• Build and maintain strong relationships with German-speaking clients. • Retain and reactivate existing clients through regular communication. • Increase client deposits, trading activity, and lifetime value. • Understand client trading goals and provide ongoing account support. • Promote new products, campaigns, and trading opportunities. • Handle client objections professionally and effectively. • Maintain accurate CRM records and client notes. • Work closely with internal departments to ensure an excellent client experience. • Achieve individual and team KPIs.

- Empower adult learners to achieve their language goals - Conduct online classes available 24/7 - Foster an inclusive culture of bravery, curiosity and growth - Support students' learning journeys through teacher-led classes

Role Description DataForce by TransPerfect is looking for native English-speaking men aged 55 and older across the United States to participate in a paid voice-recording study to help improve speech recognition and voice assistant technology. No previous experience is required. - Using your smartphone, you'll record short wake-up phrases and scripted commands like those used with voice assistants. - The task is completed remotely from home and takes approximately 30 minutes. Qualifications - 55 years of age or older - Born and currently live in the United States - Native speaker of English (US) - Have a smartphone - Can complete the recordings in a quiet indoor environment Requirements - Participants in specific demographic groups to help develop bias-free technology that would represent everyone. Benefits - Earn $7 USD for every person you refer who successfully completes the study. - Currently looking for men aged 18–28, so feel free to share this opportunity with eligible friends and family.

• Build and maintain strong relationships with clinical trial sites to enhance the site and patient experience while supporting enrollment goals and key study milestones. • Serve as an ambassador for clinical development programs by engaging investigators, sites, and research networks and promoting awareness of the company’s clinical pipeline. • Conduct Monitoring Oversight Visits to evaluate the quality of CRA monitoring activities and assess site readiness for regulatory inspections. • Perform remote and on-site site qualification activities as needed to support efficient site selection. • Lead or support Site Initiation Visits (SIVs), Interim Monitoring Visits (IMVs), and Close-Out Visits (COVs) to co-monitor studies, onboard new CRAs, and provide hands-on training across oncology programs. • Review and approve monitoring visit reports generated by CRAs to ensure quality, completeness, and compliance. • Analyze site performance and Key Risk Indicator (KRI) metrics to identify emerging risks, drive issue resolution, and contribute to the ongoing enhancement of study and site risk assessment strategies. • Deliver training and re-training to CRAs and site personnel on GCP, protocols, study-specific procedures, vendor requirements, and other critical trial documentation. • Provide oversight and support for site management activities, serving as an escalation point for monitoring-related issues and ensuring effective implementation of Corrective and Preventive Action (CAPA) plans. • Ensure all sites maintain inspection readiness and support sponsor activities during regulatory inspections or audits. • Leverage CTMS and TMF systems to maintain accurate study documentation, ensure timely filing of essential documents, and conduct TMF reviews or audits as required. • Independently author, review, or contribute to Clinical Site Monitoring Plans and other monitoring-related documentation. • Drive continuous improvement initiatives by developing or refining SOPs, work instructions, job aids, templates, and monitoring tools. • Partner with stakeholders to optimize site selection, monitoring processes, oversight reporting, CTMS workflows, and EDC functionality through gap analysis, testing, and implementation of process improvements. • Establish and maintain effective working relationships with investigators, site personnel, study teams, and CRA partners to ensure successful study execution.