Non-Resident Research Fellow, Religious Liberty Clinic, Stanford Law School Stanford UniversityNon-Resident Research Fellow, Religious Liberty Clinic, Stanford Law SchoolStanford, CA$54,416–$98,067 / yearpreferred) or distinguished undergraduate degree, with experience relevant to the RLCs work and the described project; a developed interest in religious liberty and commitment to the RLCs program of clinical legal education; strong and relevant research skills and experience; first-rate writing abilities; a commitment to teamwork and collaboration; sound judgment and integrity; and strong organizational and project-management skills, attention to detail, ownership, and motivation. This is a rare opportunity for a recent law-school graduate or particularly distinguished college graduate to conduct and support research in one of the nations premier law-school clinics at one of the worlds preeminent institutions for legal education, and to gain valuable professional experience in a dynamic environment while serving the public interest.
Assistant, Associate or Full Professor for Ophthalmology (Research) stanfordAssistant, Associate or Full Professor for Ophthalmology (Research)Palo Alto, CaliforniaThe pay offered to the selected candidate will be determined based on factors including (but not limited to) the experience and qualifications of the selected candidate including equivalent years in rank, training, and field or discipline; internal equity; and external market pay for comparable jobs. The Ophthalmology, School of Medicine, and Stanford University value faculty who will help foster an open and respectful academic environment for colleagues, students, and staff with a wide range of backgrounds, identities, and perspectives.
Research Program Administrator - Heart Institute - Cheng Lab Cedars-Sinai Medical CenterResearch Program Administrator - Heart Institute - Cheng LabLos Angeles, CAOur cardiologists, cardiac surgeons and niche care teams treat the full spectrum of heart disease and disorders, while our investigators continue to advance the field with groundbreaking, life-saving research. From genetic counseling and targeted drug therapies to an increasing array of minimally invasive procedures, Cedars-Sinai continues to stand at the forefront of technology, innovation and discovery improving patient outcomes.
Associate Director Aesthetics Clinical Development AbbVie IncAssociate Director Aesthetics Clinical DevelopmentIrvine, CAResponsibilities: Under supervision of the Global Clinical Development Lead, designs, directs, executes, and interprets clinical trials/research and data collection activities in support of the overall Product Development Plan, within time, budget, and based on strong scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations and emerging issues. Responsible and accountable for the scientific validity, integrity and overall quality of the Clinical Development Plan and all clinical content, including, but not limited to protocols, IBs/IDFUs, clinical data reviews, CSRs, regulatory submissions, and publications associated with the clinical trials.
Sr. Manager, Clinical Operations 10X Genomics IncSr. Manager, Clinical OperationsPleasanton, CA$173,100–$234,100 / yearKey responsibilities for this role include: managing a portfolio of academic collaborations and strategic partnerships according to established milestones and outcomes, leading the operational execution for large-scale, multi-year collaborations with premier academic institutions to generate evidence for future clinical applications of single-cell and spatial technologies, and driving collaboration between internal cross-functional teams and external partners to achieve desired results. Manager, Clinical Operations reporting to the Director, Business Development and Strategic Partnerships will drive the operational execution and strategic management of high-impact alliances central to 10x Genomics' effort to advance future diagnostic applications for single cell and spatial technologies.
NewResearch Associate I Veracyte IncResearch Associate ISouth San Francisco, CA$36–$40 / hourOur 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 ideal candidate is excited to build hands-on experience with molecular biology and NGS technologies while contributing to innovative diagnostic products in a collaborative and fast-paced product development environment.
Anesthesiology - Vice Chair of Research Cedars-Sinai Medical CenterAnesthesiology - Vice Chair of ResearchLos Angeles, CA$545,896–$714,043 / yearThe total pay range shown takes into account the wide range of factors that are considered in making compensation decisions including knowledge/skills; relevant experience and training; education/certifications/licensure; and other business and organizational factors. Cedars-Sinai Medical Center, a state-of-the-art, 958 bed tertiary acute care academic medical center is committed to excellence in compassionate patient care, research, education, and community programs to improve the lives of our patients.
Research Lab Technician II Keck Medicine of USCResearch Lab Technician IILos Angeles, California$24.50–$26.55 / hourWhen extending an offer of employment, the University of Southern California considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate’s work experience, education/training, key skills, internal peer equity, federal, state, and local laws, contractual stipulations, grant funding, as well as external market and organizational consideration. The successful candidate should have: 1) at least 1 year hands-on experienced in basic or clinical research, particularly isolation of primary cells; 2) team-oriented research experience; and 3) excellent oral and written communication skills and work well with people.
Senior Project Manager/Clinical Evaluation Reporting (on-site) AbbottSenior Project Manager/Clinical Evaluation Reporting (on-site)Pleasanton, South Carolina$90,000–$180,000 / yearThe primary function of a Regulatory Project Manager, Clinical Evaluations (“Clinical Evaluation Report (CER) Project Manager (PM)”) is to combine understanding of scientific and research methodology, medical device regulations and guidelines, and product and therapeutic area knowledge to support Regulatory Affairs medical device submissions in the EU for CE Marking of new devices and maintaining of CE Mark for existing devices in accordance with EU MDR 2017/745, MEDDEV 2.7/1 Rev 4, MDCG Guidance documents, and predicate MDD and AIMDD directive requirements. Facilitate communication and exchange of documents between stakeholders (e.g., internal personnel such as Regulatory Affairs, R&D, Clinical R&D, A&P and Marketing, Library Services, Quality Engineering, Clinical Affairs, Risk Management, Program Management, as well as external vendors such as CROs, Medical Writers and Physician Reviewers).
Senior Project Manager/Clinical Evaluation Reporting (on-site) Abbott LaboratoriesSenior Project Manager/Clinical Evaluation Reporting (on-site)Pleasanton, CA$90,000–$180,000 / yearThe primary function of a Regulatory Project Manager, Clinical Evaluations ("Clinical Evaluation Report (CER) Project Manager (PM)") is to combine understanding of scientific and research methodology, medical device regulations and guidelines, and product and therapeutic area knowledge to support Regulatory Affairs medical device submissions in the EU for CE Marking of new devices and maintaining of CE Mark for existing devices in accordance with EU MDR 2017/745, MEDDEV 2.7/1 Rev 4, MDCG Guidance documents, and predicate MDD and AIMDD directive requirements. Facilitate communication and exchange of documents between stakeholders (e.g., internal personnel such as Regulatory Affairs, R&D, Clinical R&D, A&P and Marketing, Library Services, Quality Engineering, Clinical Affairs, Risk Management, Program Management, as well as external vendors such as CROs, Medical Writers and Physician Reviewers).
NewClinical Programmer II ReCor Medical IncClinical Programmer IIPalo Alto, CA$122,857–$132,796 / yearMaster's degree in computer science, data science, statistics, life sciences, or related field with 1+ years of experience; or a Bachelor's degree in these fields with 2+ years of professional experience in Clinical Programming, data visualization, business intelligence, or analytics roles. Support clinical operational activities by developing and maintaining tools for tracking study progress, site performance, and other key operational metrics, including generating regular reports and dashboards to provide insights into clinical trial operations.
Sr. Manager Clinical Research Engineering Intuitive Surgical IncSr. Manager Clinical Research EngineeringSunnyvale, CAHire, develop and mentor CREs for the program, Presents findings to key opinion leaders, subject matter experts, physicians, and other stakeholders to identify clinical goals and translate those needs for user-centric design and development of new platforms, procedures, instruments, and accessories. Manager Clinical Research Engineering uses their in-depth clinical, scientific, and technical knowledge to lead, collaborate with engineers, physicians, user experience researchers, and other internal and external stakeholders to develop new product concepts being incubated in early exploration.
Clinical Trial Manager Revolution Medicines, Inc.Clinical Trial ManagerRedwood City, CA$120,000–$150,000 / yearThe company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. The Opportunity: This is a unique opportunity for an experienced Clinical Operations Professional who has technical expertise in managing Phase I-III clinical trials in an industry setting and a strong knowledge of clinical operations, Good Clinical Practice (GCP) and U.S. Food and Drug Administration (FDA) regulatory requirements.
Associate Director, Clinical Biomarker Development Revolution Medicines, Inc.Associate Director, Clinical Biomarker DevelopmentRedwood City, CA$186,000–$233,000 / yearThe company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. The Opportunity: The Associate Director in Clinical Biomarker Development team, within Translational Medicine will play a key role in the design, execution, and interpretation of clinical biomarker strategies across Revolution Medicine's oncology pipeline.
Director, Clinical Business Operations & Strategic Vendor Management Enigma SearchDirector, Clinical Business Operations & Strategic Vendor ManagementCaliforniaWe are seeking an experienced Director of Clinical Business Operations & Strategic Vendor Management to lead outsourcing strategy, vendor governance, and business operations across Phase 2 and Phase 3 clinical development programs. This role will partner closely with Clinical Operations, Finance, Legal, Quality, and other cross-functional teams to ensure efficient study execution through effective vendor selection, contracting, oversight, and financial management.
Oracle Life Sciences- Sr. Research Consultant- Neurology Oracle CorpOracle Life Sciences- Sr. Research Consultant- NeurologyCA$74,100–$148,300 / yearWith ongoing and ground-breaking developments in Neurology, Oncology and Rare Disease, an increased focus on more scientific, targeted medicine and continuous integration of technology into development and delivery of medicine, there has never been a more exciting time to work in Life Sciences and there has never been a better time to join us and make a difference to our clients and the lives of patients. Oracle maintains broad salary ranges for its roles in order to account for variations in knowledge, skills, experience, market conditions and locations, as well as reflect Oracle''s differing products, industries and lines of business.
NewClinical Educator School of Education Supporting Pacific and Mountain Time Zones Western Governors UniversityClinical Educator School of Education Supporting Pacific and Mountain Time ZonesCA$60,600–$90,900 / yearThe Clinical Educator plays an important role in helping candidates balance the duties and responsibilities of Advanced Clinicals while learning to navigate and understand the complex world of educational practice. A Clinical Educator is an experienced educator who acts as a subject matter advisor and guide to a group of WGU teacher candidates prior to, during, and following the Advanced Clinicals experiences.
Licensed Outpatient Therapist and Clinical Supervisor Mission EdgeLicensed Outpatient Therapist and Clinical SupervisorSan Diego, CA$50–$60 / hourEFFECT ON END RESULT: This position ensures that specialty mental health services and clinical supervision are provided in a trauma-informed and culturally respectful manner to support the care and treatment of clients within the Casa de Amparo outpatient program embedded at TrueCare. This recruitment effort is proudly supported by Mission Edge, partnering with Casa de Amparo to connect passionate individuals with meaningful opportunities in child welfare and residential care.
Specialist, Clinical Trials Neurocrine Biosciences Inc.Specialist, Clinical TrialsSan Diego, CA$89,800–$123,000 / yearThe company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in Prader-Willi syndrome, endometriosis and uterine fibroids , as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. Collaborates with clinical research colleagues within Neurocrine, at Contract Research Organizations (CROs), and at Investigator sites to conduct clinical trials adhering to Good Clinical Practice (GCP) and ensuring accurate data, subject safety and impeccable documentation.
Research Engineer - Data Quality & Evals Epsilon LabsResearch Engineer - Data Quality & EvalsSan Francisco, CaliforniaBuild data filtering and curation pipelines that keep VLM and classifier training sets clean, detecting label noise, misaligned image-report pairs, duplicates, corrupted studies, and low-quality samples at scale. Design evaluation methodology for report generation that goes beyond surface-level text overlap, measuring clinical accuracy through entity and relation extraction, hallucination and omission rates, and adherence to reporting style.