Role Overview - Hydra Host is looking for a Execution Analyst, Digital Infrastructure Finance, to sit at the intersection of our sales and financing functions. This role supports the sales team through the full pre-sale cycle - building financial models, building pitch decks, structuring GPU rental contract scenarios, and translating complex infrastructure economics into clear, compelling proposals for prospective clients. - This is a high-visibility role for someone early in their career who is commercially minded, financially rigorous, and genuinely excited about AI compute infrastructure. Responsibilities - Build and maintain financial models for GPU rental contracts, including multi-year pricing scenarios, utilization assumptions, and ROI analyses for prospective clients - Partner with the sales team to respond to financial, commercial, and transaction questions during the pre-sale process. - Develop client-facing materials that communicate contract economics, cost comparisons, and payback analysis in a clear and accessible format - Maintain and improve standardized modeling templates to support a repeatable, scalable sales process - Research GPU hardware specifications, market pricing, and competitive positioning to inform deal structuring - Collaborate with finance and operations teams to ensure models reflect accurate cost inputs and contract terms Qualifications - 1–3 years of experience in financial analysis, investment banking, corporate finance, or a related field - Strong Excel and financial modeling skills; comfort building models from scratch - Familiarity with GPU hardware, AI/ML infrastructure, or cloud compute economics is a strong plus - Ability to communicate financial concepts clearly to both technical and non-technical audiences - High attention to detail and comfort working in a fast-moving, deal-driven environment - Bachelor's degree in Finance, Economics, or a related field preferred Salary: 80000 - 130000 USD Per annum

Discover Your Career at Emory University Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future. We welcome candidates who can contribute to the excellence of our academic community. Description KEY RESPONSIBILITIES: - This individual will work as a Research Assistant under Prof. Stephen D. O'Connell in the Department of Economics. Responsibilities include literature review, data analysis, and presentations. Weekly meetings as well as ad hoc coordination meetings will also be expected. Research Assistant — Duties This is a half-time position supporting a mixed-methods study of livelihoods policy and social cohesion in post-conflict Iraq, conducted in partnership with the International Organization for Migration (IOM). The RA works under the supervision of PIs O'Connell (Emory) and Masterson (UCSB). Instrument Development - Lead the design of a semi-structured qualitative interview guide, drawing on preliminary findings from the project's large-scale randomized controlled trial (midline survey data covering ~6,000 participants) - Develop interview probes targeting specific quantitative results — both strong treatment effects and null findings — to elicit narratives about mechanisms, spillovers, and unintended consequences - Coordinate translation of the guide into Arabic and Kurdish, manage back-translation for accuracy, and incorporate feedback from piloting Fieldwork Preparation and Support - Help develop the sampling frame: purposive selection of ~150 participants across treatment/control groups, community types (IDP, returnee, host), gender, and geography - Prepare training materials for local enumerators and translators on ethical interviewing, confidentiality, and data quality - Support PIs during in-country fieldwork trips (January–April 2026), including logistics coordination and real-time quality checks on incoming interview data Analysis - Manage transcription and translation workflow for audio-recorded interviews - Conduct thematic coding of interview transcripts using qualitative analysis software, applying both inductive and deductive approaches - Integrate qualitative findings with quantitative RCT data to identify mechanisms and sources of treatment effect heterogeneity - Prepare tables, summaries, and narrative write-ups for use in the academic manuscript and policy brief Other - Assist with IRB/ethics submissions for the qualitative component at Emory and UCSB - Contribute to drafting the policy brief targeted at humanitarian stakeholders, Iraqi ministries, and donor agencies - Help prepare conference presentations and materials for an in-country stakeholder workshop MINIMUM QUALIFICATIONS: - A bachelor's degree in a social sciences. - Or a current a student, you must possess a BA/BS or equivalent and be enrolled in a US-based PhD program in social sciences. NOTE: Tasks related to this position can be performed remotely with only occasional visits to an Emory University location. This position requires you to reside in the State of Georgia Additional Details Emory is an equal opportunity employer, and qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by state or federal law. Emory University does not discriminate in admissions, educational programs, or employment, including recruitment, hiring, promotions, transfers, discipline, terminations, wage and salary administration, benefits, and training. Students, faculty, and staff are assured of participation in university programs and in the use of facilities without such discrimination. Emory University complies with Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veteran's Readjustment Assistance Act, and applicable executive orders, federal and state regulations regarding nondiscrimination, equal opportunity, and affirmative action (for protected veterans and individuals with disabilities). Inquiries regarding this policy should be directed to the Emory University Department of Equity and Civil Rights Compliance, 201 Dowman Drive, Administration Building, Atlanta, GA 30322. Telephone: 404-727-9867 (V) | 404-712-2049 (TDD). Emory University is committed to ensuring equal access and providing reasonable accommodations to qualified individuals with disabilities upon request. To request this document in an alternate format or to seek a reasonable accommodation, please contact the Department of Accessibility Services at accessibility@emory.edu or call 404-727-9877 (Voice) | 404-712-2049 (TDD). We kindly ask that requests be made at least seven business days in advance to allow adequate time for coordination.

Rho, an award-winning, stable, full-service CRO known for its collaborative, dynamic culture based in the US, is quickly expanding their presence in Europe. We are a thriving company, and we will deliver global full-service clinical development services and unmatched customer support – worldwide. Join us in redefining what it means to work for a CRO. Working at Rho, you’ll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity’s biggest challenges. At Rho, we believe in the power of passionate individuals working together to make a difference in clinical research. As a Sr. CRA, you will be a key player in our innovative team, dedicated to ensuring that our clinical trials are conducted with the utmost integrity and quality. Your expertise will help us navigate the complexities of clinical research as we strive to deliver meaningful solutions to healthcare challenges. The Clinical Monitoring team at Rho is known for its collaborative spirit and commitment to excellence. Join us to not only advance your career but also contribute to a culture that celebrates innovation, supports professional growth, and values every team member's input. This is a permanent Senior CRA role to be home based role in Poland. Responsibilities: - May contribute to the development of study tools and materials as well as documentation for clinical trials - May provide mentoring, training, and co-monitoring of junior CRAs and other clinical team members - May provide support to the RFP process - Prepare and perform all onsite & off-site/remote site monitoring visit activities across multiple protocols, inclusive of all study visit types as needed (SQV, SIV, IMV and COV), according to Good Clinical Practice (GCP), Protocol, applicable regulations and Sponsor requirements under supervision of experienced staff - Effectively documents observations in site visit reports and follow up letters within timelines required by Rho’s procedural documents and the applicable clinical monitoring plan - Prepare (if needed) and maintain Investigator Site Files (ISF), and maintain site binders and documents of the TMF (Trial Master - May assist in payment processes, including liaison with Site and review Site and patient data for visits being invoiced - Assist in the appropriate identification and action of AE (Adverse Event), SAEs (Serious Adverse Event) and pregnancy reporting procedure - Verify and confirm appropriate IMP (Investigational Medicinal Product) handling at Site and perform drug accountability - Help to plan and perform Country and Site Feasibility, including assessment of potential Risks and challenges, as well as select Study sites and perform pre-study visits - Assist in selection of Study specific Vendors and perform Vendor assessments - Support in negotiation and execution of Investigator/ Institution contracts - May help to prepare documents submission to Ethics Committee, Competent Authorities and other bodies (as applicable), including communication with Sponsor, EC/ CA and other involved parties For Senior CRAs: - Provide mentoring, training, and co-monitoring of junior CRAs and other clinical team members. - May support Clinical Team Lead and Project Management tasks on assigned studies as-requested (e.g. study specific process development, trip report review, newsletter creation, leading CRA project team calls, etc.) - May conduct sign-off visits to assess competency of other CRAs - May attend and present at meetings and conferences, including Investigator Meetings - May participate in the interview and selection process for CRAs

Join us in redefining what it means to work for a CRO. When you work at Rho, it’s more than just a job—you become part of the Rho Factor. We’re a proud bunch of science nerds who love tackling big challenges together. We’re not your typical CRO, and we’re not trying to be. Here, curiosity is encouraged, fresh approaches are welcome, and collaboration is at the heart of everything we do. Whether you’re a data wizard, analytical genius, project mastermind, or any other role, you’ll fit right into the equation of the Rho Factor. Expect plenty of geeky jokes, eccentric personalities, spontaneous brainstorms, and a supportive community where people genuinely care about their work—and each other. You’ll have the opportunity to experience a thriving company with real stability - financial, workforce, and corporate, which has created a safe environment to innovate and develop over a long and rewarding career. We are currently hiring an In-House Clinical Research Associate to join our team! As an In-House CRA here at Rho, you’ll have the opportunity to gain the necessary experience to grow into a traveling Clinical Research Associate (CRA) and work with the Project Manager, traveling CRAs and Lead CRA on a clinical trial to ensure that monitoring activities are properly supported and that critical documents are being tracked, collected, and reviewed. You’ll manage data entered into the CTMS (clinical trials management system) and other project tracking tools. You’ll also assist CRAs on query resolution and data reviews to ensure that studies operate in compliance with study protocols, Rho SOPs, ICH/GCP guidelines, and federal regulations. You may also have the opportunity to mentor other team members. Our Clinical Operations Team will tell you, joining Rho has been one of their best career moves in terms of contentment, financial rewards and career growth, which is why we have such stability in the group! What you'll be doing: - Collect, track and review investigational site records relating to subject screening and enrollment - Assist in the development of study plans and status reports - Collect, track, and review all site regulatory documents - Assist with development and review of Informed Consent Forms - Interact with sites, clients, vendors and internal study team members - Maintain the clinical trials management system (CTMS) and other project tracking tools - Track study supplies and coordinate shipments of supplies to sites as needed - Manage the study Trial Master File (TMF) and ensure periodic TMF audits - Coordinate work with CRAs monitoring on-site - Perform on site co-monitoring and remote monitoring activities - Perform regular reviews of data entered by investigational site staff according to data review/monitoring guidelines