Role Description This position will support project teams in completion of commercial and government clinical research projects. Perform duties under the direction of the clinical research managers and more experienced staff. Create, review, and maintain project documentation according to project requirements. Work with staff to investigate problems and resolve or recommend solutions. Coordinate with clients, sponsors, and site personnel to ensure project needs are met. This will be a 20 hour a week position. Compensation: $28,500 - $30,000 annually, hourly time entry will be required. - Apply basic clinical research methodologies to meet protocol and regulatory requirements. - Assist in the development of client deliverables according to project requirements, including but not limited to, project-specific documentation, operating procedures, and work flows with direction of more experienced staff. - Process incoming and outgoing project materials to monitor, verify, and track receipt of documentation and ensure appropriate distribution of materials to internal and external research personnel and sites. - Interact with clinical site staff regarding study activities, questions and problems. - Perform general quality checks of documentation. - Prepare general correspondence, agendas and meeting minutes, reports, and other project-specific documentation. Ensure review, approval, and distribution to internal staff and external project participants. - Provide logistical support for committee meetings and DSMB meetings, including planning, arrangements, travel and post-meeting activities and writing reports. - Update spreadsheets and other tracking tools to reflect project status. - Identify and investigate problems and with more experienced staff on corrective actions. - Report status of activities and problems to senior team members as appropriate. - On occasion, assist with data management activities. - Maintain clinical research files and related documents. - Ensure tasks are completed on time and work is of the highest quality. - Perform related duties as assigned. Qualifications - Bachelor's Degree in science, health, or related field. - Knowledge of Microsoft Office tools such as Word, Excel, and PowerPoint. - Must be comfortable working in fast-paced environment and managing a heavy workload and multiple projects with competing priorities, with ability to switch priorities quickly as needs change. - Exceptional interpersonal skills and written and verbal communication skills. - Good decision-making abilities and problem-solving skills. - Strong organizational skills; accurate and detail-oriented. Benefits - Competitive salary. - Medical benefits. - PTO. - Holiday pay. - More. Company Description MPF Federal is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

• Conduct market research across a range of sectors, companies, and business topics • Gather, verify, and organise information from multiple sources • Prepare summaries, briefs, and research outputs for internal use • Analyse findings and present them in a clear and structured format • Track developments, trends, and relevant market activity as required • Maintain research files, reference materials, and working documents • Support ad hoc research requests with accuracy and good turnaround times • Contribute to continuous improvement by helping refine research processes and documentation

Role Description The Market Research Analyst supports internal research across a range of priorities within Haldren. The role involves gathering, organising, and analysing information, structuring findings clearly, and producing work that is accurate, usable, and relevant to current business needs. This position suits someone who is comfortable working across different research requests, managing deadlines, and maintaining a high standard of quality in day-to-day output. The analyst will work independently in a remote environment, interfacing directly with internal stakeholders and contributing to the quality and reliability of Haldren's research capability. Key Responsibilities - Conduct market research across a range of sectors, companies, and business topics - Gather, verify, and organise information from multiple sources - Prepare summaries, briefs, and research outputs for internal use - Analyse findings and present them in a clear and structured format - Track developments, trends, and relevant market activity as required - Maintain research files, reference materials, and working documents - Support ad hoc research requests with accuracy and good turnaround times - Contribute to continuous improvement by helping refine research processes and documentation Qualifications - Experience in market research, business research, intelligence, or a related analytical role - Strong ability to work with information in a structured and accurate way - Good written English and the ability to present findings clearly - Strong attention to detail and commitment to source accuracy - Ability to manage multiple tasks and changing priorities - Confidence working independently in a remote environment - Good judgement when handling research requests and interpreting findings - Comfortable using online research tools, spreadsheets, and standard office software Requirements - Experience supporting internal business, commercial, or strategy-focused research - Exposure to company research, competitor research, or industry analysis - Strong Excel or Google Sheets capability - Experience preparing slides, summaries, or briefing materials - Familiarity with professional services, recruitment, or consulting environments Benefits - Remote work arrangement - Opportunities for professional growth - Flat management structure with direct access to decision-makers - Open communication environment

• Provides clinical project oversight and support to the project management (PM) team. • Provides oversight and manages clinical monitoring and site management portions of projects in accordance with ICH/GCP, CFR guidelines, regional or country regulations/ legislations, as well as UBC and sponsor SOPs. • Thorough knowledge of sponsor specific project requirements, scope, protocol and timelines. • Provides oversight of the day-to-day clinical operations of US, European and/or multi-national global projects from start-up through close-out. • Reviews and approves monitoring reports and letters within UBC and/or sponsor timelines. • Leads and assists with UBC and project specific training. • Ensures appropriate visit scheduling per protocol; tracks, reports and escalates adherence to site visit schedule, trip report metrics and documentation of completed tasks. • Provides oversight of the issues & actions and protocol deviations to ensure timely resolution per UBC and/or sponsor timelines. • Serves as primary liaison for monitoring issues, escalating to PM and/or Evidence Development Operations (EDO) Manager when appropriate. • Assists with preparation and leading of sponsor, project team and UBC meetings. • Assists as back-up for PM and may be primary contact for UBC/sponsor interaction. • Collaborates with PM to provide input into resourcing, analyzing cost variances, out-of-scope management, and conducting revenue recognition as applicable. • Coordinates site assignments for team in conjunction with PM and EDO Manager. • Monitors clinical operations aspects of the project against the established plans, SOPs and KPIs ensuring compliance. • Assists PM with the creation and maintenance of project specific documents. • Responsible for maintenance of audit-ready project systems (eTMF, CTMS, project specific systems) as related to clinical operations. • Mentors and supports project team. • May include reviewing the preparation, submission and tracking of Competent Authority (CA), Central and Local Ethics Committee and other regulatory applications, as per country requirements. • May include oversight of contract negotiation activities with the sites as per country requirements. • May be required to perform site monitoring as needed. • May review and provide oversight of study feasibility assessments. • May assist PM and EDO Manager with management of Vendor CRAs. • May require up to 30% travel. • Assists with other duties as assigned.