Principal Clinical Research Scientist (Hybrid)
$168k - $185kCeribell
About CeribellCeribell is a medical technology company focused on transforming the diagnosis and management of patients with serious neurological conditions. The Ceribell System is a novel, point-of-care electroencephalography (“EEG”) platform specifically designed to address the unmet needs of patients in the acute care setting, and is being used in hundreds of community hospitals, large academic facilities and major IDN's across the country. Our entire team is driven by a shared commitment to transforming the landscape of critical care through our rapid seizure detection technology, come join the movement!Position Overview:The Principal Clinical Research Scientist is responsible for generating, analyzing, and communicating clinical evidence to support product development, regulatory submissions, and commercial growth. This individual combines strong data analysis and scientific writing skills with hands-on conference strategy and marketing activities. This role works closely with clinical operations, regulatory, marketing, R&D teams and external experts (physicians and key opinion leaders) to translate clinical data into publications, presentations, and marketing materials that drive adoption and support clinical decision-making.What you'll do:Own the full lifecycle of clinical evidence generation from gap analysis through literature review, study conception, protocol development, data collection and analysis, to manuscript authorship and publication in peer-reviewed journals.Authoring and presenting scientific communications (abstracts, manuscripts, posters, presentations) for peer-reviewed and commercial audiences at scientific conferences and congresses.Managing the clinical evidence library and publication pipeline, maintaining timelines and coordinating with Regulatory and Marketing on publication and presentation strategy.Supporting regulatory submissions with clinical evidence and results from clinical trials (e.g. FDA 510(k)).Contribute to the design of prospective and retrospective clinical studies on existing and future products, and interface with study investigators, KOL advisors, and internal teams (Data Science, Regulatory, Marketing, Product).Maintaining strong relationships with clinical and scientific leaders (site investigators, principal investigators, KOL advisors) to advance study execution, analysis and results dissemination.Developing and executing conference activities for major medical meetings, including abstract/presentation submissions, KOL engagement, and investigator coordination.Work in close partnership with Marketing, Sales, and Go-to-Market teams to drive the development of clinical evidence summaries, infographics, and data visualizations, guaranteeing scientific integrity, data accuracy, and regulatory compliance.Other responsibilities as assigned by your Manager/Supervisor What We're Looking For: PhD in Clinical Research, Engineering, Epidemiology, Biostatistics, Public Health, or related life science discipline5 + years of clinical research experience in the medical device or pharmaceutical industryProficiency in statistical analysis (R, Python, or equivalent)Strong scientific writing and experience writing peer-reviewed journal articles Demonstrated ability to analyze and interpret clinical dataExcellent written and verbal communication skills; ability to translate complex clinical data for diverse audiences (clinicians, regulators, commercial teams)Preferred qualifications:8+ years of clinical research experience in the medical device industryNeuroscience expertiseClinical trial or clinical data study design experienceTo complete your application, please upload a document containing a comprehensive list of your publications alongside your resume.Compensation Range$168,000—$185,000 USDA candidate’s final salary offer will be based on their skills, education, work location and experience, and thus it may differ from the posted range. Compensation may also include bonuses consistent with Ceribell’s corporate compensation plan. Note, the above description is not all-encompassing and Ceribell reserves the right to change or modify job duties and assignments at any time.In addition to your base compensation, Ceribell offers eligible employees the following:Performance-based incentive compensation (varies by role)Equity opportunities100% Employer paid Health Benefits for Employees50% - 70% Employer paid Health, Dental & Vision for dependents (depending on plan selection)100% paid Life and Long-Term Disability Insurance 401(k) with a generous company matchEmployee Stock Purchase Plan (ESPP) with a discountMonthly cell phone stipendFlexible paid time off13 Paid Holidays + 3 Company Wellness DaysExcellent parental leave policyFantastic culture with tremendous career advancement opportunitiesJoining a mission-minded organization!Application Deadline: OngoingOther Job DetailsCeribell reports transfers of value to health care providers (HCPs) as required by federal and state transparency laws. These laws and implementing regulations require Ceribell to provide government agencies with HCPs’ names, addresses and the type of payments or other value received, generally for public disclosure. If you are an HCP and we pay or reimburse your recruiting expenses as a result of interviewing with Ceribell, your name, address and the amount of payments made may be reported to the government.Equal Opportunity EmployerCeribell is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity or expression, national origin, age, marital status, disability, veteran status or any other characteristic protected by law. Ceribell complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Ceribell is an E-Verify employer. Any applicant with a disability who requires an accommodation during the application process should contact View email address on click.appcast.io to request reasonable accommodation.Privacy StatementFor information on how Ceribell processes personal data of job applicants, please review our Privacy Policy.Compliance DisclaimerIf you believe this job posting is non-compliant, please submit a report to View email address on click.appcast.io. Please note that we will not respond to inquiries unrelated to job posting compliance.
$370.04k
...covers. ️ About our Science Teams We are looking for a Principal Research Scientist to join the Multi-Embodiment Generalist Agent (MEGA) team... ...Yokohama, Herzliya, Vancouver and Leonberg. We operate a hybrid working model that combines in-person collaboration in our...SuggestedFull timeWork at officeRemote workVisa sponsorshipRelocation packageFlexible hoursShift work$32 - $36 per hour
...Hybrid Clinical Research Coordinator Pay Rate: $32-36/hr Employment Type: Contract Duration: 6 Months with possible extension... ...and respond to requests and questions. Collaborate with principal investigators and study sponsors, monitor and report serious...SuggestedFull timeContract workWork at officeMonday to Friday$148.1k - $192.5k
...planet. About the Role Seeking a talented RF MMIC Design researcher to drive cutting-edge MMIC innovation within Qorvo's Advanced Research... ..., phase shifters, attenuators, time-delay units (TDUs), hybrid multichip modules, or transmit/receive front-end modules (FEMs)...SuggestedFull timeWork at officeRelocation$70 - $80 per hour
Clinical Trial Manager W2 Contract-to-Hire Base Pay $70.00/hr - $80.00/hr Salary Range... ...0 per year Location Redwood City, CA - Hybrid Role Job Summary As a Clinical Trial Manager... ...in Clinical Operations or Clinical Research-related experience. Advanced knowledge...SuggestedContract workInterim role- ...reports to Manager, Medical Sciences and requires a strong candidate with expertise in the analysis of medical literature, data from clinical trials and pre-clinical studies, and sound knowledge of applicable regulations and standards. The position will mainly focus on...SuggestedLocal areaFlexible hours
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...employees to grow and develop their skills.The Clinical Scientist is involved in the design, monitoring,... ...States ideally the Scientist will work hybrid from our Palo Alto, CA office but we... ...with—and serve as a clinical research resource for—cross-functional colleagues...Full timeTemporary workWork at officeRemote workFlexible hours- ...reports to Manager, Medical Sciences and requires a strong candidate with expertise in the analysis of medical literature, data from clinical trials and pre-clinical studies, and sound knowledge of applicable regulations and standards. The position will mainly focus on...
$100k - $200k
...Senior Clinical Scientist Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of... ...management desirable. Experience working with external clinical research committees (i.e. screening committees, DSMB, CEC)....Work experience placementWorldwide$55 - $65 per hour
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$45 - $50 per hour
...Clinical Research Coordinator 1512819 ~ Hourly pay: $45-$50/hr ~ Worksite: Leading university (Palo Alto, CA 94304 - Hybrid) ~ W2 Employment, Group Medical, Dental, Vision, Life, Retirement... ...standards. Collaborate with principal investigators, sponsors, and research...Hourly payTemporary workWork at office$44.82 - $46.42 per hour
Job Title: Clinical Research Coordinator Duration: 06 Months Contract Location: Stanford, CA/Hybrid Pay Rate: $44.82- $46.42/hr Position Summary: Conduct clinical research and... ...requests and questions. Collaborate with principal investigators and study sponsors, monitor...Contract workWork at office$140k - $185k
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$346.64k
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...any discrepancies to a Senior, Reference, or Supervising Clinical Laboratory Scientist. Calibrates assays where the calibration is part of each... ...related to clinical issues, equipment or testing by initiating research utilizing available reference material. Reports and/or...Hourly payFull timeWork experience placementLocal areaShift work- ...Job Description Job Description AccuScan Sciences is seeking a California-licensed Clinical Genetic Molecular Biologist Scientist (CGMBS) to support and scale high-complexity molecular diagnostic testing within a CLIA-certified laboratory environment. This role is...
$65.9 - $84.97 per hour
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$20k
...companies working closely with CSBio to advance peptide-based clinical programs. Their work spans longevity and peptide therapeutics,... ...peptide facility and began producing high quality compounds for research organizations and pharmaceutical companies worldwide. In 2004,...Contract workImmediate startWorldwide2 days per week$22 - $25 per hour
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...Stanford University is seeking an Assistant Clinical Research Coordinator to perform administrative support duties related to the collection... ...of clinical studies. Work under supervision of the principal investigator and/or study coordinator/supervisor. Duties Include...Hourly pay
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