Lead data management activities from study start-up to database lock, ensuring quality and timelines.
Act as subject matter expert for DM in sponsor meetings and implement process improvements.
Mentor and train junior DM staff while managing project documentation, data validation, and system setup.
Fortrea is a global contract research organization providing clinical development and biometrics services to pharmaceutical and biotechnology companies. With a focus on teamwork and excellence, they foster a family-like culture where employees collaborate to advance life-saving therapies.
Contribute to the technical approach for evaluating AI agent performance across the genetic medicines pipeline, including gene therapy, gene editing, and RNA therapeutics.
Design realistic program case studies spanning target validation, drug design, screening, chemistry optimization, and IND-enabling studies.
Review and stress-test AI agent outputs for scientific soundness, calibrating confidence on preclinical data with incomplete or conflicting signals.
Latch builds rigorous scientific benchmarks for AI agents across biology, working with frontier labs and pharma to measure whether agents can handle real biological workflows. The culture emphasizes radical transparency, high agency, and using AI tools with original expert judgment.
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.
Design challenging scientific evaluations that test AI agents' reasoning in human physiology.
Analyze real experimental, clinical, and physiological data to establish reliable ground truth.
Collaborate across disciplines, using AI-assisted tools to accelerate benchmark development.
Latch builds rigorous scientific benchmarks for AI agents across biology, working with frontier labs and pharma to measure real biological workflows. They practice radical transparency, reward original expert judgment, and foster a community with outings, off-sites, and shared activities.
You will shape how AI agents are evaluated in immunology by contributing to the technical approach and benchmark design.
You will build ground-truth datasets from studies, your own experience, and novel work to test expert-level reasoning.
You will collaborate with software engineers and computational biologists to rigorously measure agent performance on real biological tasks.
Latch builds rigorous scientific benchmarks for AI agents in biology, working with frontier labs and pharma to measure real biological workflows. The culture emphasizes radical transparency, heavy AI use, and original expert judgment, with a collaborative team that enjoys outings, sports, and game nights.
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.
Lead site feasibility, SIVs, routine monitoring, and close-out visits in line with GCP and regulatory requirements.
Build strong relationships with site staff, verify source data, and ensure inspection-ready documentation.
Support study document design, data query resolution, and train or coordinate other CRAs.
WEP Clinical partners with biopharmaceutical sponsors to bring treatments to patients via clinical trials, home health, expanded access, and market access services. With 15+ years and 150+ countries, it offers a collaborative, mission-driven culture focused on innovation and growth.
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.