• Independent, proactive work to set up and monitor studies, complete reports and maintain documentation • Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions • Balancing sponsor generated queries • Taking responsibility for study cost efficiency • Preparation and review of study documentation and feasibility studies for new proposals • Potential to assist in training and mentoring fellow CRAs

• Perform site management activities to support the client's Oncology site success and maintain a continuous state of inspection readiness • Act as the primary contact and facilitate efficient communications between the client's clinical trial team and the sites • Perform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits and Close-Out Visits) to ensure data integrity and subject safety in the client's trials • May perform oversight activities to assess monitoring quality and train/mentor less experienced CRAs • Promptly document monitoring activities and submit/approve visit reports • Manage site essential document collection and TMF reconciliation with site files • Support sites with local Institutional Review Board (IRB)/Ethics Committee (EC) submissions and confirm approvals • Regularly review site Key Risk Indicator (KRI) metrics, issues and action items to detect trends and ensure prompt resolution • Independently determine root causes and develop/implement site Corrective Action and Preventive Action (CAPA) plans • Deliver training to ensure sites comply with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs) and regulations • Support sites and the client's regulatory inspections • Contribute to site identification; drive site feasibility and qualification progress; and support site activation activities • Lead site engagement initiatives and foster relationships with key Oncology sites and networks

• Contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. • Collaborating with investigators and site staff to facilitate smooth study conduct. • Performing data review and resolution of queries to maintain high-quality clinical data. • Contributing to the preparation and review of study documentation, including protocols and clinical study reports.

Role Description - Curriculum structure discussion: Participate in designing lesson structures and instructional activities for assigned units - Courseware development: Finalize product design details and complete courseware production - Supporting materials development: Create pre-class, during-class, and post-class teaching support materials - Revision based on feedback: Adjust courseware logic and details of supporting materials promptly according to feedback - Content review and finalization: Conduct final content review to ensure logical consistency, accurate alignment with standards, and file finalization Qualifications - 3–5 years of frontline teaching experience in U.S. K–5 ELA - 3+ years of experience in ELA curriculum product development, with a track record of independently designing or deeply participating in reading and writing curriculum development - Familiar with Common Core ELA standards for reading and writing skills, as well as reading & writing classroom activity design - Proficient in major U.S. reading and writing instructional frameworks (e.g., Reader's Workshop, Writer's Workshop) - Clear and rigorous instructional logic, strong learning ability - Able to deliver curriculum products on time and with high quality Requirements - (At least one of conditions 1 and 2 must be satisfied) Benefits - Compensation: $20-$30 per hour - Job Type: Part-Time Company Description Think Academy is part of TAL Education Group (NY: TAL). TAL holds an esteemed reputation and influence in the education industry, standing as an industry leader with 20 years of technological and experiential accumulation. Joining Think Academy means becoming part of a global operation, with opportunities to learn the most cutting-edge and practical knowledge and skills. Headquartered in Beijing, China, Think Academy now operates in Hongkong China, US, UK, Canada, Singapore, Australia, Malaysia, and we are still expanding globally. As a crucial strategic business of TAL, Think Academy embodies an inclusive, pragmatic, and innovative corporate culture when expanding its global operations. Guided by a startup spirit from 0 to 1, it unites its people with shared beliefs, driven by mission, embracing responsibility, being open and honest, and giving it their all.