• Contributes to the selection of potential investigators • In some countries, as required, CRAs are accountable for study start-up and regulatory maintenance • Tasks may include Site Qualification Visits, collection, preparation, review and tracking of documents for the application process; submission of proper application/documents to EC/IRB and to Regulatory Authorities for start-up and for the duration of the study • Trains, supports and advises Investigators and site staff in study-related matters, including Risk Based Quality Management (RbQM) principles • Confirms that site staff have completed and documented the required trainings appropriately, including ICH-GCP training, prior to and for the duration of the study • Ensures the sites are inspection ready at all times • Actively participates in Local Study Team (LST) meetings • Contributes to National Investigators meetings, as applicable • Initiates, monitors and closes study sites in compliance with AZ Procedural Documents • Shares information on patient recruitment and study site progress (site quality/performance) within the LST • Drives performance at the sites • Proactively identifies and ensures timely resolution to study-related issues and escalates them as appropriate • Updates CTMS and other systems with data from study sites as per required timelines • Manages study supplies (ISF, etc), drug supplies and drug accountability at study site • Prepares study drug for destruction, if applicable • Performs monitoring visits (remote and onsite), as well as remote data checks, in accordance with the timelines specified in the study-specific Monitoring Plan • If required, determines and discusses with LSAD the correct timing and type of visits • Performs Source Data Review (SDR), Case Report Form (CRF) review and Source Data Verification (SDV), in accordance with the Monitoring Plan • Performs regular Site Quality Risk Assessments and adapts monitoring intensity accordingly during the study • Ensures data query resolution in a timely manner • Works with data management to ensure robust quality of the collected study data • Ensures accurate and timely reporting of Serious Adverse Events and their follow-ups • Prepares and finalises monitoring visit reports in CTMS and provides timely feedback to the Principal Investigator, including follow-up letter, within required timelines and in line with AZ SOP • Follows up on outstanding actions with study sites to ensure resolution in a timely manner • Follows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, CSP or ICH-GCP compliance issues to Local Management and/or CQM as required • Assists site in maintaining inspection-ready ISF • Prepares for and collaborates with activities associated with audits and regulatory inspections in liaison with LSAD and CQAD • Ensures timely collection/uploading of essential documents into the eTMF in accordance with ICH-GCP, AZ SOPs and local requirements • Supports/participates in regular QC checks performed by LSAD or delegate • Ensures that all study documents under their responsibility (i.e., site documents, relevant communications, etc.) are available and ready for final archiving and completion of local part of the eTMF • Provides feedback on any research-related information including sites/investigators/competing studies that might be useful for the local market • Ensures compliance with AstraZeneca’s Code of Ethics, company policies and procedures relating to people, finance, technology, security and SHE (Safety, Health and Environment) • Ensures compliance with local, national and regional legislation, as applicable • Collaborates with local MSLs as directed by LSAD or line manager

• Assist in the management of the laboratory • Work directly with Dr. Koss to make major contributions to ongoing research projects • Assist with in-vivo experiments • Perform flow-cytometry, western blot, PCR, and cell culture techniques • Maintain supplies for adequate laboratory function and order supplies and equipment as needed • Maintain laboratory safety manuals and equipment • Demonstrate a willingness to learn new concepts and technical skills • Harbor an enthusiasm for working in a team-based environment

Role Description The Research Officer will play a central role in driving the research, analysis, and practical tool development underpinning GSG Impact’s Domestic Capital Mobilisation (DCM) work. The role combines strategic research, market analysis, stakeholder engagement, and practical framework development across multiple emerging market contexts. The successful candidate will work closely with GSG Impact’s Knowledge & Impact Practice and Regional Coordination teams, as well as external stakeholders including investors, policymakers, regulators, DFIs, fund managers, and ecosystem actors. The role will primarily support: - Phase 1: DCM solution sprint and pilot set-up (June–September 2026) - Phase 2: DCM Playbook co-creation (October 2026–June 2027) Key Responsibilities - Phase 1: Research, analysis, and pilot preparation - Lead primary and secondary research on domestic capital mobilisation in emerging markets. - Conduct market analysis and segmentation of domestic capital pools, including pension funds, insurance companies, development banks, sovereign funds, and other institutional investors. - Analyse investor mandates, risk-return expectations, regulatory constraints, and catalytic capital needs. - Review and synthesise global and country-level examples of domestic capital mobilisation, impact investment vehicles, and catalytic capital structures. - Conduct stakeholder mapping across investors, policymakers, regulators, ecosystem actors, DFIs, and fund managers. - Support interviews and consultations with National Partners and external stakeholders. - Develop analytical frameworks and practical tools, including a country readiness / feasibility assessment framework for domestic capital mobilisation. - Contribute to the development of the DCM Field Insights Compendium and related knowledge products. - Support country selection and assessment processes for deeper engagement and pilot work. - Phase 2: Playbook co-creation and country engagement - Support the development and iteration of the Domestic Capital Mobilisation Playbook and related tools and templates. - Contribute to practical guidance on capital pool analysis, stakeholder engagement, policy levers, market coordination, and investment vehicle pathways. - Support workshop preparation, facilitation materials, stakeholder sessions, and knowledge-sharing activities. - Capture and synthesise lessons learned from country implementation and Partnership engagement. - Support validation and refinement of Playbook content with National Partners, investors, ecosystem actors, and external experts. Qualifications - Strong analytical and structured problem-solving skills, ideally developed through consulting, research, advisory, or strategy roles. - Experience conducting both primary and secondary research, including interviews, market analysis, and synthesis of complex information. - Strong writing and communication skills, with the ability to translate complex analysis into practical and actionable outputs. - Experience developing practical tools, frameworks, templates, or market intelligence products. - Strong stakeholder engagement and facilitation capabilities, including experience working across multiple stakeholder groups. - Experience in impact investing, blended finance, domestic capital mobilisation, SME finance, or financial sector development, particularly in emerging markets. - Understanding of institutional investors, investment vehicles, catalytic capital structures, and policy or regulatory environments related to capital markets. - Ability to manage multiple workstreams and work independently in a fast-moving, entrepreneurial environment. - Experience working across emerging markets and with ecosystem-building organisations, DFIs, donors, or policy stakeholders is strongly preferred. - Minimum of 4 years of relevant experience in similar roles is strongly preferred. Requirements - Closing date for applications: 25th May 2026 11.59pm BST - This is a 12 month FTC with a maximum of 100 working days. Day rate to be negotiated.

• Drafts project deliverables, interacts with clients, and contributes to strategic thinking under the direction of senior staff • Supports scientific coordination and project management • Develops scientific deliverables (e.g., protocols, reports) under oversight of senior staff • Participates in scientific guidance/consultation on project design and conduct • Leads on or oversees development of project deliverables for senior review • Interacts directly with project sponsors, physician experts, and clinical sites • Assists in monitoring project budget spend and managing timelines for scientific tasks/deliverables • Participates in development of abstracts and manuscripts • Contributes to business development activities, including support of proposal development