• Lead enterprise implementation projects involving multiple workstreams, geographies, and third-party partners. • Develop, present, and maintain detailed enterprise-level program plans, roadmaps, financials, and executive dashboards. • Facilitate executive steering committees, ensuring transparent communication of status, risks, issues, and financial performance. • Anticipate and manage interdependencies across technical, operational, and business teams to ensure project success. • Negotiate and manage scope changes with executive sponsors, ensuring proper documentation, financial impact analysis, and change order processing. • Ensure strict compliance with regulatory, contractual, and industry requirements in delivery. • Codify lessons learned and contribute to the PMO’s strategic evolution. • Act as a trusted advisor to clients and represent Mission Cloud/CDW in strategic forums.

• Govern project budgets, timelines, risks, assumptions, scope changes, issues and dependencies; report out to clients and team members • Plan, schedule, document and manage activities throughout cloud consulting engagements as a billable project manager • Lead consulting sessions with Delivery team to understand challenges, technical needs, and customer requirements • Document and present recommendations to customers, including senior leadership • Manage comprehensive project plans and validate requested deliverables, resource requirements, internal goals, client priorities and milestones • Control and analyze project finances by ensuring project funding is secured and documented and creating cost estimates that are aligned with resource requirements • Coordinate relationships with customers and vendors to identify problems, create solutions, and implement efficiency improvements • Manage scope changes and customer expectations through the change order process • Work with Mission Cloud service delivery leadership and sales resources to scope work efforts for project services

• Own all aspects for project management of US and global quantitive healthcare market research project from award through final invoicing so that projects are delivered on time, within budget, and meet client expectations • Manage multiple partners at once to support the successful delivery of projects - including developing and executing strategies to proactively address challenges with fieldwork • Work closely with team members across MedSurvey to further strengthen and deep client relationships by identifying and addressing challenges, providing feedback on projects, documenting lessons learned, and providing input into proposals for the successful delivery of future projects

• Responsible for management/oversight of study country level activities from study startup through conduct and study close • May manage the study start up process in countries assigned (where SUPM not assigned) and/or oversee CRO responsible for these activities as applicable • Through the Site Care Partner/Country Trial Manager or pCRO supports the Country/investigator outreach process, site identification and feasibility ensuring countries/sites can meet all study protocol requirements • Provides country level input on Startup and Recruitment milestones as provided by pCRO and/or Country Trial Manager/Site Care Partner to Global Study Manager during planning • Is accountable for overseeing pCRO and/or Country Trial Manager/Site Care Partner for assigned studies at country level in accordance with the overall project plan, manages and maintains accurate country level plans (e.g. timelines, budget, risk and quality plans) • Collaborates with accountable roles to identify and manage deviations and risks in study startup and execution and implements mitigation strategies as required. • Is also accountable for resolution of Site Activation escalations to Study Teams including offering options for mitigation • Leader of the Local Study Team (core members: (Lead) Site Care Partners, Clinical Trial Associate, ad hoc members: ICL, Site Activation Partner, CTRO and Local Regulatory, Medical Affairs colleagues and other key stakeholders as required) • Ensures compliance to relevant Global and Local, internal and external requirements and regulations • Ensures timely communication bidirectionally between the global and local study team. • Provides protocol level guidance and support to responsible Local Study Team members as applicable. • Liaise with Site Care Partner, Lead Site Care Partner, Site Activation Partners and Regulatory colleagues in country to agree on submission strategy to Health Authorities and Ethic Committees • Utilizes roles in country such as Lead Site Care Partner, and expert roles such as Contracts Leads, Site Activation Partners to provide the Global Teams with local intelligence and operational nuances to be considered • Acts as the study level point of contact for all study-level questions for the Local Study Team, ensuring resolution at lowest possible level, and when needed liaising with and escalating to appropriate global roles/teams • Follows up on region/country level issue status to ensure resolution. Identifies country level trends to improve deliverables processes as needed • Utilizes country intelligence to provide input on country specific risks into preparation of Investigational Quality Management Plan, Study Monitoring Plans, ensures PTMF completeness and oversight of all relevant compliance activities for allocated studies • Ensures audit/Inspection readiness during start-up and conduct • Manages applicable Quality Events with pCRO and local team as applicable and required • Coordinates effective site recruitment planning to allow for implementation of plans at the country and site level, consistent with global plan and local targets • Responsible to drive and ensure delivery of data cleaning deliverables for pCRO and sites as applicable • Provides input on Country level Per Subject Costs, local vendor costs and other fees where applicable • Responsible for PTA and SIV report review for reports completed by the Site Care Partner • Provides country level documents to PTMF and maintains oversight of Investigator Site File (ISF) reconciliation and completeness actions • Ensures pCRO and/or applicable internal study team members maintain appropriate level IP/equipment/ancillary supplies management including Import/Export License management with the support of Clinical Trial Associates and other roles as required • Supports implementation of new tools and technologies (e.g. eConsent, eISF, Remote Source Access, remote SDV/SDR, iConnect, implementation of protocol required decentralized trial options etc.) • Support Identification, contract development and management of local vendors or facilities as per protocol • Investigator Meeting support and management including doing presentations as appropriate • Management of local Investigator Meetings including doing presentations as appropriate