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Senior Clinical Research Associate

đŸ”„ 23 minutes ago

đŸ‡§đŸ‡· Brazil – Remote

⏰ Full Time

🟠 Senior

đŸ§Ș Clinical Research

đŸ—ŁïžđŸ‡Ș🇾 Spanish Required

Where this job comes from

Posted on PSI CRO AG's careers page, not through a job board

First seen by Remote Rocketship 23 minutes ago

Logo of PSI CRO AG

PSI CRO AG

1001 - 5000 employees

Founded 1996

đŸ„ Healthcare

đŸ’Œ 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

‱ Train, mentor, and supervise study-level responsibilities for junior CRAs ‱ 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 and feasibility research ‱ Serve as contact for clinical investigators, vendors, and support services regarding study progress ‱ Prepare and deliver presentations at Investigator 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

‱ College/University degree in Life Sciences or an equivalent combination of education, training & experience ‱ Full working proficiency in Spanish and English ‱ At least 3 years of independent on-site monitoring experience in Mexico ‱ Experience in all types of monitoring visits in Phase II and/or III ‱ Availability to travel ‱ Experience in Oncology or Infectious Diseases is a plus ‱ Proficiency in MS Office applications ‱ Ability to plan and work in a dynamic team environment ‱ Communication, collaboration, and problem-solving skills

đŸ–ïž Benefits

‱ Tailored courses and mentoring ‱ Career development opportunities ‱ Training, mentoring, and leadership development ‱ Opportunity to grow with the company

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

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