Remote Clinical Trial Job at ICON, Brazil | Life Sciences | Apply Now
If you are an early-career life scientist, a clinical trials coordinator, or a healthcare professional looking to transition your regional study knowledge into a massive global clinical monitoring matrix, this full-time role at ICON plc is an exceptional career move. Offered as a fully home-based position out of São Paulo, Brazil, this position places you directly inside the data monitoring and trial execution engine of top-tier pharmaceutical pipelines. For organized professionals searching for a high-impact Clinical Trial Job, this position (internally aligned with In-House Clinical Research Associate / IHCRA functionalities) provides direct operational ownership over site feasibility assessments, study tracking databases, and regulatory documentation checks. It serves as an elite operational milestone to advance a long-term ICON Career and stands out as a premier selection for anyone tracking a competitive Life Sciences Job with a strong work-life balance.
About The Company
ICON plc is a world-leading global Contract Research Organization (CRO) and healthcare intelligence powerhouse driven by a unified mission to accelerate the development of innovative medicines, medical devices, and diagnostic tools. Managing multi-center operations across North America, EMEA, and LATAM, ICON provides the critical infrastructure, centralized technology, and data tracking networks that help pharmaceutical innovators combat global diseases. This specific vacancy is hosted within ICON Strategic Solutions, operating under a highly collaborative Functional Service Provider (FSP) model. In this setup, you are embedded directly into a single, major global pharmaceutical sponsor’s internal study delivery infrastructure. This architecture allows you to focus exclusively on that sponsor’s specific clinical pipeline protocols, proprietary monitoring systems, and local regulatory files, while simultaneously enjoying the job security, global network, and comprehensive employee benefits provided by ICON.
Remote Clinical Trial Job – Key Responsibilities
The Clinical Trial Assistant / IHCRA functions as a vital central anchor for the trial lifecycle, working remotely to support field-based monitors and study managers to ensure absolute protocol compliance across investigational sites.
Your core trial execution, database auditing, and site coordination duties include:
- Trial Activity Execution: Assisting in the centralized planning, initiation, and daily execution of clinical trial activities across assigned Brazilian research sites.
- Feasibility & Selection Support: Conducting site feasibility assessments, collecting baseline metric surveys, and participating actively in local investigator site selection processes.
- Investigative Site Coordination: Coordinating closely with site staff and study coordinators to ensure continuous compliance with complex protocols, standard operating guidelines, and local ANVISA regulations.
- Progress & Data Monitoring: Monitoring study enrollment velocities, tracing sample data collection activities, and auditing databases to ensure data quality, completeness, and accuracy to advance this Clinical Trial Job.
- Dossier Documentation Review: Assisting in the preparation, review, quality checking, and uploading of essential study documents, regulatory greenlight binders, and monitoring reports.
- Cross-Functional Communication Tracking: Serving as a primary in-house communication bridge, tracking action items, and providing relevant trial updates to the broader Local Study Team to support your ICON Career.
Qualifications & Profile Requirements For Remote Clinical Trial Job
ICON seeks a systematic, proactive team player who demonstrates an uncompromised attention to data detail and thrives when managing multiple tracking tasks simultaneously.
- Required Academic & Experience Criteria:
- Educational Foundation: A completed formal Bachelor’s degree in a relevant field, such as Life Sciences (Biology, Biomedical Science, Pharmacy, Biochemistry) or Healthcare (Nursing, Medicine) to qualify for this premium Life Sciences Job.
- Experience Tier: Previous experience in clinical research, clinical trial administration, database tracking, or a related healthcare/laboratory field is highly preferred.
- Linguistic Mastery: Professional fluency in written and verbal English is mandatory to interact with global study teams, alongside complete fluency in Portuguese for site interactions.
- Core Competencies & Skills:
- Strong baseline understanding of clinical trial phases, trial documentation, and international Good Clinical Practice (GCP) guidelines.
- Exceptional organizational, task prioritization, and time management habits to navigate a fast-paced clinical operations environment.
- Strong written and verbal communication traits to coordinate effectively with diverse cross-functional teams and medical site stakeholders.
- Proficient command of digital workspace tools (including Microsoft Excel, Word, and document management systems).
In short, the Clinical Trial Assistant / IHCRA position at ICON is a definitive route to translating your life sciences background or clinical trial experience into a highly marketable global asset. Securing an appointment here allows you to move past localized laboratory circles and take direct, house-based operational charge of the feasibility profiles, data collections, and protocol checks that drive international clinical studies forward. If you reside in São Paulo, hold a qualifying healthcare or life sciences degree, and possess an analytical approach to data verification, apply today to secure this premier selection in a Clinical Trial Job, launch an exceptional ICON Career, and lock in this outstanding Life Sciences Job.
