div class="content">About N-Power Medicine
N-Power Medicine aims to establish a new paradigm in drug development by reinventing the ‘how’ and transforming clinical trials through better integration with clinical practice, ensuring broader participation by physicians and patients. As the Digital Health Specialist II (internal title), you will work at a clinical site in Los Gatos, CA.
The ideal candidate has clinical oncology research experience or research experience in a healthcare setting.
The Cardinal at Work website (https://cardinalatwork.stanford.edu/benefits-rewards) provides detailed information on Stanfords extensive range of benefits and rewards offered to employees. The pay offered to a selected candidate will be determined based on factors such as, but not limited to, the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location, and external market pay for comparable jobs.
Desired: Coursework and/or knowledge of molecular biology, biomedical engineering, computational biology, programming; - Experience working with predictive modeling; - Experience working in a research environment; - Computational biology experience and coding in R/Python - Understanding of basic molecular biology and stem cell biology; - Some knowledge of research procedures and protocols gained through education or experience; - Knowledge of scientific research methodology and data analysis skills; - Strong reasoning skills in order to troubleshoot experiments; - Ability to grasp concepts in scientific papers for key methods or findings to support research; - Ability to work in a team; - Ability to multi-task several projects at the same time. The Life Sciences Research Assistant will support ongoing research projects that study stem cell and tissue engineering approaches to treat vascular disease and muscle injury.
li>Manage clinical research data and study operations, including developing data collection systems, extracting and analyzing study data, creating project schedules, tracking milestones, leading team meetings, and maintaining study documentation. Clinical Research Coordinator Responsibilities:
- Oversee subject recruitment, enrollment, and retention activities for clinical studies, developing effective strategies to meet enrollment goals and supporting participants throughout long-term treatment trials.
With interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation. Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials.
The Cardinal at Work website (https://cardinalatwork.stanford.edu/benefits-rewards) provides detailed information on Stanfords extensive range of benefits and rewards offered to employees. The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location and external market pay for comparable jobs.
li>Coordinate study operations by developing project schedules, leading team meetings, supervising and mentoring research staff or students, and supporting study budgets, milestone tracking, and sponsor invoicing activities. - Manage subject recruitment, enrollment, and retention activities, and oversee data collection systems, including organizing, monitoring, analyzing, and interpreting study data to support clinical research objectives.
Santa Clara, California30+ days ago
All applicants desiring an accommodation should contact the Department of Human Resources, and 408-554-5750 and request to speak to Indu Ahluwalia by phone at 408-554-5750 or by email at iahluwalia@scu.edu. To view the Santa Clara University report, please go to the Campus Safety Services website .
The Cardinal at Work website (https://cardinalatwork.stanford.edu/benefits-rewards) provides detailed information on Stanfords extensive range of benefits and rewards offered to employees. EDUCATION & EXPERIENCE (REQUIRED):
- Two-year college degree and two years related work experience or a Bachelor''s degree and one year of related work experience or an equivalent combination of related education and relevant experience.
Mountain View, CA23 days ago
Our teams are applying our expertise and technology to improve health outcomes globally - with high-quality information and tools to help people manage their health and wellbeing, solutions to transform care delivery, research to catalyze the use of artificial intelligence for the screening and diagnosis of disease, and data and insights to the public health community. You are highly collaborative and will align with cross-functional, non-clinical teams, such as engineering, product management, legal, privacy, and regulatory affairs, and coordinate with external clinical trial sites, academic collaborators and agreement research vendors.
Belmont, California5 days ago
Responsibilities include conducting daily experiments in behavioral neuroscience and pharmacology using: a) neurochemical assays to determine how drugs and/or environmental stressors induce changes in brain neurotransmitters; b) complex behavior and cognitive assays to characterize how psychoactive drugs and/or environmental stressors impact neurobehavioral processes; and c) physiological assays to determine how drugs and/or environmental stressors alter biological activity. Responsibilities include conducting daily experiments in behavioral neuroscience and pharmacology using a) neurochemical assays to determine how drugs and/or environmental stressors induce changes in brain neurotransmitters b) complex behavior and cognitive assays to characterize how psychoactive drugs and/or environmental stressors impact neurobehavioral processes and c) physiological assays to determine how drugs and/or environmental stressors alter biological activity.
South San Francisco, CA19 days ago
p>Relationship Management & Site Support: Builds deep, multi-stakeholder relationships at strategic sites (including investigators, pharmacists, and administration), acting as a "site champion" and Primary Point of Contact to maintain cross-study consistency and address site needs. Cross-Functional Collaboration & Reporting: Partners seamlessly with internal teams (e.g., Medical Affairs, Study Start-Up) and CROs to ensure unified site communication, while maintaining meticulous documentation of site visits and interactions in central systems (e.g., Veeva).
South San Francisco, CA30+ days ago
Our Veracyte Diagnostics Platform delivers high-performing cancer tests that are fueled by broad genomic and clinical data, deep bioinformatic and AI capabilities, and a powerful evidence-generation engine, which ultimately drives durable reimbursement and guideline inclusion for our tests, along with new insights to support continued innovation and pipeline development. The Position:
The Clinical Research Associate (CRA) Lab Clinical Operations supports the execution of Veracytes clinical research programs, focusing on wet lab testing for clinical studies.
The Company also has a number of preclinical stage drug discovery programs addressing clinically and commercially validated targets including an oral IL-17 peptide antagonist, obesity dual and triple agonists, an oral hepcidin functional mimetic, and the recently announced IL-4 and amylin programs. Serves as the internal primary site operations lead, working with the Project Manager and CROs to achieve efficient study set-up and initiation, ongoing data monitoring all the way through successful study execution and site close-out.
li>Support study vendor management by performing key activities as delegated by study CTM, including but not limited to: Participate in evaluation of new vendors (CROs, labs, central readers, EDC, etc.) by drafting and/or reviewing RFPs, analyzing responses and drafting work orders for select vendors • Manage the day to day interactions with select study vendor(s), such as a central or specialty lab including developing training materials, lab manuals and acting as first point of contact for issue and query escalation and resolution. - Part of the clinical study team and takes a lead on execution by performing key activities as delegated by the Clinical Study lead, including but not limited to:
- Develop and/or review key study operational documents (e.g., study reference manual, laboratory and pharmacy manuals, data management plan, query generation, monitoring plan; review site audit reports) •.
Redwood City, CA5 days ago
This role performs on site and remote monitoring, reviews monitoring reports and site data for quality and trends, supports issue identification and resolution at the site level, and collaborates closely with the clinical study team. The company's platform is already delivering unprecedented insights into the microbial landscape, providing clinicians with a comprehensive test capable of identifying more than a thousand pathogens directly from blood, and helping industry accelerate the development of therapeutic solutions.
Santa Clara, CA30+ days ago
ul>Basic understanding of the following: working safely in a chemical laboratory, principles of chemical reactivity, stoichiometry, chemical synthesis, spectroscopic analysis of molecules (organic/inorganic/organometallic). Synthesize various organic, inorganic, and organometallic molecules using air-free Schlenk and glovebox methods, including calculating reagent amounts and monitoring reaction progress.