• Provide study oversight as the primary liaison between CRAs, internal staff, study site staff including investigators, coordinators, client personnel, and external vendors involved in all stages of the study • Ensure clinical monitoring activities of the study CRA team(s) are performed in accordance with applicable Standard Operating Procedures (SOP), regulations, good clinical practices, key performance indicators, and study-specific requirements • Develop, review, and manage clinical plans and guidelines, including the clinical monitoring plan and study timelines; ensure compliance with monitoring intervals according to project requirements, review data reports, CTMS, disseminate listings/reports to study CRAs, and work with CRAs and site staff to resolve data discrepancies • Create annotated visit report templates and other documents and strategies related to site management and monitoring • Support training and development of team members, ensure compliance with study specific training requirements, and ensure training is appropriately documented • Guide and support CRAs, CTAs, and external contract research organizations regarding monitoring, co-monitoring, training, and audit visits; review site visit reports and monitoring letters in accordance with study and SOP requirements • Manage oversight of the Trial Master File (TMF)/eTMF and assist with filing and quality control • Track serious adverse events, protocol deviations, enrollment, ICFs, study contacts, investigational supplies, and investigational product for assigned study and review with appropriate members of the study team • Perform qualification, initiation, interim, and close out visits and provide visit reports as per monitoring guidelines as needed

• Own the end-to-end execution of quantitative research projects, supporting stakeholders through the full research lifecycle—from survey design and programming to data analysis, reporting, and insight development. • Manage multiple projects simultaneously, ensuring high-quality deliverables, accurate data processing, and timely communication of project progress. • Develop survey questionnaires aligned with research objectives and business questions. • Apply survey design best practices, including question clarity, logical flow, and bias mitigation. • Program surveys using platforms such as Qualtrics, Decipher, or similar survey tools. • Conduct comprehensive quality assurance (QA) testing to ensure survey functionality and respondent experience. • Clean, validate, and prepare survey datasets for analysis. • Create research reports, presentations, and summaries that communicate key findings effectively.

• As a Market Research Analyst, you will own the end-to-end execution of quantitative research projects, supporting stakeholders through the full research lifecycle—from survey design and programming to data analysis, reporting, and insight development. • You will manage multiple projects simultaneously, ensuring high-quality deliverables, accurate data processing, and timely communication of project progress. • This role requires strong expertise in survey methodology, survey programming, data analysis, and reporting, along with exceptional attention to detail and the ability to translate complex findings into clear, actionable business insights.

• Act as the primary site contact and site manager throughout all phases of a clinical research study • Develops strong site relationships and ensures continuity of site relationships through all phases of the trial • Performs clinical study site management/monitoring activities in compliance with International Conference on Harmonization / Good Clinical Practices • Gains an in-depth understanding of the study protocol and related procedures • Participates and provides inputs on site selection and validation activities • Conducts site visits including but not limited to validation visits, initiation visits, monitoring visits, closeout visits • Communicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, and regulatory documentation • Identifies, assesses, and resolves site performance, quality or compliance problems