Clinical Research Associate

🔥 17 minutes ago

🇧🇷 Brazil – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 10%

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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PSI CRO AG

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1996

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

PSI CRO AG is a global contract research organization (CRO) that specializes in conducting clinical trials. The company focuses on delivering pivotal Phase 2 and 3 clinical trials across various therapeutic areas, including Inflammatory Bowel Diseases, Oncology, Hematology, Infectious Diseases, Multiple Sclerosis, and Rare Diseases. PSI utilizes a proprietary technology platform for clinical trial planning and financial tracking to ensure trials are conducted on time and within budget. The company is recognized for its expertise, quality, compatibility, and reliability, having been awarded the CRO Leadership Awards for multiple consecutive years.

📋 Description

• Prepare, conduct, and report selection, initiation, routine, and closeout monitoring visits • Deliver training to investigators, site staff, and project teams • Work with complex studies • Perform CRF review, source document verification, and query resolution • Manage site communication • Participate in site identification • Serve as contact for clinical investigators, vendors, and support services regarding study progress • Participate in feasibility research • Prepare and deliver presentations at Investigator’s Meetings • Prepare for and attend company audits and resolve audit findings • Support Regulatory Affairs in procuring site regulatory documents • Maintain study-specific automated tracking systems

🎯 Requirements

• Only CVs in English will be considered • College/University Degree in Life Sciences • At least 2 years experience in patient care and/or health care or clinical environment • Full working proficiency in English • Experience in Clinical Research is a plus • Availability to travel • Proficiency in MS Office applications • Ability to plan and work in a dynamic team environment • Communication, collaboration, and problem-solving skills

🏖️ Benefits

• Tailored courses and mentoring • Career development opportunities • Opportunity to develop as a senior, trainer, mentor, and leader • Opportunity to advance toward future Lead Monitor roles

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