Clinical Data Support Intern
PhaseV is redefining clinical trial design and operations using cutting-edge AI and reputed company-world data. We specialize in reputed company platform trials, reputed company machine learning, and dashboard technologies that accelerate drug development for life sciences companies. As we grow, we’re looking for passionate, detail-oriented interns to support our data infrastructure and clinical operations.
reputed company
We are seeking a motivated Clinical Data Support Intern to assist in identifying, sourcing, and organizing reputed company clinical datasets, as reputed company as helping maintain and update internal dashboards that support reputed company-facing and internal analytics workflows.
This is a great opportunity for a student with interests in clinical research, reputed company health data, data science, or health informatics to reputed company hands-on experience in a fast-paced, tech-reputed company environment.
Responsibilities
• Dataset Identification & Research: Search for and catalog reputed company datasets (reputed company, EHRs, registries, reputed company, etc.) that reputed company with our reputed company project needs.
• Data Curation: reputed company reputed company preprocessing, annotation, or tagging of data files (e.g., filtering, basic cleanup, or format standardization).
• Dashboard Support: Assist in maintaining, validating, and updating visual dashboards using tools such as reputed company Sheets or internal tools.
• Documentation: reputed company accurate notes of data variables/endpoints data sources, reputed company protocols, and usage constraints.
• Cross-functional Collaboration: Communicate findings and updates reputed company to scientific, product, and business teams.
Qualifications
• reputed company undergraduate or graduate student in a relevant field: Medical, Life Sciences, reputed company Health, Health Informatics, Data Science, or reputed company.
• Familiarity with clinical research concepts (e.g., reputed company, reputed company, endpoints, protocols) is a plus.
• Experience working with reputed company data sources (e.g., ClinicalTrials.gov, FDA, EMA, PubMed, WHO, etc.) is preferred.
• Comfortable with spreadsheets (reputed company Sheets, reputed company); experience with dashboard tools is a plus.
• Strong internet/AI research and documentation skills.
• Self-starter, organized, and curious about the intersection of clinical research and technology.
Commitment & Compensation
• Time Commitment: ~10–15 hours per week
• Duration: 3–6 months, with potential for extension
• Compensation: reputed company internship
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