Plan and execute development experiments for Freenome's multiomics cancer screening tests.
Partner cross-functionally with computational, development, regulatory, and quality teams to develop a regulated strategy toward FDA approval.
Use quantitative skills to develop computational methods and interpret complex experimental results to optimize and validate innovative technology.
Freenome is a biotechnology company developing early, noninvasive blood-based tests for cancer detection. The company emphasizes a highly collaborative, cross-functional environment and values diversity.
Oversee evidence-generation strategy and manage research studies for the da Vinci Cardiac Surgery Program.
Collaborate with stakeholders to identify evidence gaps, align priorities, and develop evidence-generation plans.
Manage CROs, research partners, and publications while ensuring regulatory compliance and audit readiness.
Intuitive is a global leader in robotic-assisted surgery and minimally invasive care, with technologies like the da Vinci system transforming care for millions worldwide. We are a team of engineers, clinicians, and innovators united to make surgery smarter, safer, and more human.
Lead ongoing clinical data review to ensure quality, interpretation, and patient safety across development programs.
Develop and review study protocols, investigator brochures, and regulatory documents in partnership with cross-functional teams.
Represent Clinical Development on study teams and present clinical data and scientific information to internal and external audiences.
Deciphera, a member of Ono Pharmaceutical Co., Ltd., is a biopharmaceutical company discovering, developing, and commercializing new medicines for cancer, neurologic, and autoimmune disease. They cultivate an inclusive culture valuing curiosity, creativity, and shared accountability, empowering individuals to challenge the unknown together.
Drive end-to-end execution of multimodal genomics studies from experimental design through data delivery.
Plan and execute single-cell RNA-seq, spatial transcriptomics, and spatial proteomics experiments including sample preparation and QC.
Support external BioPharma collaborations and lead internal discovery experiments to translate complex datasets into biological insight.
Natera is a global leader in cell-free DNA testing, dedicated to oncology, women's health, and organ health. The company brings together highly dedicated scientists, geneticists, and other professionals to make personalized genetic testing part of standard care.
Provide strategic leadership and operational oversight for clinical trial design, analysis, and reporting.
Build and mentor a high-performing clinical biostatistics team while driving regulatory submissions.
Partner with cross-functional teams and vendors to ensure high-quality statistical and data management support.
Enveda is a clinical-stage, AI-enabled biotech discovering medicines from nature four times faster than industry standard. With over $845M in total funding and a $2B valuation, the company is recognized as a top startup employer and has three oral medicines in the clinic.
Monitor clinical trial sites to ensure ethical, safe, and compliant conduct per protocol, GCP, and regulations.
Serve as primary liaison between Lycia and investigative sites for startup, maintenance, and close-out activities.
Manage regulatory documents, EDC data queries, and remote monitoring to maintain audit-ready TMF and CTMS records.
Lycia Therapeutics is a clinical-stage biotechnology company developing LYTAC-based therapeutics to degrade disease-driving proteins. It went public in 2026 and is headquartered in South San Francisco, California.
Create custom educational documents for cancer patients in collaboration with oncology nurse navigators.
Enhance the research base on cancer types by identifying gaps and performing deep dives into clinical literature.
Execute clinical research projects autonomously, mastering complex medical content quickly.
CancerNavigator is an early-stage healthcare company providing white-glove, end-to-end cancer support services to patients via Oncology Certified Nurses. The company is remote-first, headquartered in Washington, D.C., and values patient-first culture and team collaboration.
Independently manage assigned clinical trial activities in compliance with GCP and regulations.
Oversee essential study documentation, TMF completeness, and study trackers.
Manage vendors, CTMS activities, and cross-functional coordination to ensure compliant study execution.
Cognito Therapeutics is a neurotechnology company developing a new therapeutic approach to cognitive and neurological health, including an investigational therapy for Alzheimer's disease. The company is an interdisciplinary team united by a shared purpose of protecting and progressing the human ability to think, learn and remember.
Lead the development and execution of industry-sponsored research and quality improvement programs.
Collaborate with internal and external stakeholders to drive strategic partnerships and evidence generation.
Oversee project budgets, timelines, and cross-functional teams to ensure successful delivery.
The American Heart Association is a nonprofit organization dedicated to fighting heart disease and stroke through research, education, and advocacy. It is a large national organization with a culture focused on work-life harmonization and employee well-being.
Perform on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visits to ensure sites are adequate for study conduct.
Verify investigator qualifications, resources, facilities, equipment, and staff for clinical study conduct.
Train site staff, support regulatory/EC submissions, and mentor junior staff during co-monitoring visits.
Ergomed Group is a global clinical research organization helping biopharmaceutical companies develop and deliver therapies in oncology, rare disease and other complex areas. Its diverse teams across countries and time zones collaborate with kindness, curiosity and a shared sense of purpose.