• Develop and secure business within the life science space focusing on strategic pricing and contracting • Manage a portfolio of clients to meet client needs with a $500K annual sales target • Conceptualize project scope for clients, assemble teams, and oversee them from initiation to delivery • Serve as a subject matter expert on government pricing and reporting • Create strategic and tactical recommendations for optimal market access • Solve complex client issues in a timely manner with minimal management oversight • Generate public recognition for Avalere’s pricing capabilities through publications and speaking engagements • Mentor, supervise, and train staff within the Market Access practice

• Supports the Global Clinical Study Manager in global study delivery and ensures that delegated components of clinical studies are executed to expected and specified quality standards, within timelines and budget • Supports the alignment of study goals with clinical operations goals and objectives under direction of the Global Clinical Study Manager • Supports study vendor management in addition to other study management activities assigned • Supports the Global Clinical Study Manager with the organization and logistics for cross-functional Clinical Study Team (CST) meetings • Establishes good collaboration with the Global Clinical Study Manager, Regional Clinical Trial Management Associates and other key stakeholders globally and regionally • Knowledgeable of clinical study operations, including interpretation and implementation of regulatory and ICH-GCP guidelines • Builds solid knowledge of global clinical trials operations under the guidance of the Global Clinical Study Manager • Actively contributes to GSMA task force initiatives and cross functional projects within scope, supporting process improvement, standardization, and implementation activities as required • Creates and maintains study-level SharePoint and CST distribution lists • Sets up the study in the appropriate systems e.g. eTMF, CTMS etc and makes sure study-level information is kept up to date • Ensures system access is granted and managed appropriately across the study life cycle, supports user account management for systems used in study • Supports the development of various study plans • May assist in the review of study-related documents as delegated by the Global Clinical Study Manager (e.g., Clinical protocols, Informed consent forms, Investigator Brochures, Pharmacy Manual, Monitoring Plan, Laboratory Manual, Patient Diary, Pharmacy Manual, Case Report Form (CRFs), CRF Completion Guidelines and other relevant study plans and charters) • Organizes study-specific investigator meetings under supervision of the Global Clinical Study Manager • Might support the creation and review of site feasibility assessments required for study participation • Manages and tracks key study deliverables such as screening, enrollment, biological samples and images, data flow and protocol deviations in relevant systems in collaboration with Regional Clinical Trial Management Associates • Prepares metrics and updates to key deliverables for management as per information available in relevant systems • Supports the preparation of a study newsletter and other correspondence related to the study conduct (e.g. frequently asked questions, lessons learned) in collaboration with the study team • Supports the TMF specialist with study-level TMF creation and, as required, maintains the study-level TMF, including regular review and QC of TMF documents as per the study TMF QC plan • Supports the Global Clinical Study Manager with study drug forecasts and overall study drug supply activities in collaboration with Global Clinical Supplies • Supports the overall data cleaning activities and contributes to the follow-up of outstanding information • Supports the Global Clinical Study Manager with planning and execution of the Clinical Study Report • Supports the identification of operational risks and issues and works with the Global Clinical Study Manager to recommend solutions for discussion with appropriate team leadership • Learns and shares best practices in clinical operations methodologies, systems and processes with an emphasis on quality and compliance • Suggest improvements to enhance efficiency and the quality of the work performed on assigned projects • Might support the development of global study tools, working instructions and SOPs • Supports selection and set-up of vendors for global outsourced activities • Supports study budget management activities with responsibility for PO setup and payment invoice tracking across all study lifecycles.

• Evaluates and maintains existing policy information to ensure data is current, accurate, and appropriately priced for renewal • Responds to client requests and questions, offering information and advice regarding the insurance products & underwriting appetite • Communicates with clients to gather necessary information, resolves inquiries, and ensures a smooth underwriting process • Prepares and organizes documentation related to underwriting submissions and policy issuance • Assesses risks associated with individual insurance applications, considering both standard and substandard criteria • Provides support in premium calculations, ensuring accurate application of rates based on underwriting guidelines • Builds and maintains reports on underwriting activities, key performance indicators, and relevant metrics • Conducts internal and external audits by providing necessary documentation and information related to underwriting activities • Ensures adherence to company policies, guidelines, industry regulations, and compliance standards in underwriting activities • Collaborates with underwriting teams to relay information, coordinate tasks, and contribute to the overall underwriting process • Serves as the key point of contact for customers and agents and delivers excellent customer service by addressing inquiries, resolving issues, and ensuring a positive experience for them

• Support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by either the agreed algorithm or the Sponsor’s requirements, including pre-award activities. • Develop simple investigator grant estimates and proposal text to support the proposal development process. • Utilize and maintain contract and budget templates and contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the Scope of Work and Project Plan, within the agreed project strategy. • Ensure collaboration, including communication with sponsors, stakeholders and RSU regions and countries, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan. • Provide specialist operational and financial contracting support to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. • Assist in the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required. • Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and the wider company, as required. • Ensure overall contracting efficiency and adherence to project timelines and financial goals; report contracting performance metrics and out of scope contracting activities as required.