Clinical Research Job at IQVIA
IQVIA is hiring a Clinical Research Coordinator for a fixed-term, part-time position in Rio Branco, Acre, Brazil. This Clinical Research Job opportunity at IQVIA Careers provides hands-on experience in clinical trials, supporting investigators and research sites to ensure smooth study execution. Ideal for candidates with a life sciences or nursing background, this role provides valuable exposure to clinical research operations within a globally recognized healthcare intelligence company.
Job Details:
- Job Title: Clinical Research Coordinator
- Location: Rio Branco, Acre, Brazil (Field-Based)
- Employment Type: Full-Time Fixed Term
- Contract Duration: 6 months
- Working Hours: 24 hours per week
- Start Date: Immediate
- Job ID: R1523892
About the Company:
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The company accelerates the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide.
With a strong commitment to integrity, IQVIA maintains high standards in recruitment and operations, ensuring compliance, transparency, and professionalism across all clinical research activities.
Educational Requirements:
- Bachelor’s degree in Life Sciences
- Clinical or nursing background preferred
- Basic knowledge of clinical trials
- Previous experience as a Study Coordinator (SC) preferred
Key Responsibilities:
- In this Clinical Research Job, you should perform clinical tasks, including EKG and vital sign collection
- Verify and correct research study information on source documents
- Research queries and variances; provide feedback to site data collectors
- Accurately enter trial data into the Electronic Data Capture (EDC) system at IQVIA Careers
- Track visits and procedures in the Clinical Trial Management System (CTMS)
- Prepare and maintain study files
- Submit regulatory and ethics documentation on time as a Clinical Research Coordinator
- Schedule research subject visits and generate reports
- Provide administrative support, including reception and supply management
- Assist investigators to ensure smooth clinical trial operations
Skills Required:
- Understanding of clinical trial processes
- Strong attention to detail and data accuracy
- Ability to manage regulatory documentation
- Good organizational and administrative skills
- Effective communication and teamwork skills
- Ability to work independently in a field-based setting
- Availability to work part-time (24 hours/week) in Rio Branco
Benefits of the Clinical Research Job:
- Opportunity to work with a global clinical research leader
- Hands-on experience in clinical trial coordination
- Exposure to EDC and CTMS systems
- Career progression support within IQVIA
- Flexible working arrangement (part-time schedule)
- Valuable fixed-term experience in a growing healthcare sector
