Role Description Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiological Practices (GPP) and protocol compliance. - Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team and with guidance develops action plans. - Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes. - Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate. - Demonstrates diligence in protecting the confidentiality of each subject/patient. - Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. - For the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes. - Conducts Source Document Review of appropriate site source documents and medical records. - Verifies required clinical data entered in the case report form (CRF) is accurate and complete. - Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines. - Utilizes available hardware and software to support the effective conduct of the clinical project data review and capture. - Verifies site compliance with electronic data capture requirements. - May perform investigational product (IP) inventory, reconciliation and reviews storage and security. - Verifies the IP has been dispensed and administered to subjects/patients according to the protocol. - Verifies issues or risks associated with blinded or randomized information related to IP. - Applies knowledge of GCP/local regulations and organizational procedures to ensure IP is appropriately (re)labelled, imported and released/returned. - Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. - Reconciles contents of the ISF with the Trial Master File (TMF). - Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations. - Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan. - Supports subject/patient recruitment, retention and awareness strategies. - Enters data into tracking systems as required to track all observations, ongoing status and assigned action items to resolution. - For assigned activities, understands project scope, budgets, and timelines; manages site-level activities/communication to ensure project objectives, deliverables and timelines are met. - Must be able to quickly adapt, with the oversight of the Lead CRA, to changing priorities to achieve goals/targets. - May act as primary liaison with project site personnel, or in collaboration with another CRA or Central Monitoring Associate (CMA). - Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements. - Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. - Participates in global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project specific requirements. - Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions. - For Real World Late Phase, the CRA I will use the business card title of Site Management Associate I. - Additional responsibilities include: - Site support throughout the study lifecycle from site identification through close-out. - Knowledge of local requirements for real world late phase study designs. - Chart Abstraction activities and data collection. - Collaboration with Sponsor affiliates, medical science liaisons and local country staff. Qualifications - Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience. - Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements. - Must demonstrate good computer skills and be able to embrace new technologies. - Excellent communication, presentation and interpersonal skills. - Ability to manage required travel of up to 75% on a regular basis. Additional Information - As part of your employment with Syneos Health, you may be deployed to Sites that require certain medical and other personal information to gain facility access. - Pursuant to our Employee Privacy Notice, Syneos Health can provide the Sites with the information necessary for you to gain such access. - Further, a Site may ask you for additional information beyond that which Syneos Health has in its possession. - You are required to comply with any such Site requests as a condition of your employment with Syneos Health. - Please note that failure to provide requested information may result in a Site barring you from entry, which could put your ongoing employment at risk.

• Manage all onboarding activities including project kick-off, training, configuration, data migration, and launch to help clients reach value quickly. • Oversee several implementation projects at once, keeping them on schedule and aligned with customer goals and satisfaction. • Work closely with venue stakeholders to understand their goals and customize the SevenRooms platform to meet their needs. • Guide clients through the platform, helping them learn and apply tools based on their unique business objectives. • Partner with Sales and Customer Success to support a smooth handoff and drive product adoption.

• Building and maintaining strong relationships with key stakeholders at clinical trial sites, including principal investigators, site coordinators, and research staff. • Providing support and guidance to site staff on study protocols, procedures, and regulatory requirements, ensuring compliance and successful study conduct. • Identifying opportunities to improve site engagement and optimize site performance through regular communication and feedback mechanisms. • Collaborating with internal teams to develop and implement site engagement strategies tailored to the specific needs of each study and site. • Monitoring site performance metrics and providing regular updates to study teams on site engagement activities and outcomes.

Role Description We’re searching for an Affiliate Revenue Manager to drive the full-cycle of affiliate management from understanding the client’s need and revenue requirements to content production and performance improvement. In this role, you’ll have the opportunity to secure industry-leading deals, unlock new revenue streams across global markets, and turn traffic into scalable business results. - Drive affiliate revenue by securing high-value CPA, RevShare, and hybrid partnerships with exchanges, brokers, and crypto platforms, negotiating exclusive above-market terms, and developing geo-specific monetization strategies across 26 markets to maximize revenue per region. - Based on the developed monetization strategy, produce high-quality evergreen, affiliate content (product reviews, comparisons, how-to guides, tutorials, listicles, case studies) aligned with editorial standards. - Audit, optimize, and improve affiliate placements, funnels, and conversion paths to boost CTR and performance. - Analyze EPC (earn-per-click), conversion rates, and traffic performance to continuously improve monetization. - Collaborate closely with editorial and partnerships teams to ensure a cohesive cross-functional content strategy. - Manage AdButler infrastructure, including placements, naming conventions, campaign setup, and creation of HTML/animated banners, while running A/B tests to optimize formats and targeting. Qualifications - Have at least 3 years of experience in affiliate deal negotiations, content production, and optimization. - Fluent in English; additional languages are a strong advantage. - Have expertise in SEO and driving clicks to the content. - Hands-on experience with WordPress or similar CMS. - Experienced with AI tools (e.g., Claude, other LLMs) in content workflows. - Solid knowledge of crypto, forex, and traditional finance. - Established network with affiliate managers at top exchanges, brokers, or crypto platforms. - Proven experience negotiating CPA, RevShare, and hybrid deals with strong market awareness. - Familiar with affiliate platforms (Impact, Tune/HasOffers, Awin) and attribution models. - Data-driven mindset: able to track EPC, conversion rates, and optimize performance. - Experience with ad servers (e.g., AdButler or similar). Benefits - 100% remote work — no location limits. - Flexible working hours to suit your lifestyle, no time trackers. - Paid time off to recharge. - Clear goals and freedom to define how you achieve them. - Access to major crypto events & conferences. - Internal learning programs & masterclasses. - Culture of open communication and constructive feedback. - Support for personal branding and industry visibility. - Career growth opportunities — most of our managers are promoted internally. - An inclusive workplace where everyone can thrive.