Senior Clinical Research Associate – Hematology/Oncology

🔥 19 minutes ago

🇧🇷 Brazil – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 10%

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Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.

📋 Description

• Lead site qualification, initiation, monitoring, and closeout visits • Ensure alignment with study protocols, GCP, and regulatory requirements • Oversee site performance, data quality, and patient safety through monitoring and source document verification • Identify risks proactively and support protocol compliance • Build relationships with investigative sites and provide training, guidance, and ongoing support • Coordinate and review study documentation, regulatory submissions, investigator site files, and Trial Master File updates • Track study milestones, evaluate deliverables, and contribute to operational planning and execution • Serve as a Lead CRA on global studies • Coordinate monitoring activities and mentor and train less experienced CRAs • Facilitate resolution of data queries and review paper and electronic CRFs • Support timely and accurate study data collection • Contribute to study team and investigator meetings, bid defenses, monitoring plans, study-specific tools, and training materials • Travel to investigative sites approximately 6–8 days per month

🎯 Requirements

• Medical Doctor (MD) or Pharmacy degree with at least 5 years of CRA experience; or a four-year degree in a life science-related field with at least 4 years of CRA experience; or a two-year college curriculum/equivalent training, preferably in nursing or life sciences, with at least 5 years of CRA experience • Extensive knowledge of clinical research processes, GCP, ICH guidelines, FDA and/or EU regulations, and applicable local regulatory requirements • Experience independently managing site monitoring activities across the clinical trial lifecycle • Ability to function as a Lead CRA • Proficiency with Microsoft Office, IxRS platforms, and electronic data capture (EDC) systems • Ability to mentor and influence others • Fluency in the local language(s) required for assigned countries • Proficiency in spoken and written English • Candidates must reside within the territory and be based in Porto Alegre, Curitiba, or Sao Paulo • Ability to travel approximately 6–8 days per month

🏖️ Benefits

• Collaborative and inclusive work environment • Growth and career development opportunities • Learning and professional development opportunities • Home-based/remote work arrangement • Opportunity to serve as a Lead CRA • Mentoring and training opportunities • Opportunity to contribute to study planning, training, and operational excellence

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