• Independently manage all aspects of monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close-out visits. • Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements. • Build strong site relationships, acting as a primary point of contact and ensuring high-quality data collection. • Identify and resolve site issues, escalating as needed to maintain trial integrity and patient safety. • Activities around regulatory affairs, site activation and study-startup.

China Research Analyst Location: Remote Clearance: None Required BluePath Labs is a fast-growing research and consulting company committed to solving complex problems for federal, state, and local government clients. We offer a range of professional, scientific, and technology services. Our specific areas of expertise include business consulting, research and data science, and technology integration. We are actively seeking a China Research Analyst to join our China Research Team. Work Description: The China Research Analyst will support and conduct research and translation projects related to China's military, technological development, foreign policy, and foreign influence. Responsibilities: The China Research Analyst will support tasks such as: - Translate Chinese-language primary sources of varying complexity into clear, accurate English for diverse clients and audiences. - Conduct extensive primary-source research using Chinese-language materials across multiple formats (e.g., official documents, media, technical publications, and other open-source content). - Analyze and synthesize findings with awareness of China's political, scientific, and economic landscape. - Independently leverage Chinese-language primary sources to answer specific research questions and support project deliverables. - Draft, edit, and deliver written research products and translated materials that are well-organized, audience-appropriate, and deadline-driven. Requirements: - Possess strong Chinese language skills, especially but not exclusively in reading - Experience in independent research using Chinese-language materials - Some experience with Chinese to English translation work - Able to work independently and meet deadlines with minimal supervision - Demonstrate careful attention to detail - Excellent organizational skills - Able to communicate information clearly and succinctly, in both written and verbal formats - US citizenship - A bachelor's degree Preferred experience: - Bachelor's or master's in a related field - Publication record on topics related to China - Experience with data analysis and/or visualization - Experience designing and working with large sets of data in multiple languages Benefits: BluePath Labs offers a comprehensive benefits package. Benefits include, but are not limited to: employer-sponsored healthcare plan, lifestyle & wellness reimbursement, Flexible Spending Account (FSA), tuition assistance, 401(k) with company match, and paid time off for vacation / sick leave, in addition to 12 holidays per calendar year. About BluePath BluePath Labs combines mission and business insights with advanced technologies to deliver measurable performance improvements for our clients. BluePath is dedicated to surpassing client expectations by always living by our core values of integrity, professionalism, and resilience. BluePath's extensive experience in Government, Military, Commercial, and Academic environments is unique among small businesses and a core differentiator of our solutions. Our multidisciplinary background allows us to solve diverse and complex problems. Most importantly, we work closely with our clients to frame problems correctly, optimize processes, leverage technologies, and implement enduring solutions. Labs are where ideas are born, experiments occur, and breakthroughs happen. It is the hallmark of BluePath's culture. https://www.bluepathlabs.com/ BluePath Labs is an equal opportunity employer.

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