Clinical Research Associate II (Part-Time, Contractor)

Company DescriptionTraverse Health is a real-world evidence provider based in the EU, with operations extending to emerging markets. We specialize in developing innovative digital solutions for the healthcare and life sciences industry. By connecting healthcare organizations with pharmaceutical and biotech industries, we harness the potential of patient data to deliver real-world value, support smarter healthcare decisions, and improve patient outcomes. Our offerings serve a wide range of stakeholders in the healthcare ecosystem, including pharmaceutical, biotech, and medical device companies, CROs, health insurance providers, and more.Role DescriptionAs a CRA/Scientific Research Contractor at Traverse Health, you will help shape and support our evidence-generation work with global life sciences partners. You’ll collaborate with internal teams and external clients to translate clinical needs into clear research tasks, build scientific documentation, and support the development of real-world evidence. This is a part-time, flexible role, approx. 10–20 hours/week depending on workload.Key Responsibilities1. Research Project Development & SupportSupport development of study synopses, protocols, and observational study frameworksAssist with real-world evidence (RWE), epidemiology, and medical analytics projectsEnsure study methodologies align with GCP, ICH, and local regulatory frameworks2. Scientific Documentation & ReportingPrepare and maintain key research documents:Study ProtocolsStatistical Analysis Plans (SAPs)Timelines & Progress ReportsFinal Study ReportsContribute to ethics submissions, regulatory documentation, and compliance materials3. Medical Content & Dashboard SupportProvide clinical input for medical, scientific, and market access dashboardsWork with data science teams to interpret clinical requirements and validate outputsSupport creation of summaries, presentations, and scientific insights4. Client Collaboration & Cross-Functional LiaisonTranslate client needs into clear research tasks and deliverablesParticipate in internal meetings and provide clinical/methodological insightsHelp maintain alignment between client expectations and internal executionQualifications:Background in Medicine, Pharmacy, Public Health, Biological Sciences, or related fieldExperience in clinical research, scientific writing, RWE, or medical affairsStrong understanding of clinical study design, protocols, and research methodologyExcellent scientific writing and documentation skillsFamiliarity with GCP, ICH, and basic regulatory conceptsAbility to work independently in a fast-paced, globally distributed teamFluency in English (Spanish or Portuguese is a plus)