• Відповідати за маркетингові воронки для performance-marketing та SEO • Генерувати та пріоритизувати гіпотези для покращення основних метрик; • Вести експерименти від початку до кінця: планування, запуск, аналіз, ітерація через A/B тести • Будувати персоналізовані воронки під різні аудиторії та джерела трафіку • Працювати в тісній зв'язці з дизайном, розробкою, аналітикою та продуктом; • Керувати очікуваннями користувачів на шляху до реєстрації та будувати міст між маркетингом і продуктом.

• Comply with the Safety Team Roles and Responsibilities • Perform medical review and interpretation of adverse events and device deficiencies reported by clinical trial investigators • Ensure timely and accurate assessment of safety data in compliance with regulatory requirements, study protocols, and internal SOPs. • Write and review adverse event narratives, ensuring clinical accuracy and consistency. Determine relevant follow-up information and ensure completeness of adverse event documentation. • Utilize MedDRA for medical coding and ensure consistency with MedDRA Points to Consider. • Act as a Medical expert for coordination of CEC and DSMB activities and oversee preparation of materials for CEC, DSMB and/or other Committee reviews • Review clinical study data, adverse event reporting, and clinical study design, to safeguard the rights, safety and wellbeing of all trial subjects • Assess safety events, conforming to regulatory requirements and protocol-specific definitions. • Provide medical input into the design of clinical study protocols, including safety endpoints, inclusion/exclusion criteria, and risk mitigation strategies. • Oversee development of study-specific safety documents such as Safety Plan and CEC/DMC charter. • Review and contribute to clinical evaluation reports, clinical study reports, other aggregate safety reports, and regulatory submissions. • Advise on protocol amendments based on emerging safety data or regulatory feedback. • Attend project meetings • Attend and participate in internal meetings as scheduled. • Perform continual assessment of adherence to timelines for all groups involved. • Serve as in-house Medical Subject Matter Expert for NAMSA projects. • For assigned projects, maintain relationship with appropriate C-level / VP-level team member from sponsor side (this is separate from project management discussions which will be the responsibility of the NAMSA Project Manager). • Support business development by contributing to proposals, attending sales meetings, and presenting medical capabilities to prospective clients • Participate in client meetings, including kick-off and safety review meetings, and provide expert input on safety-related matters. • Serve as a clinical and scientific advisor to clients, offering strategic guidance on safety, regulatory, and clinical development issues. • Collaborate with biostatistics, regulatory, medical writing, and clinical operations teams to ensure alignment on safety deliverables. • Participate in the design, testing, and maintenance of electronic systems supporting safety services. • Mentor and coach safety associates and non-medical team members. • Develop and deliver training sessions on therapeutic areas, safety processes, and protocol-specific topics. • Support onboarding new hires and contribute to departmental knowledge-sharing initiatives. • Participate in internal and external audits, inspections, and quality assurance activities. • Ensure compliance with Good Clinical Practice (GCP) and applicable regulatory guidelines. • Maintain and contribute to the development of SOPs, templates, and training materials. • Track and manage safety metrics and key performance indicators. • Support accurate invoicing and budget tracking for safety-related services. • Ensure timely documentation of hours and expenses in accordance with company policy.

Role Description OWT Global seeks a self-driven Tactical Advanced Sensor (TAS) Subject Matter Expert (SME) Level II to support United States Special Operations Command (USSOCOM), Special Operations Forces Acquisition, Technology, and Logistics (SOF AT&L), Program Executive Office for Tactical Information Systems (PEO TIS), and the TAS program portfolio. This role supports the acquisition, test, validation, integration, training, and fielding of advanced sensor capabilities for Special Operations Forces (SOF), including systems associated with unmanned and remote platforms. The TAS SME will translate operational needs into test, evaluation, and acquisition requirements that support rapid, effective fielding to the SOF enterprise. Primary work supports USSOCOM Headquarters and/or OWT Global Headquarters in Tampa, Florida, with remote support as required. Travel may average up to 25%. Qualifications - Five or more years of combined Special Operations and Technical Surveillance Operations/Element/Detachment (TSO/TSE/TSD) experience employing TAS sensors. - Five or more years of Special Operations, Intelligence Community (IC), or similar experience integrating and employing advanced sensor systems, including systems coupled with unmanned capabilities in multi-domain environments. - Ability to translate CONOPs and user needs into acquisition program requirements. - Experience with complex TAS sensor systems, including operational employment, integration, maintenance, testing, troubleshooting, unmanned sensor payloads, and TTL systems. - Ability to work independently in remote and office environments, and outdoors in varied climate conditions as required. - Proficiency with Microsoft Office, including Excel, Word, Visio, and PowerPoint. Requirements - U.S. Citizen - Top Secret clearance while maintaining SCI eligibility - Ability to travel up to 25% of the time - Ability to lift and handle up to 40# - Experience with Tagging, Tracking, and Locating sensors & systems Benefits - Competitive compensation - Comprehensive benefits (medical, dental, vision) - 401(k) with generous company match and immediate vesting - Paid Time Off (PTO) and Federal holidays - Opportunity to support meaningful missions impacting national security

• Coordinate and execute system conversion activities with precision, ensuring data integrity and alignment with project timelines • Analyze and map data between source systems and target platforms, identifying discrepancies and resolving issues proactively • Perform data validation, reconciliation, and quality assurance testing throughout all conversion phases (pre-conversion, conversion, post-conversion) • Troubleshoot and resolve conversion-related issues; escalate complex problems when appropriate • Document conversion processes, mappings, reconciliation results, and testing outcomes for compliance and future reference • Provide post-conversion support to internal teams and clients to ensure a smooth operational transition • Collaborate with partners to define conversion requirements, establish milestones, monitor progress, and validate results • Manage configurations within the Fiserv Optis Platform, Decision Quest (DQ) logic, and Rewards structures • Maintain a deep understanding of system functionality, data structures, and integration points across the Fiserv ecosystem • Manage inserts and messaging by building and testing requirements through Fiserv PCF, PCS, and DQ • Own the setup, testing, and ongoing maintenance of settings within PCF • Own the setup and ongoing maintenance of decision logic criteria within DQ • Manage the setup and testing of Rewards structures using Fiserv DMM tables and Rule logic • Identify opportunities to streamline conversion processes, optimize workflows, enhance automation, and improve integration efficiency • Ensure all work adheres to company policies, regulatory standards, and financial industry best practices • Lead Fiserv-related projects by coordinating testing, validation, and implementation with internal stakeholders • Support configuration updates, integration enhancements, and cross-functional operational initiatives • Perform other duties as assigned