Life Sciences Job at ICON, Brazil | Site Management Associate | Apply Now
If you are looking to advance your career in clinical trial management from the comfort of a remote setting in Brazil, this Life Sciences Job as a Site Management Associate I (SMA I) at ICON plc is an excellent opportunity. This entry-to-mid-level Clinical Research Job provides a fantastic platform to build a long-term ICON career by directly supporting the operational efficiency and compliance of clinical trial sites.
About the Company
ICON plc is a world-leading healthcare intelligence and clinical research organization (CRO) dedicated to shaping the future of global clinical development. Operating a highly successful Functional Service Provision (FSP) model, ICON embeds its expert teams directly within client pipelines to drive innovation and excellence in drug and device development. The company is deeply committed to fostering an inclusive, diverse culture that rewards high performance and continuously nurtures internal talent. By joining ICON, you become part of a global mission to accelerate the delivery of safe, effective medical treatments to patients worldwide, supported by a vast network of clinical professionals, comprehensive employee wellness programs, and cutting-edge trial technologies.
Key Responsibilities
As a Site Management Associate I, your primary role is to deliver clinical research work to an exceptionally high standard, working closely with your immediate team and broader trial stakeholders to ensure site readiness and protocol adherence.
Your day-to-day duties will include:
- Site Monitoring Support: Assisting in the routine monitoring of clinical trial sites, ensuring strict adherence to approved study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
- Operational Administration: Supporting vital site management activities, which includes meticulous documentation preparation, accurate data entry, and tracking essential site performance metrics.
- Cross-Functional Collaboration: Collaborating actively with cross-functional teams to facilitate clear communication and address any site-related issues effectively and promptly.
- Record Keeping: Maintaining highly accurate records of all site activities and directly contributing to the preparation and finalization of site monitoring reports.
- Continuous Development: Participating in ongoing corporate training and development initiatives designed to enhance your foundational knowledge and skills in clinical trial management.
Qualifications & Skills Required For Life Sciences Job
This Clinical Research Job is designed for organized, detail-oriented professionals who already possess foundational experience in clinical studies and are ready to take on site management responsibilities.
- Educational Foundation: A Bachelor’s degree in a relevant field, such as Life Sciences, or Clinical Research, is required.
- Required Experience: Proven, hands-on experience supporting clinical research projects or clinical trial operations.
- Linguistic Fluency: An advanced level of English (both written and verbal) is required to communicate effectively with global teams and sponsors.
- Core Competencies: Strong organizational skills and a sharp attention to detail, paired with the ability to successfully manage and prioritize multiple tasks in a fast-paced environment.
- Location Profile: Must be based in Brazil (Role is aligned with the Sao Paulo hub).
Logistics, Compensation & Total Rewards
ICON understands that its success depends entirely on the quality of its people, offering a benefits package focused heavily on well-being and work-life balance.
- Location: Remote / Home-Based (Sao Paulo, Brazil).
- Work Format: Full-time, Functional Service Provision (FSP) model.
- Health & Insurance: A range of health insurance offerings to suit you and your family’s needs, alongside comprehensive life assurance.
- Financial Planning: Competitive retirement planning offerings designed to maximize your long-term savings.
- Well-being Support: Access to the Global Employee Assistance Programme (LifeWorks), providing 24-hour access to a network of over 80,000 independent professionals to support your family’s well-being.
- Additional Perks: Various annual leave entitlements and flexible country-specific optional benefits (such as childcare vouchers, discounted gym memberships, or health assessments).
In summary, this remote Site Management Associate I position is an exceptional stepping stone for clinical professionals based in Brazil. By securing this Life Sciences Job, you will master the mechanics of site monitoring and GCP compliance within a highly supportive, global CRO framework. If you have a background in clinical research support and an advanced command of English, apply today to secure this highly sought-after Clinical Research Job and begin a deeply rewarding ICON career.
