Scientific Writer - Integrative Oncology City of HopeScientific Writer - Integrative OncologyIrvine, CAYou will be responsible for producing high-quality, scientifically accurate, and engaging written content focused on Integrative Oncology, which combines mind-body practices, natural products, and lifestyle modifications with conventional treatments to support the Cherng Centers research, clinical, and educational initiatives. As a successful candidate, you will: • Write, edit, content style, and grammar/spelling, and proofread R01 and R01-like grant proposals, scientific manuscripts, for peer review, clinical study protocols, or other scientific documents for faculty research fellows and students.
NewScientific Writer - Orange County City of HopeScientific Writer - Orange CountyIrvine, CAAs a successful candidate, you will: Write, edit (content, style and grammar/spelling), and proofread¬ R01 and R01-like grant proposals, scientific manuscripts for peer review, INDs, clinical and IRB protocols, or other scientific documents for faculty, research fellows, and students. Join the forefront of groundbreaking research at the Beckman Research Institute of City of Hope, where we''re changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses.
Scientific Writer, Integrated Research Management Revolution Medicines IncScientific Writer, Integrated Research ManagementRedwood City, CA$143,000–$178,000 / 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 role partners closely with nonclinical subject matter experts (SMEs) in pharmacology, toxicology, and DMPK, as well as Regulatory Affairs, Regulatory Operations, and Medical Writers, to ensure nonclinical strategy and content are scientifically rigorous, aligned, and submission-ready.
Scientific Writer, Integrated Research Management Revolution MedicinesScientific Writer, Integrated Research ManagementRedwood City, CaliforniaThe 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 role partners closely with nonclinical subject matter experts (SMEs) in pharmacology, toxicology, and DMPK, as well as Regulatory Affairs, Regulatory Operations, and Medical Writers, to ensure nonclinical strategy and content are scientifically rigorous, aligned, and submission-ready.
Scientific Writer/Editor - ON-CALL ICF International IncScientific Writer/Editor - ON-CALLCA$61,232–$104,094 / yearPay Range - There are multiple factors that are considered in determining final pay for a position, including, but not limited to, relevant work experience, skills, certifications and competencies that align to the specified role, geographic location, education and certifications as well as contract provisions regarding labor categories that are specific to the position. We combine unmatched expertise with cutting-edge technology to help clients solve their most complex challenges, navigate change, and shape the future.
Scientific Writer / Project Development Scientist City of HopeScientific Writer / Project Development ScientistDuarte, CAThis is a unique hard-money position, where Dr. Erhunmwunsee seeks a research protégé who wishes to learn and grow under her mentorship the ideal candidate will advance in their career as the Lung, Justice, & Equity (LJE) lab and the Health Access and Community Enrichment office grows and succeeds. Lead end-to-end grant and scientific writing efforts, including identifying funding opportunities, developing and submitting proposals, managing deliverables, and representing the research program through publications, presentations, and external collaborations.
NewScientific Digital Content Writer (SEO & AI-Optimized Content) Thermo Fisher Scientific IncScientific Digital Content Writer (SEO & AI-Optimized Content)Carlsbad, CA$59,400–$99,000 / yearAs a Scientific Digital Content Writer, you will apply your scientific background and digital expertise to create clear, accurate, and high-performing content that supports our customers across the buyer journey. At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy.
Internal Communications and Science Writer UCLA Health SystemInternal Communications and Science WriterLos Angeles, CA$70,900–$145,200 / yearAs a condition of employment, the final candidate who accepts an offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; or have filed an appeal of a finding of substantiated misconduct with a previous employer. As the Internal Communications and Science Writer, you will create compelling content for both internal and external audiences, focusing on scientific research, advancements, and academic achievements.
Internal Communications and Science Writer University of CaliforniaInternal Communications and Science WriterLos Angeles, CA$70,900–$145,200 / yearAs a condition of employment, the final candidate who accepts an offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; or have filed an appeal of a finding of substantiated misconduct with a previous employer. As the Internal Communications and Science Writer, you will create compelling content for both internal and external audiences, focusing on scientific research, advancements, and academic achievements.
Medical Writer BioMarin Pharmaceutical IncMedical WriterSan Rafael, CA$74,100–$100,000 / yearntttttSearch JobsntttttntttttLocationntttttntttttSearch RadiusnttttttttttnttttttWithin 5 milesnttttttWithin 10 milesnttttttWithin 25 milesnttttttWithin 50 milesnttttttWithin 100 milesnttttttWithin 500 milesttttttntttttntttttntttttntttttntttt. nttttttDIN numbernttttttnttttttnttttttnttttt.
Senior Medical Writer BioMarin Pharmaceutical IncSenior Medical WriterCA$142,100–$195,360 / yearntttttSearch JobsntttttntttttLocationntttttntttttSearch RadiusnttttttttttnttttttWithin 5 milesnttttttWithin 10 milesnttttttWithin 25 milesnttttttWithin 50 milesnttttttWithin 100 milesnttttttWithin 500 milesttttttntttttntttttntttttntttttntttt. nttttttDIN numbernttttttnttttttnttttttnttttt.
NewSenior Medical Content Writer, Claims-Capable Pride GlobalSenior Medical Content Writer, Claims-CapableSouth San Francisco, CA$50–$68.68 / hourOnly applicable for San Francisco Candidates: Under the San Francisco Lactation in the Workplace Ordinance, we will provide written notice of lactation accommodation rights, and this notice will automatically be given upon hiring, upon any inquiry of parental leave or lactation accommodation. This role focuses on creating and substantiating medical claims, producing MLR-ready content, and collaborating with creative, medical, and regulatory teams to deliver accurate, compliant, and engaging materials.
Medical Writer II Allen SpoldenMedical Writer IICalifornia City, CaliforniaManages the document development process from start to finish which may include generating multiple draft documents and formulating final approved versions, editing, reference retrieval, as well as managing other various processes are undergone (i.e., internal & external reviews, quality checks, audits, formatting, publishing). Participates in all necessary cross-functional document development meetings (i.e., kick-off meetings, comment resolution meetings) to ensure appropriate alignment from different stakeholders.
NewSenior Medical Content Writer, Claims-Capable HireTalentSenior Medical Content Writer, Claims-CapableSouth San Francisco, CAYou will work embedded in an in-house creative studio, alongside creative directors and designers, which means your writing needs to work as creative material, not just as reference text. You will develop, substantiate, and annotate promotional and educational claims, and write the medical content that carries them accurately, clearly, and in a way that survives MLR review without losing its edge.
Technical Writer - Product Development (Dental Devices) Glidewell DentalTechnical Writer - Product Development (Dental Devices)Irvine, CaliforniaEssential Functions : Collaborates with Research & Development, Manufacturing and Marketing teams to accurately document test methods, technical reports, labels, and other design file documents for specific market products. From SOPs and test methods to IFUs and technical reports, you’ll play a key role in making sure our products are accurately documented and ready for market.
Technical Documentation Writer Takara Bio USA IncTechnical Documentation WriterSan Jose, CA$105,000–$115,000 / yearHow this role drives the company forward: A Technical Documentation Writer is responsible for producing product-related technical documents (e.g., user manuals, protocols, certificates of analysis, technical notes, scientific posters, and manuscripts) that are clear, logical, and follow the company style guide. A Technical Documentation Writer demonstrates strong writing skills and works independently for most tasks, consulting with more senior members of the Technical Communications team to receive guidance on challenging projects.
Senior Medical Writer Argenx SESenior Medical WriterCA$128,000–$176,000 / yearargenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by VYVGART, our first-in-class neonatal Fc receptor blocker approved for the treatment of gMG, and with the potential to treat patients across dozens of severe autoimmune diseases. For the expansion of our team, argenx is looking for a Senior Medical Writer who will provide medical writing support for developing complex clinical, nonclinical, and safety documents for regulatory submissions.
Scientific Communications - Social Media & Community Management Zymo Research CorporationScientific Communications - Social Media & Community ManagementTustin, CA$75,000–$90,000Recognized as a Top Workplace by the Orange County Register in 2021, 2022, and named a Top Workplace USA in 2023, Zymo Research continues to be a vibrant community where employees thrive, feel connected, and are inspired by their work. This role will translate product stories, brand initiatives, scientific resources, programs, events, and community opportunities into social content that feels credible, useful, visually engaging, and relevant to researchers.
Associate Regulatory (Medical Writing) Scientific Communications Director Exelixis IncAssociate Regulatory (Medical Writing) Scientific Communications DirectorAlameda, CA$148,500–$209,500 / yearEducation: BS/BA degree in related discipline and a minimum of eleven years of related experience including industry; or, MS/MA degree in related discipline and a minimum of nine years of related experience including industry; or, PhD in related discipline and a minimum of five years of related experience including industry; or Equivalent combination of education and experience. Incorporates diverse reviewer feedback while ensuring high quality of content organization, including completeness, clarity, coherence, conciseness, consistency, and accuracy.
NewSenior Medical Content Writer, Claims-Capable Actalent IncSenior Medical Content Writer, Claims-CapableSouth San Francisco, CA$41–$64 / hourWe are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. Write medical content across various formats, including HCP materials, patient education, disease-state content, congress panels, digital assets, video scripts, and sales materials.
Quality Technical Writer Actalent IncQuality Technical WriterIrvine, CA$40–$50 / hourWe are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. The candidate will be helping the team by predominantly investigating non-conformances and deviations, writing technical reports and will work in one of their contained facility labs.
Quality Technical Writer -NCs And CAPA's Actalent IncQuality Technical Writer -NCs And CAPA'sIrvine, CAHeadquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC-with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering.
Executive Director, Scientific Publications (Oncology) Exelixis IncExecutive Director, Scientific Publications (Oncology)Alameda, CA$273,000–$388,000 / yearResponsibilities include management of the Publications team, oversight of publication planning for each Exelixis development compound, coordination of publication planning and tactical execution with cross-functional collaborators, contribution to publication project execution as needed, management of publication vendors and responsibility for compliance aspects of the publication function. EDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS: Education/Experience: Doctorate level degree (PharmD, MD, PhD) with a minimum of 15 years of related experience; or, Master's level degree in related discipline and a minimum of 16 years of related experience; or, Bachelor's level degree in related discipline and a minimum of 18 years of related experience; or, Equivalent combination of education and experience.
Medical Writer / Medical Reviewer Consultant - Oncology Ovarian Cancer ClinChoice IncMedical Writer / Medical Reviewer Consultant - Oncology Ovarian CancerCARemoteThe successful candidate will collaborate with Medical Affairs, Clinical Development, Regulatory Affairs, Biostatistics, and external experts to ensure scientific accuracy, compliance, and timely execution of deliverables. We are seeking an experienced Medical Writer or Medical Reviewer with expertise in Ovarian Cancer and Gynecologic Oncology to support the development, review, and delivery of high-quality scientific and medical content.
Technical Documentation Writer Takara Bio—HomeTechnical Documentation WriterSan Jose, CaliforniaA Technical Documentation Writer is responsible for producing product-related technical documents (e.g., user manuals, protocols, certificates of analysis, technical notes, scientific posters, and manuscripts) that are clear, logical, and follow the company style guide. A Technical Documentation Writer demonstrates strong writing skills and works independently for most tasks, consulting with more senior members of the Technical Communications team to receive guidance on challenging projects.
Medical Writer CollateMedical WriterSan Francisco, CaliforniaThe base salary range for this role is competitive, depending on experience and level (Tier 1, San Francisco) We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. Serve as a pharma insider resource — helping us understand org structures, roles, timelines, and internal processes at target pharma companies, and weighing in on industry relationships and positioning (e.g., which pharma leaders and functions we should be building relationships with).
Senior Director/Executive Director, Scientific Communications Coherus Oncology IncSenior Director/Executive Director, Scientific CommunicationsRedwood City, CA$230,000–$290,000 / yearThis highly visible role will partner closely with Medical Affairs, Clinical Development, Translational Medicine, Biostatistics, Regulatory Affairs, Legal, Compliance, Commercial, and Executive Leadership to develop and maintain a compelling scientific narrative across all stages of product development. The Senior Director/Executive Director will lead publication strategy and execution, scientific platform development, congress communications, and field medical content development while ensuring alignment with broader Medical Affairs, Clinical Development, and corporate objectives.
Principal Regulatory Writer (Temporary) Vir BiotechnologyPrincipal Regulatory Writer (Temporary)San Francisco, CARemote$180–$200 / hourManage medical writing projects, including developing timelines (working with the study/project teams, as necessary) and communication with cross-functional team members to maintain awareness of review cycles and expectations. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple PRO-XTEN ® dual-masked T-cell engagers across validated targets in solid tumor indications.
Senior Regulatory Writer (Temporary) Vir BiotechnologySenior Regulatory Writer (Temporary)San Francisco, CARemote$130–$170 / hourIts clinical-stage portfolio includes programs for chronic hepatitis delta and multiple PRO-XTEN ® dual-masked T-cell engagers across validated targets in solid tumor indications. Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer.
Regulatory Writer and/or Regulatory QC/ Editor Vir BiotechnologyRegulatory Writer and/or Regulatory QC/ EditorSan Francisco, CARemote$90–$120 / hourVir Biotechnology is looking for a Regulatory Writer (Temporary) who will support the quality, consistency, and accuracy of regulatory documents produced by the Regulatory Writing team by either functioning as a support author and/or by focusing on editorial and QC review of documents written by other team members. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple PRO-XTEN ® dual-masked T-cell engagers across validated targets in solid tumor indications.
Senior Technical Writer—Needed---Local to Bay area California Needed DELTASOFT SOLUTIONS LLCSenior Technical Writer—Needed---Local to Bay area California NeededSan fransico, CAWorking independently, the demonstrates advanced knowledge and technical competence in a senior professional level role, and applies advanced technical skills to multiple, complex projects as a subject matter expert and project leader across departments. Data Management: Gathers, groups, classifies, or arranges written information or data in some meaningful order or form (e.g., reports, charts, graphs); data management includes determining what data to gather; and accurately maintaining data files.
Clinical Medical Writer Consultant KaztronixClinical Medical Writer ConsultantSan Diego, CARemoteThis role requires close partnership with Clinical Development, Clinical Operations, Biostatistics, Data Management, Regulatory Affairs, Pharmacovigilance, and external vendors to ensure timely delivery of accurate, scientifically rigorous documents. This individual will play a key role in advancing multiple late-stage clinical programs, with primary responsibility for authoring and coordinating clinical study documentation for Phase 2 and Phase 3 trials.
Associate Director, Regulatory and Medical Writer Ionis Pharmaceuticals IncAssociate Director, Regulatory and Medical WriterCarlsbad, CARemote$142,588–$201,472 / yearRESPONSIBILITIES: Working with the Executive Director, Regulatory and Medical Writing, lead the development, authoring, and delivery of complex regulatory documents such as clinical study reports and marketing application summary documents (Module 2), and lead and/or contribute to Investigator's Brochures, clinical study protocols, and briefing documents. With multiple marketed medicines and a leading pipeline in neurology, cardiology and select areas of high patient needs, we continue to drive innovation in RNA therapies in addition to advancing new approaches in gene editing to provide greater value to patients and are well positioned financially to deliver on our strategic goals.
Technical Writer Argonaut Manufacturing Services IncTechnical WriterCarlsbad, CA$105,000–$115,000 / yearArgonaut Manufacturing Services Inc. is a contract manufacturing organization (CMO) headquartered in Carlsbad, CA with over 100,000 square feet of manufacturing space across four locations. This role is responsible for leading high-quality cGMP investigations, driving root cause elimination, and implementing sustainable corrective and preventative actions (CAPAs).
Technical Writer (Part-time or Full-time) [Closed] System Biosciences LLCTechnical Writer (Part-time or Full-time) [Closed]Santa Clara, CADescription: We are looking for an experienced Technical Writer to prepare technical manuals, promotional materials, and web site contents related to life science research reagents. Have some experience in preparing brochures, catalogues, protocols, and user manuals in life science industry.
NewClinical Medical Writer Integrated Resources, IncClinical Medical WriterCaliforniaContractorUnderstand relationships and dependencies between documents and analyses produced for regulators including the development RMP, DSUR, PBRER, and ACO.• Collaborate with quality lines and relevant project team subject matter experts, ensuring the accuracy and quality of information presented in assigned documents.• Qualifications• Degree or qualification in life sciences (e.g., MD, DVM, PhD in relevant field, BSN, PharmD, Master's or Bachelors' degree in relevant field); alternatively, bachelor's or higher degree in field with transferable skills and pharmaceutical industry experience, ideally in safety, regulatory or clinical areas.•
Technical Writer III, YouTube Developer Infrastructure Google LLCTechnical Writer III, YouTube Developer InfrastructureSan Bruno, CAIn this role, you'll have the independence to lead complex technical documentation projects, working directly with subject matter experts from YouTube infrastructure teams to document core tech stacks and developer APIs for both internal and external engineering partners. You will support infrastructure teams across YouTube, researching and creating documentation for the tools, frameworks, and platforms that power the world's most popular video destination.
Senior Regulatory Medical Writer Ionis Pharmaceuticals IncSenior Regulatory Medical WriterCarlsbad, CARemote$113,000–$142,426 / yearThis role includes responsibilities throughout the lifecycle of a document including working cross-functionally to interpret source information (including leading data interpretation meetings), leading key messaging meetings, writing content following US and international regulations (including Marketing Application Module 2 summary documents), conducting quality control (QC) reviews, resolving Quality Assurance (QA) audit findings, and working with Regulatory Operations for publishing and submission. Experience writing, as lead and/or contributor, important regulatory and clinical documents such as clinical study reports (all sections including safety narratives), Investigator's Brochures, clinical study protocols, drug marketing application summary documents, Investigational New Drug applications, clinical sections of New Drug Applications, and other regulatory documents (e.g., Briefing Documents) for submission.
Proposal & Report Writer Critical InnovationsProposal & Report WriterLawndale, CA$50,000–$75,000 / yearThis includes preparing and submitting contract reports, monitoring deadlines for contract deliverables, and assisting with preparation of additional written materials (e.g., slide decks, poster presentations, publications, proposals). The Proposal and Report Writer works closely with and under the supervision of the Grants & Contracts Coordinator I to complete writing related tasks in the following categories: Contract report writing .
Technical Writer (onsite) MKS2 TechnologiesTechnical Writer (onsite)Monterey, CA$65,000–$78,000 / yearMKS2 Technologies, LLC, an award-winning high growth small business, creates innovative and customer-centric technology solutions in the areas of Cyber Security, Instructional Design and Training, Software Engineering and IT Support Services to improve the security and well-being of our clients. Demonstrated ability to independently research, write, and edit materials such as white papers, fact sheets, multimedia content, web features, press releases, and newsletter articles.
Associate Director, Medical Writer MannKind CorpAssociate Director, Medical WriterWestlake Village, CARemoteMannKind Corporation is a biopharmaceutical company dedicated to transforming chronic disease care through innovative, patient‑centric solutions, developing and commercializing innovative inhaled therapeutics and drug‑device technologies aimed at addressing serious unmet needs across endocrine, cardiorenal, and orphan lung diseases. Oversee the development and finalization of high-quality, scientifically accurate, ICH-compliant documents, including clinical study protocols and reports, Investigator Brochures, Periodic Safety Updates, patient narratives, and manuscripts for peer-reviewed publications.
NewBatch Record Writer Fladger AssociatesBatch Record WriterFremont, CAWrites, and edits technical documents related to bio-manufacturing by working seamlessly with cross functional teams under general supervision. Batch record flow should be consistent across different products and learnings from a particular campaign should be carried forward to the next set of batch records.
NewSr.Medical Writer Integrated Resources, IncSr.Medical WriterCaliforniaContractorEach document will be prepared according to the project team specified timelines, and such timelines will be clearly communicated to the Contractor FTE.Phase 2 - Document Development• After agreement of the document strategy between team and the Contractor FTE, the POC will communicate with the Contractor FTE regularly, or as needed, to discuss progress (the Contractor FTE should not wait for a scheduled meeting in order to resolve issues that prevent progress)• More urgent jobs may require daily meetings in order to meet project timelines• The Contractor FTE may coordinate and lead meetings (e.g., regularly scheduled team meetings, immersion meetings to review comments, etc.)• Documents should be prepared and maintained in Global Document Management System (GDMS) at all times to enable real time review of the current draft.• Job DescriptionThe Contractor will work in three phases:Phase 1 – Document Initiation• At initiation of a new deliverable, the relevant Therapeutic Area (TA) authoring team will provide the Contractor FTE with all relevant information required to complete the deliverables, including a description of the required activities, names of colleagues who will be providing input, timelines, the names of reviewers and approvers and the final handover customer.•
NewTechnical Writer TechDigitalTechnical WriterSan Jose/Mountain View, CAHardware Documentation: Produce clear, visual-heavy guides for the setup, calibration, hygiene, and maintenance of proprietary AR headsets, sensors, and motion. Video Production: Ability to film and edit short instructional videos (Premiere Pro, Camtasia) for training purposes.
Clinical Research Program Manager - Quality Outcome & Grant Writing Pacific Neuropsychiatric SpecialistsClinical Research Program Manager - Quality Outcome & Grant WritingIrvine, CaliforniaThis position will work directly with the clinicians and data analysts to establish research infrastructure, manage regulatory processes, coordinate clinical outcomes research, and assist in preparing manuscripts and scholarly publications in mental health and substance use clinical care. This role does not require independent grant writing or serving as a principal investigator but requires the ability to translate research concepts into well-organized protocols and publication-ready manuscript drafts and grants.
NewSenior Copywriter Syneos - Commercial - ProdSenior CopywriterSanta Monica, CA$100,000–$110,000 / yearYou’ll partner closely with art directors on brand and concept development, provide support to ACDs and CDs within the Core Brand Team, and play a hands-on role in bringing smart, compelling ideas to life. You are both a thinker and a doer—equally comfortable crafting breakthrough concepts, writing sharp copy across channels (including social), and confidently presenting ideas internally and to clients.
Social Media & Community Manager - Life Sciences Zymo Research CorporationSocial Media & Community Manager - Life SciencesTustin, CA$75,000–$90,000Recognized as a Top Workplace by the Orange County Register in 2021, 2022, and named a Top Workplace USA in 2023, Zymo Research continues to be a vibrant community where employees thrive, feel connected, and are inspired by their work. This role will translate product stories, brand initiatives, scientific resources, programs, events, and community opportunities into social content that feels credible, useful, visually engaging, and relevant to researchers.
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.
AI research scientist WriterAI research scientistSan Francisco, CaliforniaThe instincts and orientation that match WRITER's values: you Connect — you collaborate openly across research, engineering, and product and communicate complex ideas with clarity to both technical and non-technical audiences; you Challenge — you ask the hard questions, push back on conventional wisdom, and pursue the research directions others haven't tried yet; you Own — you drive your projects end-to-end with urgency, take accountability for results, and care deeply about the impact your work has on real customers. Founded in 2020 with office hubs in San Francisco, New York City, Austin, Chicago, and London, our team thinks big and moves fast, and we're looking for smart, hardworking builders and scalers to join us on our journey to create a better future of work with AI.
Staff AI research scientist Writer IncStaff AI research scientistSan Francisco, CAThe instincts and orientation that match WRITERs values: you Connect - you collaborate openly across research, engineering, and product and communicate complex ideas with clarity to both technical and non-technical audiences; you Challenge - you ask the hard questions, push back on conventional wisdom, and pursue the research directions others havent tried yet; you Own - you drive your projects end-to-end with urgency, take accountability for results, and care deeply about the impact your work has on real customers. Founded in 2020 with office hubs in San Francisco, New York City, Austin, Chicago, and London, our team thinks big and moves fast, and were looking for smart, hardworking builders and scalers to join us on our journey to create a better future of work with AI.