Clinical Research Associate

đŸ”„ 36 minutes ago

đŸ‡§đŸ‡· Brazil – Remote

⏰ Full Time

🟱 Junior

🟡 Mid-level

đŸ§Ș Clinical Research

Apply Now
Find Similar Remote Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Logo of ICON plc

ICON plc

10,000+ employees

Founded 1990

đŸ’Œ Consulting

đŸ„ Healthcare

📩 Logistics

Consulting ‱ Healthcare ‱ Logistics

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

📋 Description

‱ Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials. ‱ Ensure protocol compliance, data integrity, and patient safety throughout the trial process. ‱ Collaborate with investigators and site staff to facilitate smooth study conduct. ‱ Perform data review and resolution of queries to maintain high-quality clinical data. ‱ Contribute to the preparation and review of study documentation, including protocols and clinical study reports. ‱ Work in a sponsor-dedicated model supported by ICON’s global expertise.

🎯 Requirements

‱ Bachelor's degree in a scientific or healthcare-related field. ‱ Minimum of 2 years of experience as a Clinical Research Associate. ‱ In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. ‱ Strong organizational and communication skills, with attention to detail. ‱ Ability to work independently and collaboratively in a fast-paced environment. ‱ Willingness to travel as required (approximately 60%). ‱ Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

đŸ–ïž Benefits

‱ Competitive base salary and performance related incentives ‱ Health and wellbeing programmes including medical, dental, and vision coverage where applicable ‱ Retirement and pension plans ‱ Life assurance and disability coverage ‱ Employee assistance programmes and wellbeing resources ‱ Learning and development opportunities through structured training and career pathways

Apply Now

Similar Jobs

đŸ”„ 23 hours ago

Parexel

10,000+ employees

đŸ’Œ Consulting

đŸ„ Healthcare

📩 Logistics

Clinical Research Associate monitoring clinical trial sites for Parexel, a clinical development and healthcare research company. Managing site relationships, documentation, compliance, and study integrity.

đŸ—ŁïžđŸ‡§đŸ‡·đŸ‡”đŸ‡č Portuguese Required

🕒 6 days ago

Syneos Health

10,000+ employees

đŸ„ Healthcare

đŸ’Œ Consulting

📩 Logistics

Country Regulatory Specialist managing Brazilian clinical research regulatory submissions for Syneos Health. Coordinating ethics and regulatory authorities, timelines, compliance, and country intelligence remotely.

🕒 July 27

Indeed

10,000+ employees

🎯 Recruiter

đŸȘ Marketplace

đŸ‘„ HR Tech

Remote Clinical Research Coordinator managing clinical research operations for a global leader in staffing. Ensuring compliance and facilitating remote patient visits in clinical trials.

🕒 July 27

EDETEK Inc.

201 - 500

💊 Pharmaceuticals

🧬 Biotechnology

☁ SaaS

Clinical Data Manager managing EDETEK’s clinical trial data systems, documentation, testing, coding, and database integrity. Translating sponsor requirements into data management plans for high-quality clinical databases.