Clinical Research Coordinator

Job not on LinkedIn

🕒 July 27

🇧🇷 Brazil – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 47%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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UniTriTeam

WebsiteLinkedInAll Job Openings

11 - 50 employees

Founded 2021

🏥 Healthcare

🤝 B2B

🎯 Recruiter

Healthcare • B2B • Recruitment

UniTriTeam is a healthcare services firm that helps healthcare and clinical research organizations scale efficiently and compliantly. The company provides clinical research support and operations services including global staff augmentation, eSource study design and maintenance, EDC data entry, e-regulatory services, patient recruitment, CTMS administration and integration, business intelligence and data analysis, and finance/accounting support. It also offers technology services (CTMS, Salesforce, Monday. com, HubSpot, SharePoint, NetSuite) and talent acquisition solutions such as embedded recruiting and placement services.

📋 Description

• Coordinate day-to-day clinical trial operations in a remote capacity, ensuring compliance with study protocols and regulatory guidelines. • Support and facilitate remote patient visits, including scheduling, documentation, and follow-up. • Patient Recruitment support to include inclusion/exclusion understanding and qualifying patients for studies via phone. • Maintain accurate and timely data entry in EDC and CTMS systems; manage query resolution. • Assist with regulatory document management and remote IRB submissions and updates. • Prepare for and participate in remote sponsor/CRO monitoring visits, audits, and inspections. • Serve as a virtual liaison with sponsors, CROs, and internal site teams. • Support study startup and closeout tasks, including remote collection and verification of essential documents. • Monitor visit schedules and ensure all subject documentation is complete and up to date.

🎯 Requirements

• 2+ years of experience in clinical research coordination or clinical operations. • Strong understanding of GCP, ICH, and FDA regulatory requirements. • Proficiency with CTMS platforms – CRIO or Clinical Conductor strongly preferred. • Fluent in English – both verbal and written communication required. • Comfortable working independently in a fully remote setting across multiple time zones. • Highly organized with strong attention to detail and documentation accuracy. • Proficient in Microsoft Office Suite and remote communication platforms (Zoom, Teams, etc.).

🏖️ Benefits

• Work with a mission-driven organization transforming the clinical research industry. • Fully remote work environment with global team collaboration. • Exposure to innovative research sites and a wide variety of protocols. • Professional development and growth opportunities. • Supportive and inclusive team culture.

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