Site Management Associate II

ICON Clinical Research; São Paulo; Presencial; BRL 120 000 - 180 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Global Employee Assistance Programme (

Life assurance

Country-specific benefits

Resumo da oferta

ICON plc is a world-leading healthcare intelligence and clinical research organization. ICON offers a collaborative, inclusive environment that fosters innovation and excellence in clinical development.

As a Site Management Associate II, you will support the management and monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP). You will coordinate monitoring activities, assist in regulatory documentation, collaborate

Qualificações

• Bachelor's degree in life sciences, healthcare administration, or clinical research.
• Experience in clinical research, site management, or monitoring.
• Strong organizational and project management skills.
• Excellent analytical and attention to detail.
• Exceptional communication and interpersonal skills.
• Willingness to travel about 25%.

Responsabilidades

• Coordinate monitoring activities at clinical trial sites.
• Assist in regulatory document preparation and review.
• Collaborate with cross-functional teams to support trial sites.
• Track site performance metrics and provide reports.
• Mentor junior staff and support development.

Conhecimentos

Site management

Monitoring

GCP compliance

Communication skills

Analytical skills

Organizational skills

Travel readiness

Formação académica

Bachelor's degree in life sciences / healthcare / clinical research

Descrição da oferta de emprego

Site Management Associate II

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.

As a Site Management Associate II at ICON, you will support the management and monitor of clinical trial sites by ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.

What You Will Do:

You will contribute to clinical research activities, taking responsibility for your deliverables and working collaboratively.

Key responsibilities include:

• Coordinating monitoring activities at clinical trial sites, ensuring adherence to study protocols and timely resolution of site-related issues.

• Assisting in the preparation and review of regulatory documents, ensuring all site activities are compliant with GCP and applicable regulations.

• Collaborating with cross-functional teams to facilitate effective communication and support for trial sites throughout the study lifecycle.

• Tracking site performance metrics, analyzing data, and providing reports to enhance site management efficiency.

• Participating in training initiatives and mentoring junior staff to support their development in clinical trial management.

Your Profile:

You will bring relevant clinical research experience, along with the following qualifications and skills.

Required qualifications and experience:

• Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research.

• Experience in clinical research, site management, or monitoring, with a solid understanding of clinical trial processes and GCP guidelines.

• Strong organizational and project management skills, with the ability to handle multiple priorities and deadlines.

• Excellent analytical skills and attention to detail, with a focus on maintaining high-quality standards.

• Exceptional communication and interpersonal skills, with the ability to build and maintain effective relationships with site personnel and cross-functional teams.

• Willingness to travel as required (approximately 25%)

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 (https://careers.iconplc.com/benefits) 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 (https://careers.iconplc.com/reasonable-accommodations)