Senior Clinical Research Associate-Hematology/ Oncology(Brazil)

Worldwide Clinical TrialsBrasilia, BrazilonsiteSalary not postedView the original posting at Worldwide Clinical Trials ↗

Join a global Contract Resource Organization (CRO) where innovation meets purpose. At Worldwide Clinical Trials , we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around the world. With more than 4,000 professionals across the globe, we foster a collaborative and inclusive environment where diverse perspectives are valued, growth is encouraged, and every contribution makes an impact. Whether you're building your career or bringing years of experience, you'll have the opportunity to learn, grow, and help shape the future of clinical research. Make an Impact as a Senior Clinical Research Associate) at Worldwide As a Senior Clinical Research Associate, you’ll play a key role in advancing clinical research by helping ensure studies are delivered with quality, compliance, and patient safety at the forefront. You’ll partner closely with investigative sites, sponsors, and study teams to support successful study execution from site qualification through closeout. You’ll take ownership of monitoring activities across multiple studies, helping protect data integrity, strengthen protocol compliance, and meet regulatory requirements. You’ll also have the opportunity to serve as a Lead CRA, mentor less experienced CRAs, and contribute to study planning, training, and operational excellence. Your expertise will support high-quality clinical trial delivery and, ultimately, the development of therapies that can make a meaningful difference for patients worldwide. Where You'll Work This is a home-based Clinical Research Associate role supporting sites across Brazil ( Curitiba / Porto Alegre / Sao Paulo). Candidates must reside within the territory to effectively support site visits and study activities. You will collaborate with sites, sponsors, and global study teams while traveling to investigative sites approximately 6-8 days per month. To best support our sites, we're seeking candidates who are based in Porto Alegre, Curitiba, or Sao Paulo. Travel will primarily be regional, with occasional travel to support sites in other locations as needed. What You'll Do Lead site qualification, initiation, monitoring, and closeout visits, ensuring alignment with study protocols, GCP, and regulatory requirements. Oversee site performance, data quality, and patient safety through effective monitoring, source document verification, and proactive risk identification. Build strong relationships with investigative sites, providing training, guidance, and ongoing support to promote protocol compliance and successful study delivery. Coordinate and review study documentation, regulatory submissions, investigator site files, and Trial Master File updates to maintain inspection readiness. Partner with project teams to track study milestones, evaluate deliverables, and contribute to operational planning and execution. Serve as a Lead CRA on global studies, coordinating monitoring activities and mentoring and training less experienced CRAs. Facilitate the resolution of data queries, review paper and electronic CRFs, and support timely and accurate study data collection. Contribute to study team and investigator meetings, bid defenses, monitoring plans, and the development of study-specific tools and training materials.} What You'll Bring Medical Doctor (MD) or Pharmacy degree with at least 5 years of CRA experience; 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. Demonstrated experience independently managing site monitoring activities across the clinical trial

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