Site Management Associate II

ICON Strategic Solutions; São Paulo; Presencial; BRL 90 000 - 150 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Health insurance

Pension/retirement planning

LifeWorks EAP

Life assurance

Flexible country-specific benefits

Resumo da oferta

ICON plc in Brazil is seeking a Clinical Research/Trial Manager to contribute to clinical research activities, taking responsibility for deliverables and working collaboratively.

You will coordinate site monitoring, support regulatory documents, and collaborate with cross-functional teams to optimize the study lifecycle. Travel about 25%.

This role offers an inclusive culture and competitive benefits.

Qualificações

• Bachelor’s degree in life sciences, healthcare administration, or clinical research.
• Experience in clinical research, site management, or monitoring with knowledge of GCP.
• Strong organizational and project management skills with ability to handle multiple priorities.
• Excellent analytical and attention to detail.
• Exceptional communication and interpersonal skills.
• Willingness to travel approximately 25%.

Responsabilidades

• Coordinate monitoring activities at clinical trial sites per protocol.
• Assist in regulatory document preparation and review, ensuring GCP compliance.
• Collaborate with cross-functional teams to support trial sites.
• Track site performance metrics and provide reports.
• Participate in training and mentor junior staff in trial management.

Conhecimentos

Clinical research experience

Site management

Monitoring

Communication skills

Travel flexibility

Formação académica

Bachelor’s degree in life sciences

Descrição da oferta de emprego

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.

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 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.