiency

Educación

Advanced degree in life sciences, nursing, or medicine

Descripción del empleo

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a Study Start Up CRA to join our diverse and dynamic team. As a Study Start Up CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.

What You Will Be Doing

• Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
• Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
• Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
• Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
• Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile

• Advanced degree in a relevant field such as life sciences, nursing, or medicine.
• Based in Buenos Aires.
• Advanced level of English.
• Strong experience in Relulatory Affairs for start up projects.
• Experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
• Strong experience in Relulatory Affairs for start up projects.
• Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.

What ICON Can Offer You

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our Benefits Examples Include

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here