• Contribute to study management, ensuring that individual project targets are met and services are provided according to the highest quality standards, policies and procedures. Escalate project risks appropriately. • Plan and communicate to team members study specific tasks and project priorities. • Analyze and interpret various financial reports and monitor project finances. • Train study teams on site payment process, including setting expectations around site payments' requirements and deliverables. • Generate reports for study-level KPIs and metrics; evaluate and interpret data. Escalate performance issues to management. • Attend internal team meetings and provide updates on payment statuses. • Manage escalations (project team, site and sponsor) regarding payment issues. • May generate payments in accordance with procedural documents and site contracts. May build and enter budgets and SVTs; work on transparency reporting; perform study reconciliations; manage and maintain investigator funds tracker for studies transitioned to site payments. • May review and approve payments, budgets, and/or reconciliations, etc., in accordance with procedural documents and site contracts.

• Manage, coordinate and evaluate medical projects for one or more programs in collaboration with management and other stakeholders. • Work independently to perform first pass review of safety data, utilizing line listings, company dashboard(s) and/or other visualization tools. • Review safety data and provide summations for safety review meetings. • Independently function as the Project Lead for medical monitoring services when SAE case processing has not been contracted. • Create and maintain medical management plan(s) on studies. • Work independently to monitor the project financial status, unit forecasting, actual realization, and team allocations in systems. • Resolving complex problems through in-depth evaluation of various factors and offers solutions. • Present at business development, client, and investigator meetings and participates in strategy/business development calls.

• Coordinate and review safety data, utilizing line listings, company dashboards and/or other visualization tools • Review data for safety trends, coding consistencies, and potential follow up with investigator sites • Identify potential issues and resolve or escalate as appropriate • Review safety data and may provide summations for safety review meetings • May review designated sections of aggregate reports • May help to create/review safety and medical management plan(s) on studies and ensures that the processes included in plan documents are reflective of the contract and services requested • May help manage routine project implementation, forecasting and coordination, including review of metrics and budget considerations • Monitor the status of the data review and escalate any delays and/or risks to all stakeholders, including study leads • May present at business development, client, and investigator meetings and participate in strategy/business development calls • Resolve complex problems through in-depth evaluation of various factors and offers solutions • May serve as the primary point of contact for clinical/data management project teams • May assist management in training and mentoring

• Work independently to perform and/or lead first pass review of safety data utilizing line listings, company dashboard(s), and/or other visualization tools. • Review data for safety trends, coding consistencies, and potential follow up with investigator sites. • Proactively identify any potential issues and resolve or escalate as appropriate. • Review safety data and provide comprehensive summations for safety review meetings. • Initiate and lead initiatives to improve current processes and develops new processes regarding medical monitoring and department services. • Independently function as the Project Lead for medical monitoring services when SAE case processing has not been contracted. • Manage project implementation, coordination, maintenance and close out of assigned studies as applicable. • Serve as the primary point of contact for clinical project teams on studies and can act as the alliance level lead on larger alliance/multi-protocol studies. • Create and maintain safety and medical management plan(s) on studies (as applicable) and ensure that the processes included in the plan document are reflective of the contract and service requested for studies that have department involvement as well as standalone studies (ex. MM and/or MPC). • Work independently to monitor the project financial status, unit forecasting, actual realization, and team allocations in systems. • Coordinate staff projections based on contract values and actual hours used. • Escalate any financial and/or operational risks and can attend risk management meetings to discuss. • Present at business development, client, and investigator meetings and participate in strategy/business development calls. • Represent studies at risk management meetings. • Independently determine hours required for out of scope work for both the MM and MPC and provides this to the finance/study team for contract modifications. • Attend meetings to discuss/justify the modification requirements. • Train and develop new team members. • Serve as main point of contact for team member questions with escalation to management as appropriate. • May provide input on individual performance to direct line manager. • Organize and lead meetings with team members to discuss potential process issues, answer questions, and brainstorm ideas and solutions. • Resolve complex problems through in-depth evaluation of various factors and offers solutions.