**Job Title:** Oncology Clinical Research Associate (CRA II) **Location:** Paraíso, São Paulo (Hybrid/Field-Based) **Sector:** Clinical Research – Biotech Specialist CRO **About the Client:** I am currently partnering with a globally recognized, specialized Clinical Research Organization (CRO) that focuses exclusively on supporting the unique needs of the biotechnology sector. With a reputation for agility and a deep therapeutic focus, my client is looking to expand its monitoring team in Brazil to support high-impact oncology trials. **The Role:** As a CRA II, you will serve as the primary point of contact for clinical sites, ensuring the highest standards of data integrity and patient safety. This is a role for a monitoring professional who thrives in a fast-paced environment and is passionate about bringing innovative cancer treatments to market. **Primary Responsibilities:** * Manage the full lifecycle of site visits, including pre-study/selection, initiation, routine monitoring, and close-out, ensuring adherence to ICH-GCP and study protocols. * Partner with investigative sites to develop and implement effective patient recruitment and retention strategies. * Provide ongoing training to site staff regarding specific protocols and regulatory expectations. * Perform rigorous source data verification (SDV) and monitor the accuracy of Case Report Forms (CRFs). * Oversee the maintenance of the Trial Master File (TMF) and Investigator Site Files (ISF). * Identify and escalate quality issues or site performance trends to project leadership. * Manage site-level administrative duties, potentially including budget tracking and regulatory document collection. **Requirements:** * **Education:** Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related healthcare field. * **Experience:** A minimum of 1 year of independent, on-site monitoring experience. * **Therapeutic Expertise:** Proven experience monitoring **Oncology** trials is essential. * **Knowledge:** Deep understanding of local Brazilian regulatory requirements, GCP, and ICH guidelines. * **Mobility:** Willingness to travel to sites as required by the study protocol. * **Language:** Professional proficiency in English and Portuguese (written and verbal) is expected. **Why Join This Team?** This is an opportunity to work within a dedicated biotech-focused environment where your expertise in oncology will be directly applied to breakthrough research. My client offers a collaborative culture and the chance to work on complex, high-science protocols. **How to Apply:** If you are an experienced CRA looking to specialize further in the oncology space with a leading global partner, please submit your CV for a confidential discussion.