Act as primary representative for eClinical Solutions and sponsor data management interaction, ensuring quality and timelines within scope.
Define specifications and collaborate with technical teams on configuration of elluminate for data cleaning strategy and oversight.
Perform quality oversight and data trending via elluminate reporting to identify risks and develop mitigation strategies.
eClinical Solutions helps life sciences organizations accelerate clinical development initiatives with expert data services and the elluminate Clinical Data Cloud. The company is a people-first organization with an inclusive culture, recognized as a 2025 Top Workplaces USA Award winner for Remote Work.
Design, develop, and validate CDISC-compliant SDTM and ADaM datasets for clinical trials.
Support regulatory submissions including ISS, ISE, and create Tables, Listings, and Figures.
Collaborate with cross-functional teams to deliver accurate statistical outputs for evidence-based healthcare.
The partner company is a clinical research organization that supports impactful clinical programs through statistical programming. It offers a collaborative culture and a flexible remote work environment.
Serve as the Clinical Scientist for one or more Phase 2/3 studies, contributing to study design, protocol development, and oversight.
Lead data review and medical monitoring activities, identifying trends, deviations, and safety signals in collaboration with Medical Monitors.
Support regulatory submissions, cross-functional partnerships, and scientific publications to advance clinical development.
Jade Biosciences is a clinical-stage biotechnology company focused on developing best-in-class therapies for autoimmune diseases. It is a growing company with a collaborative, fast-paced environment where individual contributions have significant impact.
Design and drive real world evidence studies, including retrospective cohort analyses and claims-linked outcomes, owning each from research question to final deliverable.
Partner with data science to structure analytic datasets from Oura member data and linked claims, producing rigorous and actionable outputs.
Shape research findings into outputs for diverse audiences, including payer briefs and white papers, to advance clinical credibility.
Oura empowers individuals to understand their readiness, activity, and sleep quality through their award-winning Oura Ring and app. A growing company focused on health, they prioritize team well-being and have helped millions improve their health with daily insights.
Manage clinical elements of trials including site selection, start-up, enrollment, monitoring, and close-out for studies across multiple countries.
Lead CRAs and ensure timeline adherence, quality delivery, and effective communication with cross-functional teams and sponsors.
Identify risks to project timelines, create action plans, and mentor team members while maintaining focus on study priorities.
Precision for Medicine is a precision medicine CRO that combines novel clinical trial designs, biomarker and data analytics, with a focus on rare diseases and oncology. The company is part of Precision Medicine Group, a growing organization dedicated to advancing oncology development and positively impacting patient health.
Lead integrated evidence-generation and publication strategies across the company's portfolio.
Identify evidence gaps and develop research plans to disseminate clinical, real-world, and economic data.
Partner with cross-functional teams including Medical Affairs, Clinical Development, and Regulatory to align on scientific priorities.
Freenome is a biotechnology company developing cancer screening tests using multiomics and liquid biopsy. As a growing organization, they emphasize diversity, equity, and inclusion in a collaborative culture.
Leads statistical activities for clinical studies in oncology.
Authors statistical sections of study protocols, analysis plans, and regulatory documents.
Collaborates with cross-functional teams and CROs to ensure high-quality deliverables.
Iovance Biotherapeutics develops tumor infiltrating lymphocyte (TIL) therapy for cancer treatment. The company is a global leader in cell therapy innovation with a focus on clinical data and regulatory submissions.
Lead analysis and interpretation of cancer's molecular signatures, guiding model development for biological changes.
Execute rigorous computational analyses on data from high-throughput molecular assays including sequencing and protein quantitation.
Partner with molecular biologists and development scientists to refine experiments and turn research models into products.
Freenome is a biotechnology company developing blood tests for early cancer detection. We are a growing organization dedicated to changing the landscape of cancer, with a collaborative and diverse team.
Own CMC oversight across every active asset, ensuring on-time and on-budget delivery of drug substance, drug product, analytics, stability, and regulatory filings.
Select, contract, and manage CDMOs and external partners, holding them to timelines, quality, and cost.
Scope and de-risk the CMC of inherited in-licensing candidates, flagging manufacturing complexity or cost that could affect asset viability.
Our mission is to fix the broken clinical-stage biopharma model by in-licensing therapeutic assets and developing them through integrated, technology-first clinical trial infrastructure. We are a new initiative built on a proven foundation, with a team that has delivered 40+ trials across the US and Europe, and we are a high-growth, mission-driven, VC-funded startup.
Provide technical leadership in genomic surveillance, analytics, and antimicrobial resistance for global health security initiatives in Sierra Leone.
Support strengthening of detection capacity and laboratory systems for human and animal health networks.
Contribute to design, implementation, and monitoring of strategies aligned with global best practices and national policies.
PSI is a globally connected organization working to achieve consumer-powered healthcare, focusing on people-centered health systems. With over 50 years of experience, it has developed innovative solutions to complex global health challenges and operates as a network of locally rooted entities.