• Monitor and own the progress of clinical studies at investigative sites • Ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. • Coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.)

Role Description IDC is seeking a Research Agenda Coordinator for IDC's business operations team. This position at IDC might be the perfect fit for you. We're building a team of data and research coordinators as a part of an exciting new role at IDC. We are seeking candidates with experience to collect, analyze, and interpret data on our published research to advise research agendas and in turn manage the execution and delivery of the plan. This position will be central to developing insights to help market researchers confidently build a research agenda plan that entices readers to become IDC clients. Responsibilities - Data discovery, identification and data collection around market research - Standardization - research and recommend standardization practices to creating and delivering compelling research - Project planning and organization to inform and advise the analyst's research agenda - Data analysis including quality checks, extracting key findings, suggested quality remediation - Agile collaboration with technology analysts and business operations teams (information exchange, decision making) Qualifications - 5+ years' experience as a Data Analyst, Market Analyst, Business Analyst or Data Scientist - Strong understanding of market research and report publication - Advanced Excel (e.g. pivot, flat file, vlookup, offset, match) - Advanced Power Point creation skills - Communication skills - Explaining issues, findings effectively - Analytical skills - i.e. find and classify the important bits of data - Attention to detail - Eager to find issues - Coachability and willingness to learn new systems and skills - Open feedback mindset (question and candor) - Creative data problem-solving including ability to create synthetic data with low levels of data input - Ability to gain trust, negotiate and work with technical teams and business stakeholders - Project management or program management skills Requirements - Experience with LLM Chat interface search and Web data analysis (e.g. Perplexity, ChatGPT Deep Research) - Previous experience in companies providing market research agendas - Workflow management and project tools (Monday.com) Benefits At IDC, your work helps shape how the world understands technology and where it goes next. You collaborate with curious, high-caliber colleagues who value rigor, integrity, and shared success. As the premier global provider of trusted technology intelligence, IDC equips business and technology leaders with the evidence they need to make confident decisions. Our insights inform strategy, investment, and innovation across industries and regions. Recognized by IIAR as Analyst Firm of the Year for five consecutive years, IDC sets the standard for credibility and impact. With more than 1,000 analysts worldwide and a truly global perspective, we combine deep expertise with practical relevance. Here, your ideas matter, your voice is heard, and your contributions provide the insights leaders rely on every day. It is meaningful work, backed by a culture that supports growth, collaboration, and long-term career development with a globally respected brand. Company Description IDC is committed to providing equal employment opportunities for all qualified persons. Employment eligibility verification required. We participate in E-Verify.

• Responsible for organizing, communicating and evaluating team objectives for clinical studies. • Participates in study design and study preparation activities, as applicable. • Develops and revises clinical trial documentation including clinical trial protocol development, case report form (CRF) development, IRB/Ethics submissions. • Participates or leads the process to evaluate and select potential investigators and sites. • Participates or leads the process to evaluate and select potential vendors as applicable. • Conducts or oversees site visits as required (pre-study, initiation, interim and close-out visits) to ensure protocol compliance, accurate and thorough data collection, and appropriate study conduct. • Develops and revises site training tools, interprets clinical data, manages investigational sites, develops tracking tools and performs other clinical activities as needed during clinical study conduct. • Leads clinical study teams focused on conducting clinical programs consistent with applicable regulations, guidelines, and policies. • Manages project timelines and vendor performance to meet departmental and corporate goals. • Monitors and tracks clinical trial progress and provides status update reports. • Manages study budget, payment process and reconciliation of invoices for all clinical trial vendors including investigative sites when applicable. • Oversees work produced by junior clinical team members. • Manages all clinical trial vendors (e.g., IRB, IVRS, central/core labs, such as angiogram, ultrasound, or central ECG). • Analyzes and evaluates clinical data gathered during research. • Leads, prepares and reviews project and study-related documents including: informed consent forms, investigational brochures, case report forms, monitoring plans, synopses, protocols and amendments, and other appropriate sections for studies conducted under Investigational Device Exemption (IDE) or 510(k) application. • Responsible for authoring internal documents and clinical study reports and assisting with clinical evaluation reports. • Develops and revises annual, interim, and final reports and clinical sections of Pre- or Post-Market Approval submissions. • Coordinates the design, format and content of CRFs, study guides, study reference binders, and forms including participating in the EDC and IVRS specification process and UAT. • Coordinates and manages Investigational Product including overall accountability and reconciliation. • Responsible for selection of CRO study staff and coordinating training including documentation. • Leads the review of clinical data at the CRF, data listing, and report table levels. • Represents Clinical Affairs at the Project Team level for individual studies, as appropriate • Identifies and escalates site, vendor and study related issues to supervisor, as appropriate • Oversees clinical and adverse event data evaluation during the conduct of the study and for completion of clinical study reports. • Working knowledge of CEC and DSMBs. • Manages training of investigators, site staff, and SWMI clinical staff. • Oversees quality by maintaining compliance, reviewing device complaints, reviewing audit reports and implementing corrective and preventative actions. • Other duties as assigned.

• Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan and applicable prevailing laws, Good Clinical Practices. • Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through database lock, ensuring relevant timelines and quality deliverables are met. • Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites. • Monitor site level AEs and SAEs and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to resolution. • Serve as a point of contact for audit conduct, and drive Audit Observation CAPA development and checks, when applicable