JobotNewCustoms Entry Writer JobotCustoms Entry WriterLong Beach, CA$26–$32 / hourThe successful candidate will be responsible for preparing, compiling and managing all documentation and records required to clear goods through the United States Customs Service (USCS), including negotiating with, and presenting declarations to, foreign and domestic customs officials. Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal.
Kforce Inc.NewUX Writer - Senior Level Kforce Inc.UX Writer - Senior LevelSan Antonio, TX$38–$45This role independently leverages human-centered design, user testing, content design principles, omnichannel content strategy, SEO best practices, accessibility guidelines and USAA brand and style guidelines to create content and execute holistic digital content experiences to help solve member problems and achieve business goals. Description: This user experience role creates quality, high performing content to enable innovative, cohesive and compliant digital experiences that serve the needs of our members, member service representatives and business partners.
Butler America AerospaceNCR Writer Butler America AerospaceNCR WriterWest Lafayette, IN$25–$29 / hourContractorResponsibilities: Assist with Technical Writing assignments involving generation of Nonconformance Reports (NCRs), Inspection Plans / Control Plans, First Article Inspections (FAIs), and Material Review Board dispositions (MRBs). As our company continues to expand their new operation in West Lafayette, IN, we are seeking a Contract Technical Writer in the Quality department who provides support to internal customers related to product non-conformance identification, investigation, and disposition.
Pinnacle Technical ResourcesTechnical Writer - Intermediate Pinnacle Technical ResourcesTechnical Writer - IntermediateHouston,, Texas$30–$35 / hourContractorThe specific compensation for this position will be determined by a number of factors, including the scope, complexity and location of the role as well as the cost of labor in the market; the skills, education, training, credentials and experience of the candidate; and other conditions of employment. This role requires excellent communication skills, a strong understanding of technical concepts, and the ability to translate complex information into clear and concise documentation.
DCS CorporationNewTechnical Writer, Senior DCS CorporationTechnical Writer, SeniorBedford, MA$90,220–$125,000 / yearCommand, Control, Communications, and Battle Management (C3BM) has been tasked with delivering an integrated Department of the Air Force (DAF) Battle Network providing resilient decision advantage and enabling the USAF, USSF, Joint, and Coalition Force to win against the pacing challenge. C3BM’s main efforts are Architecture and Systems Engineering (ASE), Operational Response Team (ORT), and multiple mission integration teams such as Air, Maritime and multiple acquisitions consisting of both the Advanced Battle Management System (ABMS) and Space.
ECLARONewQuality - Technical writer ECLAROQuality - Technical writerNew Brunswick, NJ$42.85–$45.45 / hourResponsibilities:Co-authors/ authors scientific content for CTD Quality sections aligned with regulatory strategy for clinical and life-cycle CMC regulatory submissions and responses to health authority questions based on high quality technical reports. Partner with SMEs across CTDO to identify source documents and align delivery of approved technical documents in accordance to project timelines and aligned with CTD requirements and regulatory strategy.
Famous Smoke ShopNewMarketing Content Writer / SEO Copywriter Famous Smoke ShopMarketing Content Writer / SEO CopywriterEaston, PAThis role creates short-form and long-form copy for digital and print platforms, including website content, product pages, category pages, landing pages, email, SMS, catalog, social media, video scripts, blogs, guides, and promotional campaigns. Famous Cigars, rooted in Famous Smoke Shop-PA, Inc. and the premium cigar industry since 1939, is a growing Easton, PA business spanning retail, catalog, e-commerce, and Leaf Restaurant & Bar, where we bring together product knowledge, hospitality, customer service, and a team-focused culture.
Hendrick Automotive Group CorporateAutomotive Collision Center Estimator/Auto Body Service Writer Hendrick Automotive Group CorporateAutomotive Collision Center Estimator/Auto Body Service WriterCharlotte, North CarolinaFull timeWork includes inspection of customer vehicles and frequent movement around the body repair shop to convey information between customers and Collision Center Technicians. Frequently interacts with customers, Collision Center Manager, Collision Center Technicians, and Company personnel.
Napleton Northlake Chrysler Dodge Jeep RamAutomotive Service Advisor/Writer Napleton Northlake Chrysler Dodge Jeep RamAutomotive Service Advisor/WriterLake Park, FLFull timeThey greet and consult customers on service needs, perform a thorough vehicle walk around inspection as part of the write-up, sell and up sell services by emphasizing value, keep customers updated on services, field all live service calls, and take ownership of the customer’s experience by carrying out those additional assignments that allow the dealership to leave an impressionable experience with the customer. As a Service Advisor, you will be experienced and aware of the latest customer service practices and be a persistent problem solver.
Gillman Chrysler Jeep Dodge RamAutomotive Service Advisor/Writer Gillman Chrysler Jeep Dodge RamAutomotive Service Advisor/WriterHouston, TXFull timeGillman Chrysler Jeep Dodge Ram in Houston is looking for experienced Service Advisors to join their industry leading service team. Service Advisors remain involved with the delivery of the vehicle to the customer upon completion to ensure all customer concerns can be addressed.
Jacksonville Chrysler Jeep Dodge Ram of ArlingtonAutomotive Service Advisor/Writer - Express Lane Jacksonville Chrysler Jeep Dodge Ram of ArlingtonAutomotive Service Advisor/Writer - Express LaneSt. Augustine, FLFull timeExpress Lane Service AdvisorJacksonville Chrysler Jeep Dodge Ram Arlington is looking for an Express Service Advisor to join their team! Experience in a Express Lane Advisor or Service Advisor role strongly preferred.
Lithia Chrysler Dodge Jeep Ram Of Corpus ChristiAutomotive Service Advisor/Writer Lithia Chrysler Dodge Jeep Ram Of Corpus ChristiAutomotive Service Advisor/WriterCorpus Christi, TXFull timeThey greet and consult customers on service needs, perform a thorough vehicle walk around inspection as part of the write-up, sell and up sell services by emphasizing value, keep customers updated on services, field all live service calls, and take ownership of the customers experience by carrying out those additional assignments that allow the dealership to leave an impressionable experience with the customer. Lithia Chrysler Jeep Dodge of Corpus Christiis looking to add motivated Automotive Service Advisors to their dynamic team!
Franklin Chrysler Dodge Jeep RamAutomotive Service Advisor/Writer Franklin Chrysler Dodge Jeep RamAutomotive Service Advisor/WriterFranklin, TNFull timeThey greet and consult customers on service needs, perform a thorough vehicle walk around inspection as part of the write-up, sell and up sell services by emphasizing value, keep customers updated on services, field all live service calls, and take ownership of the customers experience by carrying out those additional assignments that allow the dealership to leave an impressionable experience with the customer. Over the years, Franklin Chrysler Dodge Jeep RAM has established a reputation for providing the greater Franklin, Tennessee area with outstanding service.
Hendrick Automotive Group CorporateDodge Service Writer Hendrick Automotive Group CorporateDodge Service WriterCary, North CarolinaFull timeWork includes inspection of customer vehicles and frequent movement around the Service Department to convey information between customers and service technicians. Frequently interacts with customers, service manager and service technicians, and employees from various departments in the dealerships.
TravelNurseSourceNewTravel Nurse RN - Nurse Manager in The Lakes, NV TravelNurseSourceTravel Nurse RN - Nurse Manager in The Lakes, NVThe Lakes, NVRemoteThis fully remote opportunity is ideal for a highly skilled clinical science writer with extensive experience authoring Clinical Study Reports (CSRs), protocols, and regulatory submission documents across Phase I III studies. The ideal candidate is a hands-on writer who spends the majority of their time authoring and developing scientific and regulatory documents rather than primarily editing or managing teams.
Sterling Medical CorporationSecond Shift Proposal Writer and Proposal Coordinator Needed! Sterling Medical CorporationSecond Shift Proposal Writer and Proposal Coordinator Needed!Cincinnati, OH$58,005–$87,500 / yearGreat compensation and benefits with a dynamic Healthcare Firm located in Cincinnati, Ohio and Overseas. Update, coordinate and organize overall Proposal submission.
Company ConfidentialSpecification Writer 3 (HYBRID) - 28174 Company ConfidentialSpecification Writer 3 (HYBRID) - 28174Newport News, VA$45,718–$52,000Full timeWith a holistic approach to life-cycle maritime defense systems—from small watercraft to submarines, surface combatants and aircraft carriers—HII ensures a high state of readiness. Our capabilities range from C5ISR, AI and Big Data, cyber operations and synthetic training environments to fleet sustainment, environmental remediation and the largest family of unmanned underwater vehicles in every class.
Lancesoft IncMedical Information Lancesoft IncMedical InformationEwing Township, NJ$60–$69 / hourThe Contractor Medical Writer, Medical Information, Payer and Health Systems reports to the Associate Director/Director Med Info-PHS and supports the development and dissemination of Medical Information scientific content and materials to Payers, Healthcare Intermediaries and Health Systems across the assigned CLIENT portfolio of products. · Works closely with RW V&E Field, Medical Affairs Therapeutic Area team(s) and Medical Information Scientific Engagement Contact Center to guide creation and delivery of responses to unsolicited Medical Information Requests from Payers and Health Systems .
Haemonetics CorporationSenior Technical Writer Haemonetics CorporationSenior Technical WriterSeattle, WAFull timeContributes to the project strategy to meet target goals and milestones, evaluates resource allocation needs, and monitors project risks to determine the best mitigation path. For non-sales roles, employees will be eligible for a discretionary annual bonus, the target amount of which varies based on the applicable role, to be governed by the applicable plan terms.
J-U-B ENGINEERS, IncGrant Writer-Lead J-U-B ENGINEERS, IncGrant Writer-LeadKennewick, WA$82,000–$89,000 / yearFull timeWe are looking for a collaborative and solutions-oriented Grant Writer-Lead/Funding Specialist to serve within a multidisciplinary team, you will prepare comprehensive funding plans, federal and state grant applications, and technical reports. You will be the bridge between our clients' needs and the complex requirements of funding agencies, researching opportunities and managing the lifecycle of successful grants.
EchodyneTechnical Writer EchodyneTechnical WriterKirkland, WA$104,030–$155,839 / yearFull timeCollaborate with subject matter experts to gather and validate technical content; engage directly with products to gain hands-on understanding of documentation needs. This role works closely with engineers and subject matter experts (SMEs) to translate complex technical concepts into accessible content for a range of audiences.
AMAZON DEVELOPMENT CENTER U.S., INC.,Tech Writer-Tech III - AMZ9706813 AMAZON DEVELOPMENT CENTER U.S., INC.,Tech Writer-Tech III - AMZ9706813Seattle, WA$126,797–$170,200 / yearFull timeMust have one year of experience in the following skills: (1) designing and producing content for a technical audience, such as Software Engineers, System Administrators, or IT professionals; (2) using content publishing tools to write, format, manage, and publish technical content on the web; (3) working knowledge of at least two of the following programmer languages: Python, Java, C#, Node.js, or C/C++. Be the first "customer" - use subject-matter expertise to review planning and design documents to provide technical feedback on new features and workflows to improve the customer experience.
EnerSysTechnical Writer (Hybrid) EnerSysTechnical Writer (Hybrid)Kent, WAFull timeThis position is responsible for writing, illustrating and controlling customer-facing documentation including cabinet and kit installation manuals, technical bulletins, and troubleshooting guides for a wide variety of market applications. Ensure writing style of customer-facing documentation, procedure documentation, and test instructions is simple, clear, concise, grammatically correct, and written for the intended audience and purpose.
IREMedical Writer I - Medical Imaging IREMedical Writer I - Medical ImagingAt ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.
Swedish Orphan Biovitrum ABNewPrincipal Medical Writer Swedish Orphan Biovitrum ABPrincipal Medical WriterSan Diego, CA$160,000–$200,000 / yearAs a Principal Medical Writer, you will provide communication expertise and lead a strategy-driven approach to authoring of key clinical and regulatory documents and regulatory submissions, to ensure clarity, credibility and consistency of clinical information throughout submission packages and clinical programs, to facilitate regulatory assessment, and to achieve a product label that fulfills commercial needs. Key responsibilities: Lead a strategy-driven approach to authoring of the clinical components of regulatory submissions, ensuring a clear, concise, complete, credible and compelling scientific content aligned with the objective of the regulatory document.
IQVIAPrincipal Medical Writer IQVIAPrincipal Medical WriterDurham, North CarolinaTake a leading role in preparing assigned documents, including, but not limited to, confirming the scope of the task, confirming templates and specifications, negotiating and adhering to timelines, organizing document reviews, communicating directly with the customer. In-depth knowledge of the structural and content requirements of clinical study reports, protocols, and similar documents and ability to identify deficiencies, errors, and inconsistencies in documents.
IQVIASenior Medical Writer IQVIASenior Medical WriterDurham, North CarolinaTake a leading role in preparing assigned documents, including, but not limited to, confirming the scope of the task, confirming templates and specifications, negotiating and adhering to timelines, organizing document reviews, communicating directly with the customer. In-depth knowledge of the structural and content requirements of clinical study reports, protocols, and similar documents and ability to identify deficiencies, errors, and inconsistencies in a protocol or report.
Ionis Pharmaceuticals IncSenior 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.
MJH Healthcare Holdings LLCMedical Writer, Accredited Medical Education MJH Healthcare Holdings LLCMedical Writer, Accredited Medical EducationNYRemote$85,000–$95,000 / yearWrite and edit across multiple deliverables, including peer-reviewed publications, trade journal articles, monographs, slide decks, scripts, and digital programs. This role involves translating complex scientific and clinical information into clear, engaging content while ensuring accuracy, regulatory compliance, and alignment with relevant professional society (e.g.
Thermo Fisher Scientific IncMedical Writer - Medical Information Thermo Fisher Scientific IncMedical Writer - Medical InformationWilmington, NCKnowledge, Skills, and Abilities: • Solid medical writing skills, including grammatical, editorial and proofreading skills • Ability to interpret and present complex data accurately and concisely • Effective administrative, organizational and planning skills; attention to detail and quality • Ability to work on own initiative and effectively within a team • Effective oral and written communication skills • Great judgment and decision-making skills • Good computer skills and skilled with client templates; good knowledge of document management systems and other relevant applications (e.g. Experience with Medical Information (equivalent to 2+ years) Previous experience that provides the knowledge, skills and abilities to perform the job (comparable to 2+ years) Experience working in the pharmaceutical/CRO industry preferred.
BioMarin Pharmaceutical IncSenior Medical Writer BioMarin Pharmaceutical IncSenior Medical WriterCA$142,100–$195,360 / yearntttttSearch JobsntttttntttttLocationntttttntttttSearch RadiusnttttttttttnttttttWithin 25 milesnttttttWithin 50 milesnttttttWithin 100 milesnttttttWithin 250 milesnttttttWithin 500 milesnttttttWithin 1,000 milesnttttttWithin 2,000 milesnttttttWithin 5,000 milesntttttntttttntttttntttttntttt. nttttttDIN numbernttttttnttttttnttttttnttttt.
Inizio Engage XDNewPrincipal Medical Writer Inizio Engage XDPrincipal Medical WriterPhiladelphia, PennsylvaniaAs a Principal Medical Writer, you will be the trusted, client‑facing lead for one or more flagship accounts, shaping high‑quality scientific content that makes a impact in life sciences education. You'll create accurate, compelling, and referenced materials across a broad range of training deliverables-such as self‑study curricula and interactive workshops.
IREPrincipal Medical Writer IREPrincipal Medical WriterAs 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.
MJH Life SciencesMultispecialty Medical Writer, Accredited Medical Education MJH Life SciencesMultispecialty Medical Writer, Accredited Medical EducationRemoteWrite and edit across multiple deliverables, including peer-reviewed publications, trade journal articles, monographs, slide decks, scripts, and digital programs. This role involves translating complex scientific and clinical information into clear, engaging content while ensuring accuracy, regulatory compliance, and alignment with relevant professional society (e.g.
SorceroNewContract Medical Writer SorceroContract Medical WriterTheir role is to review and develop AI draft manuscripts to the level desired by Sorcero and contribute to Sorcero validation work for increasing the speed of evidence to clinical practice. By joining our team, you will play a critical role in our growth and success by collaborating with our network of passionate entrepreneurs to build a scalable, impactful organization.
BioMarin Pharmaceutical IncMedical Writer BioMarin Pharmaceutical IncMedical WriterSan Rafael, CA$74,100–$100,000 / yearntttttSearch JobsntttttntttttLocationntttttntttttSearch RadiusnttttttttttnttttttWithin 25 milesnttttttWithin 50 milesnttttttWithin 100 milesnttttttWithin 250 milesnttttttWithin 500 milesnttttttWithin 1,000 milesnttttttWithin 2,000 milesnttttttWithin 5,000 milesntttttntttttntttttntttttntttt. nttttttDIN numbernttttttnttttttnttttttnttttt.
Syneos HealthNewSr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology Preferred Syneos HealthSr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology PreferredNew JerseyProvides strategic direction to cross-functional project teams with minimal oversight to ensure that clinical documents (eg, Investigators' Brochures [IBs], Clinical Study Reports [CSRs], and marketing authorization submission documents) accurately and consistently present key data-driven clinical messages in accordance with program goals and regulatory requirements. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology PreferredSyneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success.
Thermo Fisher Scientific IncSenior Medical Writer Thermo Fisher Scientific IncSenior Medical WriterWilmington, NCKnowledge, Skills, Abilities: Excellent data interpretation and medical writing skills, including grammatical, editorial, and proofreading skills Ability to interpret and present complex data accurately and concisely Ability to work on own initiative and effectively within a team Excellent administration, attention to detail, organizational, planning, and problem-solving skills Strong project management skills Excellent oral and written communication skills with strong presentation skills Significant knowledge of global, regional, national and other document development guidelines Great judgment and decision-making skills; strong negotiation skills Excellent computer skills and skilled with client templates; good knowledge of document management systems and other relevant applications (e.g. Experience working in the pharmaceutical/CRO industry preferred Additional qualifications in medical writing or medical information advantageous Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job.
VeristatSenior Medical Writer VeristatSenior Medical WriterMassachusettsAutomated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process. The Senior Medical Writer works under the direction of Medical Writing management and collaborates with cross-functional internal and external document production teams.
Celldex Therapeutics IncAssociate 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.
BiofireMedical Writer BiofireMedical WriterSalt Lake City, UT$95,000–$124,000 / yearIn addition, bioMérieux offers a competitive Total Rewards package that may include: · A choice of medical (including prescription), dental, and vision plans providing nationwide coverage and telemedicine options · Company-Provided Life and Accidental Death Insurance · Short and Long-Term Disability Insurance · Retirement Plan including a generous non-discretionary employer contribution and employer match. This role is responsible for developing clear, accurate, and scientifically sound documents that effectively communicate complex clinical, medical, and scientific data to healthcare professionals, internal stakeholders, and external audiences.
ProPharma Group Holdings LLCPrincipal Medical Writer, Oncology ProPharma Group Holdings LLCPrincipal Medical Writer, OncologyChicago, ILWith 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.
ProPharma Group Holdings LLCPrincipal Medical Writer, Cardio/Metabolic Health ProPharma Group Holdings LLCPrincipal Medical Writer, Cardio/Metabolic HealthChicago, ILWith 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.
Praxis Precision MedicinesNewSenior Medical Writer Praxis Precision MedicinesSenior Medical WriterCollaborates 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 . At Praxis we share a common vision of reshaping the human condition into a more freeing and fulfilled existence by developing high impact medicines for patients and families affected by and living with complex brain disorders.
Syneos Health IncSenior Medical Writer - Regulatory Documents - CSR /Protocol - Late Phase Syneos Health IncSenior Medical Writer - Regulatory Documents - CSR /Protocol - Late PhaseMorrisville, NCInteracts and builds good working relations with clients, department head, and peers in data management, biostatistics, regulatory affairs, and medical affairs as necessary to produce writing deliverables. We are passionate about developing our people through career development and progression, supportive and engaged line management, technical and therapeutic area training, peer recognition, and total rewards program.
Precision Medicine Group LLCMedical Writer, Medical Communications Precision Medicine Group LLCMedical Writer, Medical CommunicationsNYRemote$80,000–$110,000 / yearYou conduct outstanding literature searches - using appropriate search strategy, keywords, and a variety of sources when researching journal articles, and medical research papers. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs.
Worldwide Clinical Trials Holdings IncSenior Medical Writer - US/Europe - Remote Worldwide Clinical Trials Holdings IncSenior Medical Writer - US/Europe - RemoteNCRemotePrepare and lead the medical writing team on Phase I-IV study documents such as protocols and protocol amendments, informed consent documents and assents, complete clinical trial reports (CTRs), CTR narratives, Investigator Brochures, and other study-related documents in accordance with regulatory requirements (USA, Europe and/or ROW) and WCT SOPs. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.
St. Jude Children's Research Hospital IncSenior 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.
Syneos HealthMedical Writer II - Publications Syneos HealthMedical Writer II - PublicationsIndianaInteracts and builds good working relations with clients, department head, and peers in data management, biostatistics, regulatory affairs, and medical affairs, as necessary, to produce writing deliverables. • We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
GeneDX LLCPrincipal Medical Writer GeneDX LLCPrincipal Medical WriterCedar Knolls, NJRemote$160,000–$170,000 / yearWith over 20 years of expertise in diagnosing rare disorders and diseases, and pioneering work in the identification of new disease-causing genes, our commitment to genetic disease detection, discovery, and diagnosis is based on sound science and is focused on enhancing patient care. Through both internal research efforts and global collaborations, we have identified and published hundreds of new disease-gene relationships and developed novel tools for genomic data analysis.