TEMPORARY

FULL_TIME

CONTRACTOR

ADAPTED_NOW

YEAR

The role requires strong experience with MadCap Flare and structured content development, including reusable content strategies, variables, condition tags, and multi-channel publishing outputs. JOB SCOPE: The Technical Writer will be responsible for authoring, revising, and maintaining end-user documentation for medical devices in compliance with applicable regulatory and quality system requirements.

Job Title: Technical Writer Location: Boston area, MA (Hybrid) – 3 days a week onsite, 2 remote Duration: 6 months Start Date: March 30th JOB SCOPE: The Technical Writer will be responsible for authoring, revising, and maintaining end-user documentation for medical devices in compliance with applicable regulatory and quality system requirements. This person will support documentation such as Instructions for Use, User Manuals, Package Inserts, and Quick Reference Guides. The role requires strong experience with MadCap Flare and structured content development, including reusable content strategies, variables, condition tags, and multi-channel publishing outputs. The writer will collaborate cross-functionally with Regulatory Affairs, Engineering, Quality, and Marketing to ensure documentation accuracy, consistency, and compliance. This individual will also participate in design control activities, review risk and verification/validation documentation, and process updates through formal change control. Include Must Have Skills: • 3–5+ years of technical writing experience within medical device, IVD, or life sciences • Strong experience authoring end-user documentation such as IFUs, user manuals, package inserts, and quick reference guides • Advanced proficiency with MadCap Flare • Experience with structured content, version control, variables, condition tags, snippets, and content reuse strategies • Experience working within an FDA- and ISO-regulated environment • Understanding of QMS and controlled documentation processes • Experience supporting change control / ECO processes • Strong written and verbal communication skills • Ability to work cross-functionally with Regulatory, Quality, Engineering, and Marketing • Ability to manage multiple concurrent projects independently Education Requirements: • Bachelor’s degree or higher in English, Technical Writing, or related field Nice to have skills: • Familiarity with global labeling requirements including FDA, EU MDR, IVDR, and Health Canada • Experience with Adobe Acrobat • Experience with Adobe FrameMaker • Experience with graphics tools • Knowledge of Smartsheet

Black Diamond Networks

MedCap Flare Tech Writer

Adobe Acrobat

Adobe FrameMaker

Biology

Change Control

Communication Skills

Content Filtering Software

Content Structure

Cross-Functional

Document Management

Documentation

English Language

FDA Requirements

Graphics

Health Canada

Marketing

Medical Equipment

Multitasking

Presentation/Verbal Skills

Project/Program Management

Quality Engineering

Quality System Requirements (QSR)

Regulations

Regulatory Compliance

Risk

Source Code/Configuration Management (SCM)

Technical Writing

User Documentation

Validation Documentation

Validation Testing

Writing Skills

monster

PERMANENT

While an hourly range is posted for this position, an eventual hourly rate is determined by a comprehensive salary analysis which considers multiple factors including but not limited to: job-related knowledge, skills and qualifications, education and experience as compared to others in the organization doing substantially similar work, if applicable, and market and business considerations. We are seeking a Senior Technical Writer to lead the development and delivery of high-quality technical documentation supporting complex systems and enterprise applications.

JOB TITLE: Technical Writer - Senior JOB LOCATION: Remote WAGE RANGE*: $80k to $82,500k JOB NUMBER: 26-00547 REQUIRED EXPERIENCE: Minimum 8 years of experience in technical writing, editing, or documentation development Clearance: Active Secret Clearance JOB DESCRIPTION Position Overview We are seeking a Senior Technical Writer to lead the development and delivery of high-quality technical documentation supporting complex systems and enterprise applications. This role is responsible for producing a wide range of documentation including user guides, technical manuals, system documentation, and analytical reports. The position plays a key role in translating complex technical concepts into clear, structured, and user-friendly content while ensuring compliance with industry and program standards.<div> </div>Key Responsibilities<ul><li>Develop, edit, and maintain comprehensive technical documentation including user guides, reference manuals, and system documentation</li><li>Produce program maintenance manuals and document coding standards for complex systems and applications</li><li>Author research reports, technical summaries, and specialized publications using advanced technical language</li><li>Translate complex technical concepts into accessible, user-friendly content for diverse audiences</li><li>Lead the creation and management of digital content for online platforms, improving usability and user experience</li><li>Collaborate with engineers, developers, and subject matter experts to ensure technical accuracy and completeness</li><li>Ensure documentation aligns with industry standards, compliance requirements, and program objectives</li><li>Drive improvements in documentation processes, tools, and methodologies</li><li>Support documentation strategy and standardization across programs</li></ul><div>Required Qualifications</div><ul><li>Bachelor's degree in Technical Writing, Communications, Information Technology, or related field</li><li>Minimum 8 years of experience in technical writing, editing, or documentation development</li><li>Experience supporting complex systems, software applications, or data-driven platforms</li><li>Strong ability to write, edit, and organize technical content for both technical and non-technical audiences</li><li>Experience collaborating with cross-functional teams and subject matter experts</li></ul> Equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities * While an hourly range is posted for this position, an eventual hourly rate is determined by a comprehensive salary analysis which considers multiple factors including but not limited to: job-related knowledge, skills and qualifications, education and experience as compared to others in the organization doing substantially similar work, if applicable, and market and business considerations. Benefits offered include medical, dental and vision benefits; dependent care flexible spending account; 401(k) plan; voluntary life/short term disability/whole life/term life/accident and critical illness coverage; employee assistance program; sick leave in accordance with regulation. Benefits may be subject to generally applicable eligibility, waiting period, contribution, and other requirements and conditions. Benefits offered are in accordance with applicable federal, state, and local laws and subject to change at TCM's discretion.

<h2>About TCM</h2>
If you would like to…
<ul>
<li>Develop your skills</li>
<li>Improve your earnings potential</li>
<li>Gain greater control over your career</li>
</ul>
 The Computer Merchant, Ltd. (TCM) has provided Information Technology Solutions and enterprise staffing services to Fortune 1000, mid to small sized corporations, as well as Federal, state, and local governments for over 30 years. At The Computer Merchant (TCM), we are committed to your professional and financial success. We'll evaluate your background, experience and qualifications, and then recommend contract jobs that are the best match for your goals. Fast Facts & Recognition:
<ul>
<li>41 year track record of success deploying over 63,000 consultants and core employees in critical positions for Fortune 1000 companies</li>
<li>Access to over 11 million unique consultants nationwide</li>
<li>Centralized and dedicated client delivery team</li>
<li>Supplier Diversity Certification as a Veteran Business Enterprise</li>
</ul>

The Computer Merchant, LTD.

Senior Technical Writer

Coding Standards

Content Management

Documentation Standards

Enterprise Applications

Federal Laws and Regulations

Industry Standards

Information Technology & Information Systems

Maintain Compliance

Process Improvement

Reporting Skills

Secret Clearance

Standards Strategy

State Laws and Regulations

Support Documentation

Technical Editing

Technical Publications

Technical Research

Technical Support

Usability Engineering

User Interface/Experience (UI/UX)

UNKNOWN

FEED

Your ResponsibilitiesCreate compelling lesson content — develop scenarios, contexts, and topics that keep learners engaged and make vocabulary and grammar feel relevant and real. Write with precision — apply a strong grasp of English grammar, usage, and register to produce accurate, natural-sounding content that models the language learners are acquiring.

<img alt="" height="40" src="https://assets.jazz.co/customers/customer_20240206125052_WTHCWZGSS4CMNWQD/layout/20240313143002-Logo.png" width="240"/> Transparent Language is a leading provider of best-practice language-learning software for consumers, government agencies, educational institutions, and businesses. Since 1991, Transparent Language has helped millions of individuals learn new languages quickly, easily, and effectively. More than 12,000 schools and universities use our products. What You'll Do Design and build engaging digital ESL companion lessons that bring a client's curriculum to life. You'll take lesson objectives and transform them into interactive, motivating learning experiences for adult learners. We are looking for someone who can creatively leverage authentic materials and adapt them to fit learning goals and our existing language-learning software capability. Your Responsibilities<ul style="margin-bottom:11px"><li style="margin-bottom:11px">Create compelling lesson content — develop scenarios, contexts, and topics that keep learners engaged and make vocabulary and grammar feel relevant and real.</li><li style="margin-bottom:11px">Build fully functional digital lessons using proprietary authoring software, making smart use of available media, including audio, text, and graphics.</li><li style="margin-bottom:11px">Design for the platform — adapt lesson structures to get the most out of the authoring environment, always putting learning effectiveness first.</li><li style="margin-bottom:11px">Stay true to the methodology — ensure all content reflects the curriculum's communicative approach, presenting language in authentic, meaningful contexts.</li><li style="margin-bottom:11px">Write with precision — apply a strong grasp of English grammar, usage, and register to produce accurate, natural-sounding content that models the language learners are acquiring.</li><li style="margin-bottom:11px">Develop practice activities — create well-aligned activities such as multiple-choice, matching, and drag-and-drop exercises that reinforce each lesson's objectives.</li><li style="margin-bottom:11px">Review and quality-check all content for accuracy, level-appropriateness, and alignment to learning goals before release.</li><li style="margin-bottom:11px">Share your expertise — offer practical recommendations for improving the digital learning experience, drawing on your knowledge of adult ESL/EFL instruction and e-learning design principles.</li></ul>Desired experience and skills:<ul><li style="margin-left:8px">Must be a native speaker of English </li><li style="margin-left:8px">Have experience with instructional design in a web-based environment</li><li style="margin-left:8px">Have experience creating content for English learners at higher levels of proficiency</li><li style="margin-left:8px">Have experience using authentic materials in a language learning product</li><li style="margin-left:8px">Have the ability to work both independently and on a team, comfortable receiving input and iterating on a product</li><li style="margin-left:8px">Is willing to take responsibility and ownership of the tasks assigned</li><li style="margin-left:8px">Is willing to learn new skills as needed</li></ul> Tech requirements:<ul style="margin-bottom:11px"><li style="margin-bottom:11px;margin-left:8px">Windows-based computer or laptop</li></ul> We are an Equal Opportunity Employer.  Individuals with Disabilities and Protected Veterans are encouraged to apply.Powered by JazzHR

Transparent Language Inc.

Freelance: Digital English Lesson Author

partner JazzHR

OTHER

Must have at least 5 years of experience as a full time dedicated Technical Writer on a large, complex technical program, creating, editing, and producing extensive documents, reports, CDRLs, and briefings for diverse audiences, including senior leadership. Prepare, author, edit, and proof technical documents and program deliverables (e.g., system manuals, user guides, training materials, installation guides, proposals, reports) in accordance with the SOW and CDRLs.

his role supports the U.S. Air Force Cloud One Architecture and Common Shared Services contract and currently has an opening for a Technical Writer. Location: This position will be hybrid remote. Candidates will be required to work onsite as needed. Preferred candidates will be located near Hanscom AFB (Boston, MA).  Responsibilities:<ul><li>Prepare, author, edit, and proof technical documents and program deliverables (e.g., system manuals, user guides, training materials, installation guides, proposals, reports) in accordance with the SOW and CDRLs.</li><li>Ensure all documents conform to program standards, Data Item Description (DID) requirements, and applicable templates.</li><li>Create and maintain document templates using styles and formats in MS Word.</li><li>Work closely with engineers, developers, testers, Release Train Engineers, users, and other stakeholders to gather requirements, define content, and capture data and media for documentation.</li><li>Perform quality assurance reviews on all contractual documentation and deliverables, ensuring comments and customer feedback are fully addressed.</li><li>Format, review, and submit contract deliverables and reports, ensuring proper configuration management (CM) and version control in coordination with Data Management staff.</li><li>Oversee the collection, organization, editing, and revision of documentation supporting complex computer systems and networks.</li><li>Apply and help guide implementation of CMMI Maturity Level 3 best practices for documentation and quality.</li><li>Manage multiple documentation efforts simultaneously with strong attention to detail, quality, and on-time task completion.</li></ul>Requirements<ul><li>Bachelor’s Degree in a Technical, Writing, or related discipline and at least 8 years of relevant experience. Additional experience may be substituted for a degree.</li><li>Additional experience may be accepted in lieu of degree. </li><li>Active Secret clearance required   </li><li>US citizenship required </li><li>Bachelor’s Degree in a Technical, Writing, or related discipline and at least 8 years of relevant experience. Additional experience may be substituted for a degree.</li><li>Must have at least 5 years of experience as a full time dedicated Technical Writer on a large, complex technical program, creating, editing, and producing extensive documents, reports, CDRLs, and briefings for diverse audiences, including senior leadership.</li><li>Must have expert-level proficiency with advanced MS Word formatting and editing features, with extensive experience developing, managing, and refining large, complex technical documents and publications.</li><li>Must have direct experience working with system engineers, software engineers, and program management to translate technical information into clear, concise documentation including user manuals and reports.</li><li>Must demonstrate excellent grammar skills (including punctuation, spelling, and usage).</li><li>Must be an exceptional communicator, both verbally and in writing, able to convey information clearly and concisely, build rapport effectively, and understand, interpret, and explain highly technical concepts to diverse audiences.</li><li>Must have experience planning, prioritizing, and managing multiple tasks in a dynamic, fast-paced environment.</li><li>Must be proficient in Microsoft Word, Excel, and PowerPoint.</li><li>Must be capable of performing high-quality work both individually and as part of a team.</li><li>Must be a self-motivated problem solver who proactively takes initiative when issues arise.</li></ul>Preferred Qualifications<ul><li>Master’s Degree in a Technical, Writing, or related discipline.</li><li>Experience working on or with multi-disciplinary technical development teams.</li><li>Experience working on an agile program and team.</li><li>Extensive experience on a system/software development program compiling, editing, and publishing documentation.</li><li>Sound understanding of CMMI best practices and agile methodologies.</li></ul>BenefitsSES provides a competitive salary and the following benefits:<ul><li>Medical</li><li>Dental</li><li>Vision</li><li>AD&D</li><li>STD</li><li>LTD</li><li>Company paid Life Insurance</li><li>401k with employer contribution</li><li>Paid Time Off</li><li>Pet Insurance</li></ul>

Systems Engineering Solutions Corporation

Technical Writer

Workable

As aSenior Medical Communications Writer, you will be responsible for researching, writing, and editing publications based on Rhythm’s R&D and therapeutic areas, as well as managing freelance writers and vendors and contributing to overall publication strategy. Strong organizational skills / advanced project management and organizational skills and ability to work independently, prioritize, and multitask to meet timelines under changing conditions.

Company Overview Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases and provide meaningful support for healthcare providers and patients and their families. We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need. Their courage inspires us to challenge convention, ask bold questions and seek answers for them. Every day, we strive for excellence through our willingness to adapt, learn, and our tenacity to overcome barriers, together. Opportunity Overview As aSenior Medical Communications Writer, you will be responsible for researching, writing, and editing publications based on Rhythm’s R&D and therapeutic areas, as well as managing freelance writers and vendors and contributing to overall publication strategy. This position will also provide writing support for associated materials to the Global Scientific Communications department. Responsibilities and Duties<ul><li>Perform literature reviews and solicit input from medical, statistical, and operational resources as necessary to support data analysis and document content.</li><li>Oversee vendor- and freelance writer-generated publications, ensuring deliverables are timely and of high quality for internal reviewers and external authors.</li><li>Membership on Core Publication Team and help with overall publication strategy and planning.</li><li>Assist with review of data to ensure cleanliness/appropriateness for analysis, hypothesis testing, QA of statistical output, and data compilation to support data summaries/presentations.</li><li>Writing scientific publications (papers for peer-reviewed medical journals, abstracts, posters, and slide presentations). </li><li>Other writing responsibilities include internal educational scientific slide kits, conference reports, and field medical training materials.</li></ul> Qualifications and Skills<ul><li>BS/BA in scientific discipline preferred, advanced degree is a plus.</li><li>6+ years of related experience, with at least 2 years in a pharmaceutical environment.</li><li>Proven scientific writing skills (particularly experience with developing scientific peer-reviewed publications).</li><li>Ability to interpret and summarize complex tabular and graphical data sets and design post-hoc analyses.</li><li>Expert knowledge of document content preparation, including the use of style guides, medical dictionaries, and online medical writing resources.</li><li>Edits to achieve consistency with scientific communication platform, uses precise accurate language and grammar and has a high attention to detail.</li><li>Comfortable working with co-authors (both external and internal), with exceptional collaboration, written, and verbal communication skills. Independently resolves document content issues and addresses questions by resolving discrepancies.</li><li>Strong organizational skills / advanced project management and organizational skills and ability to work independently, prioritize, and multitask to meet timelines under changing conditions.</li><li>An understanding of drug development, clinical research, study designs, biostatistics, pharmacology, and medical terminology.</li><li>Experience in obesity or rare diseases preferable.</li></ul> This role is based out of our corporate office in Boston, Massachusetts. Rhythm operates in a hybrid-work model. Candidates applying must be willing and able to be in the Boston office in coordination with their department and business needs.This role may involve some travel. The expected salary range for this position is $135,000 - $215,000. Actual pay will be determined based on experience, level, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and company performance. This role may be eligible for benefits and other compensation such as restricted stock units. More about Rhythm We are a dynamic and growing global team spanning more than a dozen countries. At Rhythm we are dedicated to transforming the lives of patients living with rare neuroendocrine diseases by rapidly advancing care and precision medicines that address the root cause.  Our team is passionate about expanding access to reach more patients and developing novel therapies for other rare neuroendocrine diseases, including congenital hyperinsulinism. At Rhythm our core values are:<ul><li style="text-align:justify;margin-left:8px">We are committed to advancing scientific understanding to improve patients’ lives</li><li style="text-align:justify;margin-left:8px">We are inspired to tackle tough challenges and have the courage to ask bold questions</li><li style="text-align:justify;margin-left:8px">We are eager to learn and adapt</li><li style="text-align:justify;margin-left:8px">We believe collaboration and ownership are foundational for our success</li><li style="text-align:justify;margin-left:8px">We value the unique contribution each individual brings to furthering our mission</li></ul> Rhythm is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service, or any other class protected by state or federal law. Headquartered in Boston, Rhythm is proud to have been named one of the <a href="https://www.bostonglobe.com/magazine/top-places-work/2023/" rel="nofollow" style="color:#467886;text-decoration:underline">Top Places to Work</a> in Massachusetts.Powered by JazzHR

Rhythm Pharmaceuticals

Senior Medical Communications Writer - Publications

Summary: This role provides non-testing support to the Quality Control team, focusing on product validation activities and GMP documentation. Employee pay is based on factors like relevant education, qualifications, certifications, experience, skills, seniority, location, performance, union contract and business needs.

Kforce has a client that is seeking a Technical Writer (Quality Control Support) in Andover, MA.

Summary:
This role provides non-testing support to the Quality Control team, focusing on product validation activities and GMP documentation. The Technical Writer will collaborate with laboratory SMEs to support method validation, data review, and lifecycle management in a regulated environment.

Responsibilities:
<ul><li> Author and maintain method validation and supporting GMP documents</li><li> Partner with laboratory SMEs and cross-functional teams</li><li> Support assay improvement initiatives and project timelines</li><li> Use laboratory systems (e.g., LIMS) and standard documentation workflows</li></ul> Requirements:<ul><li> Bachelor's degree in a scientific discipline (Microbiology preferred)</li><li> Experience with GMP documentation in a biopharmaceutical setting</li><li> Strong technical writing, communication, and organizational skills</li><li> Detail-oriented with a solid understanding of QC and regulatory requirements</li></ul> <div>
 The pay range is the lowest to highest compensation we reasonably in good faith believe we would pay at posting for this role. We may ultimately pay more or less than this range. Employee pay is based on factors like relevant education, qualifications, certifications, experience, skills, seniority, location, performance, union contract and business needs. This range may be modified in the future.
 
 We offer comprehensive benefits including medical/dental/vision insurance, HSA, FSA, 401(k), and life, disability & ADD insurance to eligible employees. Salaried personnel receive paid time off. Hourly employees are not eligible for paid time off unless required by law. Hourly employees on a Service Contract Act project are eligible for paid sick leave. 
 
 Note: Pay is not considered compensation until it is earned, vested and determinable. The amount and availability of any compensation remains in Kforce's sole discretion unless 
 and until paid and may be modified in its discretion consistent with the law. 
 
 This job is not eligible for bonuses, incentives or commissions.
 
 Kforce is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status.
 
 By clicking “Apply Today” you agree to receive calls, AI-generated calls, text messages or emails from Kforce and its affiliates, and service providers. Note that if you choose to communicate with Kforce via text messaging the frequency may vary, and message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You will always have the right to cease communicating via text by using key words such as STOP.
 </div>

Kforce is a solutions firm specializing in technology, finance and accounting, and professional staffing services. Our KNOWLEDGEforce® empowers top companies to achieve their digital transformation goals. We curate teams of technical experts who deliver solutions custom-tailored to each client’s needs. These scalable, flexible outcomes are shaped by deep market knowledge, thought leadership and our multi-industry expertise.
 
Our integrated approach is rooted in 60 years of proven success deploying highly skilled professionals on a temporary and direct-hire basis. Each year, approximately 18,000 talented experts work with the Fortune 500 and other leading companies. Together, we deliver Great Results Through Strategic Partnership and Knowledge Sharing®.

Kforce Inc.

Technical Writer (Quality Control Support)

kforce

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. Roles & ResponsibilitiesUnder minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias.

About MMS MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating. 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. MMS recognizes that a talented staff is what drives our business forward. Identifying and attracting top talent and continual training to strengthen core skills are essential to its core mission. At MMS, enthusiasm, collaboration, and teamwork are fostered, knowing that a global and diverse talent pool makes the company stronger. For more information, visit <a href="http://www.mmsholdings.com/" rel="nofollow">www.mmsholdings.com</a> or follow MMS on <a href="https://www.linkedin.com/company/mms-holdings-inc-/" rel="nofollow">LinkedIn</a>. Roles & Responsibilities<ul><li>Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias</li><li>Write and edit clinical development documents, including but not limited to, Informed Consent Forms and Clinical Protocols</li><li>Complete writing assignments in a timely manner</li><li>Maintain timelines and workflow of writing assignments</li><li>Practice good internal and external customer service</li><li>Highly proficient with styles of writing for various regulatory documents</li><li>Expert proficiency with client templates & style guides</li><li>Interact directly and independently with client to coordinate all facets of projects; competent communication skills for projects</li><li>Contribute substantially to, or manages, production of interpretive guides</li><li>Take ownership of a given assignment, proactively consulting other project team members and other department representatives for information or guidance as necessary</li><li>Mentor medical writers and other members of the project team who are involved in the writing process</li></ul>Requirements<ul><li>At least 3 years of previous experience in the pharmaceutical industry</li><li>Must have at least 3-5 years of industry regulatory writing and clinical medical writing experience</li><li>The ideal candidate would hold a Bachelors, Masters, or Ph.D. in scientific, medical, clinical discipline</li><li>Oncology, General Medicines, Infectious Diseases and Vaccine experience preferred </li><li>Substantial informed consent and clinical study protocol experience, as lead author, required</li><li>Experience leading and managing teams while authoring regulatory documents with aggressive timelines</li><li>Experienced in understanding complex clinical information</li><li>Translate complex medical and scientific information into clear, patient-friendly, language  </li><li>Experienced in collaboration and cross-functional communication</li><li>Exceptional writing skills are a must</li><li>Excellent organizational skills and the ability to multi-task are essential prerequisites</li><li>Candidate must be an expert in MS Word, Excel, PowerPoint, and related word processing tools</li><li>Experience being a project lead, or managing a project team</li><li>Strong understanding of federal regulations, Good Clinical Practices, and ICH guidelines a plus</li><li>Not required, but experience with orphan drug designations and PSP/PIPs a plus</li></ul>Powered by JazzHR

Senior ICF Writer (Remote)

Author Jobs in Cambridge, MA