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.
Lead research efforts on complex care cases, including reviewing medical records and clinical history.
Identify and evaluate diagnostic and treatment options, including clinical trials and innovative therapies.
Communicate research findings to clients and clinicians to support shared decision-making.
Private Health Management is a healthcare navigation firm that assists clients with serious and complex medical conditions. The company operates remotely across the United States with a team of compassionate, dedicated professionals focused on precision medicine.
Define and oversee Toxicology and Non-Clinical Pharmacology strategies for assigned projects.
Serve as the subject matter expert in Toxicology, managing preclinical safety studies and regulatory interactions.
Ensure translational aspects and safety alerts are integrated into benefit/risk assessments.
A biopharmaceutical company dedicated to developing innovative therapies for rare diseases. With over 1,900 employees in more than 30 countries, Sobi fosters a culture of inclusion and empowerment.
Provide strategic statistical leadership across oncology development programs, collaborating with Clinical Development, Regulatory, Medical, Commercial, and Portfolio teams.
Design and validate trial types, endpoints, and innovative adaptive designs while performing sample size/power calculations and establishing go/no-go decision gates.
Support regulatory submissions and health authority interactions, and quantify technical success probability for pipeline prioritization.
We are a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 4,000 professionals in more than 20 countries, we are committed to training, diversity, and accelerating innovative drug and device development.
Evaluate AI-generated responses for scientific accuracy and logical consistency.
Test AI models with theoretical biology questions and realistic laboratory scenarios.
Identify and document model failure modes, recommending improvements to prompts and evaluation methods.
A partner company of Jobgether focused on improving AI language models through expert scientific training and evaluation. The organization works with freelance specialists to enhance AI reasoning and reliability in biological domains.
Define expert reasoning for peptide discovery and write gold-standard answers with defended rationale.
Curate datasets from real programs and build Python analysis pipelines that produce verifiable ground truth.
Test and challenge AI agents' reasoning, scoring confidence and pinpointing where they go wrong.
Latch builds rigorous scientific benchmarks for AI agents across biology, working with frontier labs and pharma to measure real biological workflows. It's a transparent startup that uses AI constantly and rewards original expert judgment.
Lead the clinical development of respiratory disease programs, overseeing study design, execution, and delivery across the development lifecycle.
Provide scientific oversight to ensure patient safety, study quality, and timely delivery while generating and interpreting clinical evidence.
Collaborate with cross-functional teams and external stakeholders to align clinical strategies with regulatory, commercial, and patient needs.
They are a pharmaceutical company focused on advancing clinical research and developing innovative treatments for respiratory diseases. The organization fosters an inclusive, collaborative culture that prioritizes patient impact, professional growth, and scientific innovation.