Kiniksa Pharmaceuticals International PlcPrincipal Medical Writer Kiniksa Pharmaceuticals International PlcPrincipal Medical Writerlexington, MA$178,000–$189,000 / yearThe ideal candidate will bring strategic insight, scientific rigor, and cross-functional collaboration to ensure timely and compliant delivery of key documents that support our innovative pipeline. Responsibilities (including, but not limited to): Author, review, and manage a broad range of documents including: Clinical study protocols, investigator brochures (IBs), clinical study reports (CSRs).
Daley and AssociatesMedical Technical Writer Daley and AssociatesMedical Technical WriterBoston, MA$40–$45 / hourThe ideal candidate will have 3-5+ years of technical writing experience within life sciences, with specific experience supporting medical devices and/or IVD products. The Technical Writer will be responsible for developing, revising, and maintaining high-quality technical documentation across multiple product lines.
MindlanceIT - Technical Writer 2 MindlanceIT - Technical Writer 2Boston, MARemoteSummary: The main function of a Technical Writer is to write technical materials, such as equipment materials, appendices, or operating and maintenance instructions. May be asked to troubleshoot complex problems and engages others in problem-solving strategies to identify practical and effective solutions to complex issues.
LancesoftVigilance Writer LancesoftVigilance WriterActon, MARemote$43The Global Product Monitoring Vigilance Report Writer develops, establishes, and maintains quality assurance methodologies, systems, and medical device industry best practices which meet customer, regulatory, and client requirements;serves as a post-market vigilance (reportable event) and surveillance subject matter expert and representative to improve awareness, visibility, and communication on quality/compliance initiatives to support departmental, divisional, and corporate quality goals and priorities;works on problems of diverse scope where analysis of data requires evaluation of identifiable factors;demonstrates good judgment in selecting methods and techniques for obtaining solutions;and networks with senior internal and/or external personnel in own area of expertise. Working knowledge/experience with global, multi-country vigilance reporting requirements for medical devices and demonstrated knowledge of country-specific differences and requirements.
Daley and AssociatesTechnical Writer - Med Device Daley and AssociatesTechnical Writer - Med DeviceBoston, MA$40–$45 / hourCreate and manage technical documentation using MadCap Flare, utilizing condition tags, variables, snippets, content reuse strategies, and multichannel publishing outputs (with a focus on PDF publishing). This role is responsible for developing, updating, and maintaining technical content, producing multi-channel outputs with a strong focus on PDF publishing, and collaborating with cross-functional teams.
IBSS CorporationNewTechnical Writer II IBSS CorporationTechnical Writer IIGloucester, MARemote$68,000–$72,000 / yearThe TDM division is responsible for providing web and mobile based applications, technical services and support for approximately 16,000 internal and external customers (fisheries management councils, state and USCG law enforcement, state fisheries management and other fishery management groups, and commercial fishing industry users). If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to the Talent Acquisition department at Recruiting@ibsscorp.com.
HonorVet TechnologiesNewTechnical Writer/ Instructional Designer HonorVet TechnologiesTechnical Writer/ Instructional DesignerBoston, MARemote$49.65–$49.65 / hourHonorVet Technologies (SDVOSB) is a certified veteran-owned staffing and workforce solutions company recognized for its industry certifications, commitment to quality talent acquisition, and excellence in delivering IT, healthcare, federal, state, and SLED (State, Local, and Education) staffing services, helping organizations build reliable, compliant, and high-performing teams across mission-critical sectors. This is a highly collaborative role that requires working closely with cross-functional teams including product management, engineering, regulatory affairs, design, and subject matter experts.
Kforce Inc.NewTechnical Writer Kforce Inc.Technical WriterActon, MARemote$48–$48Employee pay is based on factors like relevant education, qualifications, certifications, experience, skills, seniority, location, performance, union contract and business needs. A strong background in technical writing is required, along with 1-2 years of experience creating user-facing instructional manuals and working in Adobe Creative Cloud.
Hilco GlobalNewWriter/Editor Hilco GlobalWriter/EditorQuincy, MA$50,000–$60,000 / yearHilco Global, a subsidiary of ORIX Corporation USA, is a diversified financial services company that delivers integrated professional services and capital solutions that help clients maximize value and drive performance across the retail, commercial and industrial, real estate, manufacturing, brand and intellectual property sectors, and more. Hilco Valuation Services, LLC is an industry leader performing business asset appraisals covering consumer, retail and industrial inventories, machinery & equipment, real estate, and intangible assets.
Mondelez InternationalNewR-168491 Full Time Nabisco Merchandiser/Order Writer - Lowell, MA Mondelez InternationalR-168491 Full Time Nabisco Merchandiser/Order Writer - Lowell, MAPeabody, Massachusetts$23.44–$25.44As a Brand Execution Merchant, you’ll bring world-famous snacks like Oreo, Ritz, belVita, Chips Ahoy!, and Triscuit to life in-store – building relationships, stocking shelves, executing displays, and ensuring shoppers always find their favorite snacks right where they expect them. We're leading the future of snacking with iconic global and local brands such as Oreo, Ritz, LU, Clif Bar and Tate's Bake Shop biscuits and baked snacks, as well as Cadbury Dairy Milk, Milka and Toblerone chocolate.
Mondelez InternationalR-162831 Full Time Nabisco Merchandiser/Order Writer Mondelez InternationalR-162831 Full Time Nabisco Merchandiser/Order WriterBrockton, Massachusetts$19–$21We're leading the future of snacking with iconic global and local brands such as Oreo, Ritz, LU, Clif Bar and Tate's Bake Shop biscuits and baked snacks, as well as Cadbury Dairy Milk, Milka and Toblerone chocolate. Join our team of Full Time Nabisco Merchandiser/Order Writers and fulfill the merchandising needs of our customers through communication & relationship building, stocking store shelves, and maintaining or changing out displays.
Victory Capital Holdings IncMarketing Content Writer and Editor Victory Capital Holdings IncMarketing Content Writer and Editorboston, MA$72,250–$85,000 / yearTarget Compensation:The target base salary range for this position is $72,250 - $ 85,000.Salaries are determined based on internal equity, internal salary ranges, market data/ranges, applicant's skills and prior relevant experience, certain degrees, and certifications. Marketing Content Writer and EditorSan Antonio, TX | Boston, MAAbout Victory Capital:Victory Capital (NASDAQ: VCTR) is a diversified global asset management firm.
MMSNonclinical Writer MMSNonclinical WriterBoston, MARemoteFull timeRoles and Responsibilities:Strong experience with development and writing of nonclinical documents (eg, Module 2.4 and 2.6 eCTD submission documents, Investigator’s Brochure [IB], Nonclinical Study Reports, Meeting Requests, Briefing Documents, RTQs). Lead projects independently with minimal oversight, lead the writing (structure, content and messaging) of nonclinical documents, ensure the nonclinical package aligns with current regulatory guidelines and meets scientific integrity.
Mondelez InternationalNewFull Time Nabisco Merchandiser/Order Writer Mondelez InternationalFull Time Nabisco Merchandiser/Order WriterBillerica, MAWe have corporate offices, sales, manufacturing and distribution locations throughout the U.S. to ensure our iconic brands—including Oreo and Chips Ahoy! cookies, Ritz, Wheat Thins and Triscuit crackers, and Swedish Fish and Sour Patch Kids confectionery products —are close at hand for our consumers across the country. As a Brand Execution Merchant, you’ll bring world-famous snacks like **Oreo, Ritz,** **belVita** **, Chips** **Ahoy!,** **and Triscuit** to life in-store **–** building relationships, stocking shelves, executing displays, and ensuring shoppers always find their favorite snacks right where they expect them.
Alliance Technical GroupNewTech Services Writer I Alliance Technical GroupTech Services Writer ISharon, MA$22–$25 / hourThe primary duties of the Technical Services Writer include technical writing of proposals, test plans and reports for source testing projects. Draft reports are. then provided to the project manager or technical services manager for review prior to submittal to the clients.
HonorVet TechnologiesNewVigilance Writer HonorVet TechnologiesVigilance WriterActon, MARemote$46.55–$46.55 / hourJob Description: The Global Product Monitoring Vigilance Report Writer develops, establishes, and maintains quality assurance methodologies, systems, and medical device industry best practices which meet customer, regulatory, and client requirements; serves as a post-market vigilance (reportable event) and surveillance subject matter expert and representative to improve awareness, visibility, and communication on quality/compliance initiatives to support departmental, divisional, and corporate quality goals and priorities; works on problems of diverse scope where analysis of data requires evaluation of identifiable factors; demonstrates good judgment in selecting methods and techniques for obtaining solutions; and networks with senior internal and/or external personnel in own area of expertise. With strong delivery capabilities and rapid turnaround times, we support contract, direct hire, project-based, and consulting staffing needs across clinical research, pharmacovigilance, regulatory affairs, quality assurance, quality control, medical affairs, manufacturing, validation, and scientific operations.
Prime MedicineSenior Manager, Medical Writing Prime MedicineSenior Manager, Medical WritingWatertown, MA$153,096–$188,095 / yearReporting to the Head of Medical Writing, this individual will partner closely with Clinical Development, Regulatory Affairs, Research, and other cross-functional teams to ensure accurate, consistent, and timely documentation supporting global clinical trials and regulatory submissions. Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types.
BostonGene CorpDirector, Medical Communications BostonGene CorpDirector, Medical CommunicationsMACross-Functional Collaboration: Supports the development of medical communications for external audiences, including press releases, white papers, and materials for pharma and biotech clients, investors, regulatory agencies, and healthcare providers. Strategic Communication Development: Develop and implement comprehensive communication strategies that align with the company's business goals, including client interactions, congress strategy, publication strategic planning and regulatory submissions.
EBSCOClinical/Medical Editor II EBSCOClinical/Medical Editor IIIpswich, Massachusetts$68,070–$97,240 / yearYour Opportunity: The Medical-Surgical/Home Health Clinical Editor will be responsible for supporting the Section Editors in overseeing the development of high-quality content within specific content domain(s), applying both clinical knowledge/experience and the principles of evidence-based practice. The candidate must have the ability to analyze and critically appraise medical, nursing and allied health research and literature, write clinical topics and edit work produced by clinical editorial team.
Vertex Pharmaceuticals IncAssociate Director Medical Writing (Hybrid) Vertex Pharmaceuticals IncAssociate Director Medical Writing (Hybrid)Boston, MARemote$157,600–$236,400 / yearAt Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. This role applies advanced technical expertise and develops solutions to complex problems, fosters interdisciplinary understanding, and integrates Medical Writing Science department activities with those of other departments.
Ipsen SANewDocument Specialist Ipsen SADocument SpecialistCambridge, MA$91,500–$134,200 / yearExperience as a clinical/regulatory/safety Medical Writer, i.e., preparation of a wide range of clinical/regulatory documents including Clinical Study Reports, Protocols, Subject Narratives, Investigator Brochures, Regulatory Submission Modules, Safety Reports, and Manuscripts. Working with minimal guidance, the incumbent will take accountability for delivering regulatory documents, working effectively and closely with key content owners in the relevant functions.
MMSSenior Biostatistician - Remote (US) MMSSenior Biostatistician - Remote (US)Boston, MARemoteFull timeLeads projects (all phases and even a program of studies) and smaller submissions, manages client meetings, CRMs, collaborates well with regulatory, PMs and sponsor. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive.
MMSPrincipal Biostatistician - Remote MMSPrincipal Biostatistician - RemoteBoston, MARemoteFull timeProduce and present external company presentations providing industry visibility for the organization; Continually suggesting solutions to solve issues in tune with organizational direction. Lead complex projects, programs and submissions, manages client meetings, CRMs, collaborates well with regulatory, PMs and sponsors.
Celldex Therapeutics IncSr. Clinical Scientist/Associate Director, Clinical Science Celldex Therapeutics IncSr. Clinical Scientist/Associate Director, Clinical ScienceNeedham, MA$133,579–$199,501 / yearAuthor (and/or work with external medical writers to develop) clinical documents including but not limited to clinical protocols/amendments, briefing documents, IND annual reports, Investigators Brochures, clinical study reports, scientific presentations including abstracts, posters and manuscripts. Ensure clinical data collection proceeds in a manner consistent with strategic objectives and regulatory requirements for reporting (i.e., collaborate with statisticians to produce statistical analysis plans and data displays; provide input to CRF design and data management processes; perform periodic review of clinical data).
ImCheck Therapeutics SASClinical Trial Administrator ImCheck Therapeutics SASClinical Trial AdministratorCambridge, MA$67,500–$99,000 / yearResponsible for tracking, collecting and disclosure of expenses in compliance with regulations in force: EFPIA disclosure code (Europe), Sunshine Act (US):Collect all the information related to reportable transfers of value (ToV) to Healthcare Professionals (HCPs) & Healthcare Organizations (HCOs) in the Group Transparency system .Ensure complete data tracking by the SP with the Data Collection Template (DCT).Check the data received from the SP.Ensure the information is properly recorded in the Data Transparency system (COLLECT), implement corrective actions where needed. Perform continuous oversight of the Service Provider (SP)/Ipsen TMF activities, according to Ipsen SOP.Coordinate the TMF Quality Check (as per Ipsen SOP) with the SP/Ipsen to maintain data integrity and to ensure eTMF inspection/audit readiness.
Ipsen SAClinical Trial Administrator Ipsen SAClinical Trial AdministratorCambridge, MA$67,500–$99,000 / yearResponsible for tracking, collecting and disclosure of expenses in compliance with regulations in force: EFPIA disclosure code (Europe), Sunshine Act (US): Collect all the information related to reportable transfers of value (ToV) to Healthcare Professionals (HCPs) & Healthcare Organizations (HCOs) in the Group Transparency system. Coordinate and conduct in-house and external clinical operations activities: Generate contract templates within the Ipsen dedicated system (ARIBA), follow-up until the clinical study contracts are signed and secure proper filing and archiving of all fully executed contracts.
Harvard UniversityNewManaging Editor, Content Strategy Harvard UniversityManaging Editor, Content StrategyBoston, MARemoteBy driving a disciplined, data-informed approach to content lifecycle management, this role directly supports and protects a multi-million-dollar licensing business that depends on the delivery of current, reliable health information to long-term partners. Our portfolio of innovative medical education opportunities is available to learners around the world and includes live in-person programs, hybrid courses, self-paced online learning, digital products, educational webinars, podcasts, and printed materials.
US Tech Solutions, Inc.Clinical Reviewer Outpatient Registered Nurse # 26-10731 US Tech Solutions, Inc.Clinical Reviewer Outpatient Registered Nurse # 26-10731Canton, MA$50–$50 / hourKey Responsibilities/Duties – what you will be doing:Provides all aspects of clinical decision making and support needed to perform utilization management, medical necessity determinations and benefit determinations using applicable coverage documents, purchased clinical guidelines or Medical Necessity Guidelines for clinically complex services / coverage requests in a consistent manner and within established, product specific time frames. Interfaces between Precertification staff and providers when issues arise regarding policy interpretation, potential access availability or other quality assurance issues to ensure that members receive coverage decisions timely within all accrediting and regulatory guidelines.