Medical Writer - Clinical Regulatory Documentation Perspective TherapeuticsMedical Writer - Clinical Regulatory DocumentationUnited StatesFull timeReporting to the Head of Medical/Regulatory Writing, the Medical Writer – Clinical Regulatory Documentation will be responsible for the preparation and delivery of high-quality, scientifically accurate, and regulatory-compliant clinical/medical documentation to support clinical development and regulatory submissions. Project Support: Provide medical writing support across various stages of clinical development, including early-phase studies, late-stage clinical trials, and regulatory submissions.
Medical Writer - Scientific Communications Perspective TherapeuticsMedical Writer - Scientific CommunicationsUnited StatesFull timeProject Support: Provide medical writing support across various stages of clinical development, including early-phase studies, late-stage clinical trials, and nonclinical and CMC teams as needed. Cross-Functional Collaboration: Work closely with clinical development, regulatory affairs, and other stakeholders (e.g., nonclinical, CMC etc) to ensure that all medical writing deliverables meet project objectives, timelines, and internal and external requirements.
Medical Writer - India (56829) Praxis Precision MedicinesMedical Writer - India (56829)Boston, MACollaborates with cross-functional team members, eg, Clinical Pharmacology, Toxicology, Research, Clinical Development, Regulatory Affairs, Biostats, Data Management, Quality, CMC, QC, etc., to ensure accurate and timely completion and delivery of high-quality, scientifically-sound documents, slide decks, and publications. This requires the knowledge and expertise to collaboratively author required documents with support and input from the Associate Director, Medical Writing while also helping other teams follow medical writing processes and style requirements.
Senior Medical Writer LumanitySenior Medical WriterYardley, PennsylvaniaRemoteResponsibilities / Position overview: We are seeking an advanced degree life-sciences professional to serve as a Senior Medical Writer within our Medical Strategy and Communications team, which serves our clients by mobilizing our scientific knowledge to interpret the data and create compelling narratives to guide their medical strategy and through regulatory challenges. The Senior Medical Writer will ensure high-quality content is developed for a wide range of medical communications projects and deliverables including clinical publications (manuscripts and abstracts), slide decks, scientific platforms, symposia, advisory boards, and training materials.
Associate Medical Writer MJH Life SciencesAssociate Medical WriterCranbury, New JerseyThe Associate Medical Writer at Pharmacy Times Continuing Education (PTCE) plays a vital role in supporting the Scientific Affairs and Business Development teams by contributing to the development of CE-certified educational content. Ability to interpret complex clinical data and outcomes reports to identify learning trends and educational needs.
Medical Writer SystImmune, Inc.Medical WriterPrinceton, NJ$80,000–$130,000 / yearThe medical writer will be responsible for the management and oversight of assigned medical writing projects, including clinical study protocols and reports, investigational new drug applications (INDs), investigator brochures, reviewing informed consent forms and regulatory briefing materials. Write, edit and/or manage the production of high-quality clinical documentation including clinical study protocols, synopses, and clinical study reports for submission to regulatory authorities in support of marketing applications and BLAs.
NewMarket Access Medical Writer GLE Creative TalentMarket Access Medical WriterNew YorkRemote$100,000–$160,000 / yearWorking closely with internal teams and clients, youll translate complex clinical data into clear, compelling narratives that support payer engagement and brand success. As a Medical Writer, Market Access , you will play a critical role in developing strategic, scientifically accurate content that drives brand differentiation and maximizes access goals.
Medical Writer MJH Life SciencesMedical WriterRemoteIn this role, you’ll translate complex clinical data into clear, compelling deliverables across multiple formats, such as articles, white papers, slide decks, digital media, and live event content. The Medical Writer plays a critical role in creating accurate, engaging, and compliant scientific content for a variety of audiences, including healthcare professionals, patients, and industry stakeholders.
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.
Medical Writer Systimmune IncMedical WriterPrinceton, NJ$80,000–$130,000 / yearPosition Summary: The medical writer will be responsible for the management and oversight of assigned medical writing projects, including clinical study protocols and reports, investigational new drug applications (INDs), investigator brochures, reviewing informed consent forms and regulatory briefing materials. Key Responsibilities: Write, edit and/or manage the production of high-quality clinical documentation including clinical study protocols, synopses, and clinical study reports for submission to regulatory authorities in support of marketing applications and BLAs.
Senior Medical Writer OSI PharmaceuticalsSenior Medical WriterBoulder, ColoradoWorks with clinical, data management and biostatistics staff to develop report formats and write final drafts of clinical study reports. May draft manuscripts, Investigator’s brochures, Annual Reports, Protocols and package insert materials or promotional materials, as needed by individual project teams in Clinical Development.
Medical Writer BioMarin PharmaceuticalMedical WriterSan Rafael, CaliforniaFilling this need with a regular full-time employee will enable BioMarin to reduce writing-related CRO and contractor costs, increase Medical Writing productivity to meet development needs, and realize efficiencies and consistent documentation quality across programs through repeatable processes and continuity of knowledge of programs, investigational products, and indications. ·Basic applied knowledge of: odocumentation required for the conduct of clinical studies oprotocol design (including objectives, efficacy and safety endpoints, and procedures for collecting and reporting AEs and SAEs) ostudy results reporting Medical Writing ·Writing high-quality documents that support corporate goals and objectives.
Associate Director, Medical Writer Celldex Therapeutics IncAssociate Director, Medical WriterNew Haven, CT$153,616–$199,501 / yearResponsible for the generation of clinical regulatory documents including, but not limited to: briefing documents, IND annual reports, Investigator''s Brochures, clinical protocols and amendments, clinical study reports, scientific manuscripts and abstracts. The Associate Director, Medical Writer at Celldex will lead the development and management of complex clinical and regulatory documents, including protocols, investigator brochures, study reports, and regulatory submissions for our immunology programs.
Senior Medical Writer fingerpaintSenior Medical WriterObjectives of This Role: A Senior Medical Writer is responsible for the planning, preparation, development, and/or review of scientific/medical content in a variety of formats (slides, newsletters, storyboards, etc.); accurate interpretation of data; clear communication with clients, speakers, and HCPs; efficient planning and organization; establishing effective working interactions with account services, editorial, creative, and project management teams; and efficiently producing high-quality deliverables. Fingerpaint Group’s medical communications solutions, Fingerpaint Medical, help pharmaceutical and biotech companies communicate complex scientific data effectively, enabling healthcare providers to make informed decisions that advance patient care.
Medical Writer PhD Cardiovascular/Metabolic Cincinnati Medpace Holdings IncMedical Writer PhD Cardiovascular/Metabolic CincinnatiCincinnati, OHPhD in Life Sciences with a focus in Cardiovascular and/or Metabolic research (clinical or nonclinical);• Ability to synthesize complex information into a clear and concise format that is appropriate for the target audience;• Energetic and enthusiastic team-player that is self-motivated and eager to learn and grow in the position; and• Prior experience in the CRO, pharmaceutical, or medical writing industries is not required but is advantageous. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Medical Writer PhD Hematology/Oncology Cincinnati Medpace Holdings IncMedical Writer PhD Hematology/Oncology CincinnatiCincinnati, OHPhD in Life Sciences with a focus in Hematology and/or Oncology research (clinical or nonclinical);• Ability to synthesize complex information into a clear and concise format that is appropriate for the target audience;• Energetic and enthusiastic team-player that is self-motivated and eager to learn and grow in the position; and• Prior experience in the CRO, pharmaceutical, or medical writing industries is not required but is advantageous. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Senior Regulatory Medical Writer - Fractional (Remote) Penfield Search PartnersSenior Regulatory Medical Writer - Fractional (Remote)Fairfield, CTRemoteSupport preparation and maintenance of protocol amendments, submission support documents, and related deliverables within Common Technical Document (CTD Modules 2–5) across the submission lifecycle (responses, amendments, briefing packages). This role focuses on independently updating and finalizing regulatory documents to support ongoing agency interactions and submission deliverables, working alongside internal and contract writers.
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).
NewSr Medical Writer IRESr Medical WriterKey responsibilities include: Leading the preparation, review, and editing of clinical study documents, including clinical study protocols, clinical study reports (CSRs), investigator brochures (IBs), and regulatory submissions, ensuring accuracy, clarity. Collaborating closely with cross-functional teams, including clinical research, biostatistics, regulatory affairs, and medical affairs, to interpret and analyze clinical trial data, summarize scientific findings.
Contract Medical Writer (Scientific Communications) MJH Life SciencesContract Medical Writer (Scientific Communications)RemoteThis role partners with Medical Affairs and account teams to create advisory board content, training resources, and scientific messaging that supports healthcare professionals across live, digital, and field-facing channels. We are seeking a Contract Medical Writer (Scientific Communications) to support the development of high-quality, evidence-based medical communications materials.
Assistant Medical Writer - Hybrid Role AdMed Inc.Assistant Medical Writer - Hybrid RolePhiladelphia, PAAdMed is an award winning, integrated agency that designs and delivers modern training tools for pharmaceutical, biotech, diagnostic and medical products, with one goal: to ensure that healthcare professionals, sales teams, employees and consumers understand what they need to know regarding the science behind their products. AdMed has over 30 years of industry experience and we are looking for a dynamic, passionate, experienced Assistant Medical Writer to join our team.
Senior Medical Writer St. Jude Children's Research Hospital IncSenior Medical WriterMemphis, TN$78,000–$139,360 / yearThis role serves not only as a key contributor to content development but also as a central project facilitator-driving cross-functional alignment, ensuring timely execution, and coordinating activities across stakeholders to support successful delivery of clinical and CMC documentation for clinical programs. CMC Medical Writer is responsible for providing clinical, scientific, technical writing, and project coordination expertise for essential clinical and chemistry, manufacturing, and controls (CMC) documents submitted to the FDA and other regulatory agencies to support St.
Medical Writer - PhD - Cardiovascular/Metabolic - Cincinnati Medpace, Inc.Medical Writer - PhD - Cardiovascular/Metabolic - CincinnatiCincinnati, OhioQualifications: • PhD in Life Sciences with a focus in Cardiovascular and/or Metabolic research (clinical or nonclinical); • Ability to synthesize complex information into a clear and concise format that is appropriate for the target audience; • Energetic and enthusiastic team-player that is self-motivated and eager to learn and grow in the position; and. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Medical Writer - PhD - Hematology/Oncology - Cincinnati Medpace, Inc.Medical Writer - PhD - Hematology/Oncology - CincinnatiCincinnati, OhioQualifications: • PhD in Life Sciences with a focus in Hematology and/or Oncology research (clinical or nonclinical); • Ability to synthesize complex information into a clear and concise format that is appropriate for the target audience; • Energetic and enthusiastic team-player that is self-motivated and eager to learn and grow in the position; and. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Senior Medical Writer Health InteractionsSenior Medical WriterYardley, PADrawn together from several backgrounds including the pharmaceutical industry, research, marketing, medical and regulatory writing, sales, publishing, digital media and design, we have the experience and all-round ability to conceive and deliver the best quality medical communications programs. We consider compensation more than just a base salary - that's why we also offer an exceptional range of flexible benefits, personal support and tailored learning and development opportunities all designed to help you realize your full potential both in life and at work.
Senior Medical Writer Centessa Pharmaceuticals PlcSenior Medical WriterBoston, MA$150,000–$190,000 / yearOversee document preparation from start to finish, including kick-off activities and planning, drafting, managing review cycles, incorporating feedback and revisions, addressing quality control and quality assurance findings, and providing a final version within document timelines. Strong organizational, communication, and influencing skills; ability to prioritize, multitask, and deliver high-quality documents under tight timelines.
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.
Associate Medical Writer MJH Life Sciences Multimedia Medical LLCAssociate Medical WriterCranbury, NJ$65,000–$75,000 / yearThe Associate Medical Writer at Pharmacy Times Continuing Education (PTCE) plays a vital role in supporting the Scientific Affairs and Business Development teams by contributing to the development of CE-certified educational content. Ability to interpret complex clinical data and outcomes reports to identify learning trends and educational needs.
Senior Medical Writer (Fixed-Term Contract) COMPASS Pathways PlcSenior Medical Writer (Fixed-Term Contract)New York, NY$135,000–$185,000 / yearCOMP360 has Breakthrough Therapy designation from the US Food and Drug Administration (FDA) and has received Innovative Licensing and Access Pathway (ILAP) designation in the UK for treatment-resistant depression (TRD) due to the pressing unmet need in this area. We are currently in phase 3 for TRD, have completed phase 2 studies for both post-traumatic stress disorder (PTSD) and anorexia nervosa and are planning a further late-stage study in PTSD.
Experienced medical writer – USA AmiculumExperienced medical writer – USAChicago, IllinoisAs a result of this success, Amiculum is looking for an experienced medical writer with a passion for publications who enjoys building positive long-term relationships, identifying opportunities, and helping to drive organic growth. Providing clients with a high level of scientific expertise on medical communications projects, with a focus on publications, including abstracts, posters and manuscripts.
NewSenior Medical Writer BGBxSenior Medical Writer$90,000–$115,000 / yearWe're looking for individuals who would enjoy working on a range of projects, including traditional "left-brained" projects (complex scientific analysis) and traditional "right-brained" projects (creative, innovative communications). Our teams work across consulting and communications to help clients shape strategy, launch innovations, engage stakeholders, and drive meaningful results throughout the product lifecycle.
Principal Medical Writer ICON PlcPrincipal Medical WriterBlue Bell, PAAs a Principal Medical Writer at ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical information. Collaborating with cross-functional teams, including clinical research, biostatistics, and regulatory affairs, to gather and synthesize information for document development.
Medical Writer Perceptive Informatics LLCMedical WriterMA$65,305–$93,000 / yearThe Medical Writer will create, research, edit and coordinate the production of clinical documents related to independent review, including independent review charters, clinical data forms, manual case report forms, applicable reviewer training materials, project deviations and supplementary imaging reports, using available central content and templates. Serve as the medical writing representative on assigned project teams communicate content requirements, Coordinate and conduct interdepartmental team reviews of draft and final documents, Evaluate progress on tasks, identify issues and facilitate resolutions, and advance document development to approval, according to Calyx and/or client guidelines/SOPs.
Medical Writer Nucleus Global LtdMedical WriterYardley, PARegardless of past practice, all resumes submitted by search firms to any employee of Nucleus Global and its affiliated companies via email, the Internet or in any form - without a current signed fee agreement for that position (as authorized by the Recruitment Manager) - will be deemed the sole property of Nucleus Global, and no fee will be paid in the event the candidate is hired as a result of the referral or through other means. You will be required to participate in client meetings / teleconferences and attend scientific meetings such as congress, symposia and advisory boards and participate in pre-meetings, onsite activities and post meeting work as required / appropriate.
Medical Writer Health InteractionsMedical WriterYardley, PARegardless of past practice, all resumes submitted by search firms to any employee of Nucleus Global and its affiliated companies via email, the Internet or in any form - without a current signed fee agreement for that position (as authorized by the Recruitment Manager) - will be deemed the sole property of Nucleus Global, and no fee will be paid in the event the candidate is hired as a result of the referral or through other means. You will be required to participate in client meetings / teleconferences and attend scientific meetings such as congress, symposia and advisory boards and participate in pre-meetings, onsite activities and post meeting work as required / appropriate.
Senior Medical Writer MedtronicSenior Medical WriterNorth Haven, ConnecticutRemoteThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
NewSr. / Principal Medical Writer (Regulatory focus) - Sponsor-dedicated; NA/CAN/UK Syneos Health IncSr. / Principal Medical Writer (Regulatory focus) - Sponsor-dedicated; NA/CAN/UKINTogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
NewSr. Medical Writer (Regulatory) Syneos Health IncSr. Medical Writer (Regulatory)MDTogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
NewPrincipal Medical Writer - Publications Syneos Health IncPrincipal Medical Writer - PublicationsPATogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
NewSr Medical Writer - Late Phase - Inflammation Syneos Health IncSr Medical Writer - Late Phase - InflammationNCTogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
Medical Writer Position Integrated Resources, IncMedical Writer PositionGroton, ConnecticutContractorHighly organized, ability to prepare technical reports, summaries, protocols, and quantitative analysesTechnical Knowledge:Able to work well in cross-functional teams, exhibiting a combination of active listening skills and also the confidence to guide decision-making for the document content strategy. Job DescriptionResponsibilities:Prepare the Clinical Overview, integrated safety, efficacy, pharmacology and bio therapeutic summaries, regulatory responses, internal and external risk/benefit briefing documents, for one or more assigned products.
Medical Writer Knowesis, Inc.Medical WriterEast Orange, NJ$85,000–$89,000 / yearDevelop, write, and edit a wide range of clinical, scientific, and research-based documents, including study protocols, leadership reports, manuscripts for publication, regulatory submissions, grant proposals, and other technical materials essential to research and clinical operations. Maintain up-to-date VHA-required training for all personnel involved in patient care and/or research studies, including but not limited to: VA Privacy and Information Security Awareness and Rules of Behavior; VHA Privacy Policy Web Training; and Collaborative Institutional Training Initiative (CITI) Program Training.
Principal Medical Writer MJH Healthcare Holdings LLCPrincipal Medical WriterRemote$95,000–$105,000 / yearYou actively use tools such as ChatGPT, Claude, or AI-assisted research and writing platforms to improve how you work and can clearly articulate how they enhance output quality and efficiency - while maintaining scientific integrity and compliance. Provide mentorship, training, and editorial guidance to junior Medical Writers and Editors, supporting their development and helping the team consistently deliver high-quality work.
Principal Medical Writer ProPharma GroupPrincipal Medical WriterRaleigh, North CarolinaWith deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies.
Principal Medical Writer, Cardio/Metabolic Health ProPharma GroupPrincipal Medical Writer, Cardio/Metabolic HealthChicago, IllinoisWith deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies.
Medical Writers Integrated Resources, IncMedical WritersLower Gwynedd Township, PennsylvaniaContractorMedical WritersA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. Looking for Medical Writers in Springhouse, PAClient -Johnson and JohnsonPlease share the updated resume at sweta(at)irionline.com
Medical Writer, Scientific Intelligence Vaniam GroupMedical Writer, Scientific IntelligenceRemoteA Day in the Life Deliverables Develop high-quality content for an array of projects, including publications (eg, abstracts, presentations, and manuscripts), advisory boards, scientific platforms, gap analyses, literature summaries, slide sets, and training materials. Actively contribute to the ongoing improvement of Vaniam Group’s LLM by applying and sharing deep scientific and therapeutic area expertise to inform, validate, and refine AI outputs.
Senior Medical Writer (Remote) MMSSenior Medical Writer (Remote)Boston, MARemoteFull timeWrite and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 documents, presentation materials and publications to medical journals. Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide.
Medical Writer MJH Life Sciences Multimedia Medical LLCMedical WriterCranbury, NJ$55,000–$60,000 / yearComprehend and apply relevant evidenced-based medical literature, clinical practice guidelines, and disease-state information for the development of content across various therapeutic areas (eg, identify levels of evidence, clinical trial data, clinical utility of therapeutic choices and unmet needs in treatment landscapes, product-specific education). As a Medical Writer with the Enterprise Content Team at MJH Life Sciences, you will play a vital role in developing educational content for healthcare professional audiences.
Independent Contractor, Medical Writer, Publications Vaniam GroupIndependent Contractor, Medical Writer, PublicationsThe Medical Writer is responsible for developing high-quality content for an array of projects, including abstracts, presentations, manuscripts, advisory boards, scientific platforms, gap analyses, literature summaries, slide sets, and training materials. Develop high-quality content for an array of projects, including publications (eg, abstracts, presentations, and manuscripts), advisory boards, scientific platforms, gap analyses, literature summaries, slide sets, and training materials.