Assess information and knowledge-based needs to inform clinical system design and optimization.
Develop, implement, and refine clinical decision support systems and electronic health records.
Collaborate with clinical staff and IT teams to ensure system implementations meet objectives.
Ibility is a Service-Disabled Veteran-Owned and Woman-Owned Small Business that helps government leaders achieve their mission by designing creative products and programs with human-centered design principles. It is a small but rapidly growing company with a passionate and bold team.
Oversee strategic and operational execution of clinical trials, leading cross-functional teams and managing vendor selection.
Direct clinical trial budgets, risk mitigation, and provide technical input into key clinical documents.
Mentor staff and foster strong team relationships in a dynamic organization.
Jade Biosciences is a clinical-stage biotechnology company developing best-in-class therapies for autoimmune diseases. The company was launched based on assets licensed from Paragon Therapeutics and has a growing pipeline.
Oversee critical monitoring activities across clinical trials, ensuring compliance with protocols and regulations.
Collaborate with investigators and site teams to maintain study integrity and operational excellence.
Support Phase II and Phase III trials in challenging therapeutic areas to improve patient outcomes.
Jobgether uses artificial intelligence to match job seekers with opportunities through a fair and efficient process. As a growing platform, they emphasize collaboration, integrity, and patient impact in their culture.
Oversee clinical site management and ensure compliance with protocols, regulations, and quality standards.
Serve as primary contact for study sites, conducting monitoring visits from pre-study through close-out.
Collaborate with cross-functional teams to support data review, regulatory submissions, and site performance.
Our partner is a global clinical research organization managing monitoring activities across Phase I–IV trials and Real World Evidence studies. It offers a collaborative, fully remote environment focused on improving patient outcomes with professional growth opportunities.
Inspire and lead the Medical Affairs function, guiding MSLs and teams while fostering trusted scientific relationships with KOLs and stakeholders.
Oversee medical information, medical education, HEOR, publication planning, lifecycle management, and launch strategy.
Partner cross-functionally on the Promotional Review Committee, ensuring compliance and scientific rigor.
ARS Pharmaceuticals is a fast-growing, innovative company dedicated to transforming the treatment of severe allergic reactions with neffy, the first FDA-approved needle-free epinephrine product. Headquartered in San Diego, CA, the company fosters a collaborative, entrepreneurial, and inclusive culture with a commitment to improving patients' lives.
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.
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.
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.