10 publicaciones de empleo destacadas de staff data en microcentro, b (¡Están contratando!)

Sr. CRA (Unblinded)
ICON Plc —Buenos Aires, Buenos Aires
- Tiempo completo
1d
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Sr. CRA (Unblinded)

ICON Plc -
Buenos Aires, Buenos Aires

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Detalles del empleo

Tiempo completo
Hace 1 día

Descripción completa del empleo

Senior CRA (Unblinded)

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As a Clinical Research Associate (CRA) at ICON Plc , you will support and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards, with a focus on Unblinded studies .

What You Will Do:

You will perform clinical trial monitoring activities requiring technical expertise, with a focus on quality, compliance, and continuous improvement.

Key responsibilities include:

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 support and guidance to site staff 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:

You will have a solid foundation in clinical trial monitoring, with specific experience working on Unblinded studies .

Required qualifications and experience:

Bachelor's degree in a relevant scientific discipline or healthcare-related field.
At least 1 year of experience as a Clinical Research Associate working on Unblinded studies .
Strong understanding of clinical trial processes, monitoring practices, and regulatory requirements.
Proven ability to manage multiple sites and activities simultaneously, with strong organizational and problem-solving skills.
Excellent communication, interpersonal, and stakeholder management skills.
Oncology experience is highly desirable.
Willingness to travel as required (approximately 35% ), including occasional travel within LATAM .

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

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

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request .

Are you a current ICON Employee?

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