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  • Sr. Medical Writer (Remote/Sponsor

    SUMMARY OF RESPONSIBILITIES: The Medical Writer role will collaborate with internal and external key team partners to develop clinical documents, abstract and publications that are aligned with the Company objectives. This is a hands-on position that primarily includes writing and critically editing scientific manuscripts, abstracts, and podium presentations. . PRIMARY RESPONSIBILITIES: · Generate content in collaboration with authors/collaborators for protocols, investigator's brochure, clinical study reports, safety updates, abstracts, posters, orals, manuscripts, and slide sets working from various data sources · Performs Quality Control checking and proof reading of all required documents to meet customer expectation · Manage multiple documents across different molecules/projects and obtain feedback from all key partners to define and implement documents strategies · Appropriately communicates the scientific significance and value of all documents to the target audience, consistent with business processes and compliance requirements · Understand and use product strategy, communication objectives, and lexicon appropriately to ensure alignment with publication content · Maintain relationships with internal and external collaborators/authors on assigned documents and supports process improvement · Understand the publication landscape (e.g., journals, congresses, readership) and advise key stakeholders accordingly · Support documents and publication strategies and prioritization of documents and publications · Drive documentation project timelines and handle multiple projects at a time; may support one or more products · Ensure quality, alignment with objectives, and timely completion of publications while staying on track with allocated budgets · Draft and edit abstracts, posters, and slide decks for presentation at scientific and medical congresses. · Establish, maintain, and expand business relationships with cross-functional team members collaborating on publication projects to ensure accurate and timely completion/delivery of information based on publication plans. · Management of CRO medical writing relationship with regard to all protocol documents, FDA filings, and site communications like memos or addendums. · Maybe responsible for training, mentoring or supervising junior staff members · Other duties as assigned. REQUIRED EDUCATION & WORK EXPERIENCE: · Minimum Bachelor's Degree in a scientific field of study. Advance degree strongly preferred (MS, PhD, MD, PharmD, etc.). · Minimum 5+ years of direct scientific writing experience or 3+ years' experience with advanced degree. PREFERRED QUALIFICATIONS: · PhD, MD, or PharmD with at least 3-5 years of clinical documentation and publication development experience for industry in the bio-pharmaceutical sector · Experience preparing clinical research documents, and manuscripts for publication in peer-reviewed medical journals as well as abstracts and posters or oral presentations for scientific congresses · Experience working in a matrix team setting · Experience collaborating with clinical investigator authors/collaborators on documents and publication development · Exceptional analytical, communication, organizational, and interpersonal skills · Ability to apply project management skills to advance numerous projects at a time and to deliver high-quality documents rapidly · Ability to lead and/or facilitate effective team meetings for deliverables · Proficient in word processing and pertinent software (e.g., Microsoft Office, EndNote) · Knowledgeable about ICMJE (International Committee of Medical Journal Editors) and GPP3 · Good Publication Practices 3 guidelines FUNCTIONAL / TECHNICAL KNOWLEDGE & SKILLS: · Knowledge of cGMP requirements for pharma / biotech industry · Small molecule drug development · Regulatory environment · Process, procedures and best practices · Proficient in Microsoft Office (Word, Excel, and Power Point) and Smartsheet COMPETENCIES: · Attention to details · Collaborate · Communicate effectively in English, both oral and written · Deliver on commitments · Detail oriented and meticulous follow through · Maintain composure · Organizational skills · Proactively plan and organize · Solve problems · Adapt · Be self-aware · Manage and improve process · Facilitate · Influence and persuade · Lead
    $107k-154k yearly est.5d ago
  • TSSCI Tech Editor

    An employer is looking for multiple TS/SCI Technical Editors to sit onsite in Arlington, VA. Location: Arlington, Virginia- hybrid (2 days a week onsite)
    $52k-72k yearly est.5d ago
  • Proposal Strategist/Writer

    Formats responses into a professional template in alignment with Southern Scripts' brand standards. The Proposal Strategist/Writer manages high complexity weighted proposals. The Proposal Strategist/Writer works closely with leadership throughout Southern Scripts to create customized responses to RFx documents that differentiates Southern Scripts in the market, while developing strategic content tailored to the needs of clients. Submits proposals by the identified due date, coordinating the submission; proactively identifies, communicates, and develops risk mitigation plan to support revenue-generating proposals for Southern Scripts.
    $50k-80k yearly est.4d ago
  • Senior Medical Writer [REMOTE

    Principal Responsibilities: Write, edit, and manage documentation for regulatory submissions, such as protocols, synopses, INDs, and study reports. Write and edit other strategic documents as needed. Qualifications: Master's degree in life sciences or minimum 10 years of medical writing experience in the pharmaceutical industry. Excellent writing and communication skills. Proficient in interpersonal, organizational, and problem-solving abilities within a matrix management environment. Knowledge of FDA and ICH guidelines. Skilled in interpreting clinical data. Proven experience writing major documents (e.g., protocols, CSRs, ISE, ISS, Clinical Overviews). Familiarity with biopharmaceutical industry accounting, financial regulations, and tax laws. Experience with public company reporting and compliance requirements. Preferred Qualifications: Advanced Scientific Degree preferred with at least 8 years of relevant writing experience. Advanced knowledge of drug development and regulatory requirements for document organization. Project management experience, including negotiation and influence skills for timely, high-quality deliverables. Proven leadership in regulatory writing for INDs.
    $108k-142k yearly est.1d ago
  • Onsite Job - Technical Editor (Need Active Clearance TS/SCI CI Poly Required) - Reston Virginia

    Job Title: - Technical Editor Location - Reston Virginia
    $46k-62k yearly est.7d ago
  • Managing Editor of Content for

    Monster continues its pioneering work of transforming the recruiting industry We are looking for someone who thinks creatively but strategically, is eager to work collaboratively with our Managing Editor of News, and who has the drive to ensure our site continues to be the go-to resource for our military and veteran community. Join the team as our Managing Editor of Content! For more than 20 years, Monster has helped people improve their lives with better jobs, and employers find the best talent. Monster is a global leader in connecting people to jobs, wherever they are. Coordinating coverage and site operations while working closely and collaboratively with's Managing Editor of News to produce matching or supporting evergreen content
    $70.1k-145.7k yearly2d ago
  • Technical Editor - Mid Level

    SimVentions is a proud supporter of the U.S. military, and we take pride in our ability to provide relevant, game-changing solutions to our armed men and women around the world. SimVentions is about more than just being a place to work with other growth-orientated technically exceptional experts. At SimVentions, we don't just hire the smartest people. SimVentions, consistently voted one Virginia's Best Places to Work, is looking for a Mid-Level Tech Writer to join our team! SimVentions takes pride in its innovative and cutting-edge technology, so you can be sure that whatever project you work on, you will be having a direct impact on our customer's success.
    $52k-72k yearly est.1d ago
  • Managing Editor, Online Content

    Managing Editor, Online Content is a key member of our executive team and our market intelligence team.
    $51k-82k yearly est.5d ago
  • Senior Medical Writer - Medical Communications Agency - Remote

    I am excited to be partnered with a top client of mine on their search for a seasoned Senior Medical Writer to join their ever-growing team! As Senior Medical Writer - You will be the scientific client lead on your designated accounts and heavily involved in all scientific strategy initiatives. Builds strong client relationships - Starts to help shape client strategy, recommending new projects or advising when taking a different approach may better meet client objectives Ensure all deliverables are scientifically accurate, fully referenced, appropriate to the target audience, and consistently meet the highest quality standards
    $91k-136k yearly est.1d ago
  • Medical Writer

    The Medical Technical Writer serves as the interface between GMW and Global Regulatory Operations.
    $77k-106k yearly est.6d ago
  • Managing Editor

    The ideal candidate will have experience in the medical or scientific scholarly journal arena. Some necessary attributes for success here are excellent communication skills, being detail-oriented, a willingness to learn a new market, and faithfully executing daily tasks. This job can be done remotely and at mutually-agreeable hours. Remote work status is preferable, since our employees are spread across the country. We publish the only peer-reviewed medical journal in the US that reaches both clinicians and administrators at Urgent Care centers nationwide. JUCM: The Journal of Urgent Care Medicine is published monthly except for a combined July/August issue, so July would be a non-working and unpaid month. This is a high-profile job in this vertical market. This position reports directly to the publisher. Additional project work in urgent care is available, if desired, and is compensated separately on a project by project basis. This job is estimated to take 30 hours per week. Compensation of $6,300 per month, except July. Responsibilities Interface with authors, peer reviewers, publisher, clinical and practice-management editors. Maintain editorial pipeline documents Assure submissions adhere to our guidelines and are processed through existing editorial systems Oversee the creation of each issue in conjunction with the Art Director Assist with ongoing editorial projects Copyedit and proofread each issue Qualifications Bachelor's degree or equivalent experience Strong interpersonal and communication skills Experience in editing and managing a medical/scientific journal Proficient in Microsoft Office suite Detail-Oriented
    $6.3k monthly1d ago
  • Senior Technical Writer

    At Amador we provide global-standard translational sciences and clinical pharmacology services to biopharmaceutical companies in US, EU and China. Amador aims to become a leading global partner for the successful development of novel and improved biotherapeutics.
    $55k-72k yearly est.3d ago
  • Remote Medical Writer Opportunity

    Our client, a pharmaceutical manufacturing company that specializes in neuroscience is looking to bring on a Medical Writer IV to the team.
    $100 hourly1d ago
  • Senior Proposal Writer (Remote

    GovCIO is a team of transformers--people who are passionate about transforming government I.T.
    $71k-109k yearly est.6d ago
  • Sr. Writer/Editor for Healthcare/Medical Content

    *This job is fully remote and requires someone who can work fully on PST hours (8-5pm) *Requires 5 years of writing editing experience and someone who already has worked in healthcare / medical content. *Examples of your writing will be required as part of the submission/application process. Essential Functions: Employees must abide by all Joint Commission requirements including, but not limited to, sensitivity to cultural diversity, patient care, patients' rights and ethical treatment, safety and security of physical environments, emergency management, teamwork, respect for others, participation in ongoing education and training, communication and adherence to safety and quality programs, sustaining compliance with National Patient Safety Goals, and licensure and health screenings. Write, develop, copy, and edit patient education content with an emphasis on health literacy strategies. Guide the writing and content creation process, bringing projects from concept to completion and ensuring brief requirements and deadlines are met. Collaborate with the clinical team to assess and manage patient education requests. Ensure consistency of messaging and tone across all channels and touchpoints. Lead initiatives to update and enhance existing content. Mentor and support other writers, including providing guidance and direction to freelance writers and outside content vendors. Contribute solutions based on a solid understanding of best practices in health patient education, including how to structure and optimize content. Leverage research, insights, data and relevant trends to inform writing best practices and copy guidelines. Present creative and content choices confidently and have a point of view on best overall presentation and delivery of content. Manage multiple projects simultaneously in a fast-paced, dynamic environment. Build consensus and work effectively with all cross-functional team members, driving collaboration and continual improvement Requirements: BA or equivalent required, preferably in health sciences or health education Five (5+) years professional writing and editing experience Experience in the health education or communication field preferred. Be able to write in "plain language/health literacy" and be very comfortable in Microsoft Office applications. Experience with, and demonstrated understanding of, health care systems and content. Experience in translating complex medical information into plain language for patient information. Proven excellence in writing and editing. Thoughtful and strategic approach to problem solving Exceptional attention to editorial detail. Ability to manage multiple projects on short deadlines. Strong interpersonal skills, and ability to give and receive constructive editorial feedback. Understanding of content strategy and content management systems. Comfortable operating independently and collaboratively. Strong portfolio indicating versatility with examples of various forms of writing and approaches
    $100k-147k yearly est.6d ago
  • Sr Technical Writer

    Prepare, review, revise, and maintain documentation in the form of user guides, integration guides, developer guides, in-platform instructions, installation/configuration instructions, system operations, policies, and standards. Prepare, review, revise, and maintain end user resources and educational materials, including videos, demos, tutorials, training materials, in-depth user guides, general & technical overviews, FAQs, and in-product help documentation. Write, format, edit, review, and proof procedural and technical information for technical and nontechnical users
    $59k-82k yearly est.5d ago
  • Foundation Grant Writer

    AbleLight is currently seeking a Foundation Grant Writer. The Foundation Grant Writer will possess an ability to translate strategic programs, mission, and funding priorities to meet foundation funder guidelines and program priorities. The Foundation Grant Writer is responsible for writing all foundation or grant LOI's, grant applications, proposals, grant reports and conducting all grant program tracking, including managing proposal submission deadlines and deliverables. The Foundation Grant Writer applies knowledge of fundraising methods and plans to reach income goals and collaborates with team members in the organization to assist with other fundraising projects and develop relationships with key stakeholders. In this role, the Grant Writer is a key member of the development team and in collaboration with the VP of Strategic Support & Business Development, will build our foundation prospect pipeline to identify and secure new sources of revenue in support of our mission.
    $45k-62k yearly est.2d ago
  • Proposal Writer

    Location:McLean, Virginia, USA McLean , Virginia , USA
    $93k-129k yearly est.7d ago
  • Sr Technical Writer

    This role will function as a primary writer-responsible for deliverables of with varied scope and complexity. Location: Location: Charlottesville VA / 2 -3 days on site required initially (Local Preferred)
    $63k-84k yearly est.5d ago
  • Senior Technical Writer - Remote

    Where required by law, NTT DATA provides a reasonable range of compensation for specific roles. NTT DATA Services strives to hire exceptional, innovative and passionate individuals who want to grow with us. As part of NTT DATA, a $30 billion trusted global innovator with a combined global reach of over 80 countries, we help clients transform through business and technology consulting, industry and digital solutions, applications development and management, managed edge-to-cloud infrastructure services, BPO, systems integration and global data centers. NTT DATA is committed to complying with the Safer Federal Workforce Task Force COVID-19 Workplace Safety Guidance for Federal Contractors and Subcontractors to the extent it is enforced by the federal government or any of its clients. NTT DATA Services is a recognized leader in IT and business services, including cloud, data and applications, headquartered in Texas. We are currently seeking a Senior Technical Writer to join our team remotely in the United States.
    $61.8k-128.9k yearly6d ago

Proposal Writer Jobs FAQs

How Much Do Proposal Writers Make?

Proposal writers make an average of about $73,000 a year. However, this salary can vary greatly as the range is anywhere from $12,000 to $100,000 a year. This variation is largely due to factors such as differences in:

Is Proposal Writing A Good Career?

Yes, proposal writing is a good career. It pays well, and many people who do it feel very fulfilled. Proposal writing will improve your communication skills, help you learn a lot about your company and the industry within which you operate, and your work has the potential to make a real, tangible impact.

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