Role Description We are looking for highly driven Research Analysts who can identify companies actively hiring and generate high-intent business opportunities for our US healthcare recruitment practice. You will directly contribute to client acquisition and revenue generation. If you understand where to find hiring signals, decision-makers, and real opportunities, this role can be extremely rewarding. - Identify companies with active hiring needs (especially in US markets) - Source decision-makers (HR Heads, Talent Leaders, Founders, etc.) - Gather and verify contact details (Email / LinkedIn / Phone) - Use platforms like LinkedIn, Apollo, ZoomInfo, job boards, etc. - Deliver high-quality, structured lead data on a daily basis - Continuously improve lead quality based on conversion feedback Qualifications - Experience in lead generation / market research / recruitment research - Strong understanding of how hiring signals work (job postings, expansion, funding, etc.) - Ability to identify high-intent opportunities, not just bulk data - Familiarity with tools like LinkedIn, Apollo, ZoomInfo, etc. - Good communication and analytical thinking Requirements - Direct impact on revenue (not just support function) - Work closely with a US-based recruitment team - Learn how client acquisition works in international markets - Build a long-term, high-income skillset in opportunity identification Ideal Candidate - Someone who is hungry, consistent, and performance-driven - Not looking for fixed salary, but high earning potential - Can work independently and deliver daily output

Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today. TRIO is looking for a Clinical Research Associate to join our Monitoring Resource team. Reporting to the CRA Line Manager, this position will be a remote full-time freelance position based in Ireland. Responsibilities: - Performing data verification of source documents; - Conducting site visits, including pre-study, initiation, monitoring, and termination; - Confirming adherence to all FDA, ICH-GCP, and local regulations; - Ensuring implementation and compliance with FDA, and ICH-GCP guidelines - Participating in budget negotiation and follow-up where applicable - Assisting with data validation and query resolution - Mentoring junior team members as required - Ensuring the completion and collection of regulatory documents Qualifications: - A minimum of 2 years of monitoring experience in oncology trials - Experience monitoring in early-phase trials will be valued. - Completion of a science-related Bachelor’s degree - Excellent knowledge of medical terminology and clinical monitoring process - Strong ICH-GCPs knowledge - Experience with clinical trial information systems - Ability to travel up to 60% on average - Must be legally authorized to work in the country Prior to applying please review TRIO's Applicant Information Notice To support efficiency, TRIO may use limited AI tools during the candidate review process. All hiring decisions are made by people, not AI. To ensure fairness and an accurate understanding of your skills, we ask that candidates refrain from using AI tools or AI‑generated responses during interviews or assessments. We want the opportunity to get to know you and your experience. Teamwork · Passion · Integrity · Innovation

Support the development and implementation of research agendas, analyze data for actionable insights, and collaborate with various stakeholders to enhance program operations and inform strategic initiatives.

• Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports • Oversee integrity of the study and utilize problem-solving skills to promote rapport with the site and staff • Review the performance of the trial at designated sites, ensure the rights and well-being of human subjects are safeguarded and are in accordance with protocol • Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines, while also ensuring compliance with the approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and the applicable regulatory requirement(s) • Evaluate the quality and integrity of the reported data, site efficacy and drug accountability • Monitor the completeness and quality of Regulatory Documentation and perform site document verification