Senior Clinical Associate

ICON Strategic Solutions; Brasil; Presencial; BRL 120 000 - 180 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Annual leave

Health insurance

Retirement planning

EAP LifeWorks

Life assurance

Flexible country-specific benefits

Resumo da oferta

ICON plc is a world-leading healthcare intelligence and clinical research organization. As a Senior Clinical Associate in Brazil, you will oversee and support trial execution, ensuring the highest standards of quality, compliance, and efficiency.

You will lead on coordination tasks, collaborate across cross-functional teams, and oversee site management to maintain data integrity and regulatory adherence throughout studies.

Qualificações

• Bachelor's degree in a scientific or healthcare-related field.
• Extensive experience managing clinical trials and understanding regulatory requirements.
• Ability to manage multiple projects with strong organizational skills.
• Excellent communication and collaboration with diverse teams.

Responsabilidades

• Lead clinical coordination tasks with focus on quality and continuous improvement.
• Coordinate trial activities ensuring adherence to protocols and timelines.
• Oversee site management and monitoring for data integrity and compliance.
• Provide guidance to clinical staff and investigators on best practices and standards.
• Monitor trial progress, identify risks, and implement mitigation strategies.

Conhecimentos

Clinical coordination

Regulatory knowledge

Project management

Communication

Formação académica

Bachelor's degree in a relevant scientific discipline

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.

As a Senior Clinical Associate at ICON, you will oversee and support the execution of clinical trials, ensuring the highest standards of quality, compliance, and efficiency.

What You Will Do

You will lead on clinical coordination tasks requiring technical depth, with a focus on quality and continuous improvement.

Key Responsibilities Include

• Managing and coordinating clinical trial activities to ensure adherence to protocols, regulatory requirements, and project timelines.
• Collaborating with cross-functional teams to address clinical trial issues, optimize processes, and ensure the effective execution of studies.
• Overseeing site management and monitoring to ensure data integrity and compliance with study protocols.
• Providing guidance and support to clinical staff and investigators, ensuring adherence to best practices and regulatory standards.
• Tracking and reporting on trial progress, identifying potential risks, and implementing strategies to mitigate challenges.

Your Profile

You will have a strong foundation in clinical coordination, with the experience to work independently and guide others.

Required Qualifications And Experience

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• Significant experience in clinical trial management, with a strong understanding of clinical trial processes and regulatory requirements.
• Proven ability to manage multiple projects effectively, with strong organizational and problem-solving skills.
• Excellent communication and interpersonal skills, with the ability to collaborate effectively with diverse teams and stakeholders.
• Detail-oriented with a proactive approach to ensuring trial success and addressing clinical challenges.

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