168 jobs found
- We are looking for a tech-savvy and creative Technical Blog Writer to craft engaging and informative content about our cutting-edge technology and its applications. Our ideal candidate has a knack for taking complex technical jargon and making it accessible to a broader audience, especially potential clients in Tampa, FL. This is a unique opportunity to influence our brand voice and establish thought leadership in the tech space. We need a writer who understands the local landscape and can tailor content to resonate with Tampa's business community and its vibrant tech scene. **Your Mission:** * Create high-quality, SEO-optimized blog posts, white papers, and case studies about our software and services. * Collaborate with our product development and marketing teams to understand our products and their key benefits. * Transform technical specs and data into compelling stories that demonstrate the value of our solutions to potential clients. * Tailor content to the Tampa, FL market, including references to local industries and business trends. * Help grow our organic traffic and lead generation efforts through engaging content. **Attributes That Matter:** * A background that showcases experience as a technical writer, content creator, or blogger. * Proficiency in understanding and explaining complex technical concepts to non-technical audiences. * Proven success in producing high-quality content that drives engagement and conversions. * Excellent research and analytical abilities with focus on data gathering. * Knowledge of SEO best practices and keyword research for content optimization. **Tangible Skills** * Excellent writing, editing, and proofreading prowess. * Familiarity with content management systems (CMS) such as WordPress, Contentful and others. * Experience using SEO tools such as Google Analytics and Semrush. * Ability to work both independently and collaboratively in a fast-paced startup environment. * Understanding of HTML, CSS, and other web technologies. **Compensation & Perks** At [Company Name], we put team wellbeing first. As a full-time employee, you can expect: * A competitive compensation package that recognizes your expertise and contributions. * Health, dental, and vision coverage for you and your family. * Paid time off, including vacation, sick days, and holidays. * Opportunities for professional development and advancement within the company. * A collaborative and supportive work environment where you can make a real impact.Tampa, FLRemote/On-siteContractor$60,000 - $80,000 per yearTechnical Writing & Bloggingabout 1 month ago
- Our biotech company in San Francisco is on the hunt for a meticulous and innovative Medical Writer to join our growing team. We need a highly skilled communicator who can transform complex scientific data into easily digestible content for a variety of audiences, ranging from regulatory bodies and healthcare professionals to patients and the general public. This role is essential for our company's mission to improve patient outcomes through cutting-edge therapies. This is a full-time, on-site position with opportunities for remote work. **Key Responsibilities:** * **Regulatory Writing Expertise:** Develop and maintain clinical study reports (CSRs), investigator brochures (IBs), and other regulatory documents. Ensure all materials are compliant with FDA and international guidelines. * **Publication Planning and Execution:** Participate in the planning and execution of scientific publications, including peer-reviewed articles, abstracts, and poster presentations. Collaborate with researchers and medical affairs professionals to generate high-quality publications. * **Medical Communications Content Creation:** Create a range of medical communication materials, such as slide decks, training modules, and educational resources for healthcare providers. Tailor content to meet the specific needs of different audiences. * **Literature Reviews and Data Synthesis:** Conduct thorough literature reviews and synthesize complex data from clinical trials and other sources. Translate data into clear, concise, and accurate written materials. * **Collaboration and Teamwork:** Work closely with cross-functional teams, including clinical development, medical affairs, and marketing. Contribute to the development of overall medical communication strategies. * **Maintain Current Knowledge:** Stay up-to-date with current medical literature, regulatory guidelines, and industry trends. Apply this knowledge to the development of innovative and effective medical writing solutions. * **Quality Control:** Ensure accuracy and consistency of all written materials through rigorous review and editing processes. **Essential Qualifications:** * A relevant scientific background, ideally in biology, pharmacology, or a related field. * Proven capability in crafting regulatory documents, such as clinical study reports, investigator brochures, and safety updates. * In-depth grasp of clinical trial designs, statistical analyses, and medical terminology. * Fluency in regulations concerning medical writing and publishing ethics (ICH guidelines, GPP, etc.). * Impeccable written and oral communication competencies. * A commitment to excellence, accuracy, and scrupulousness in all aspects of medical writing. **What We Offer:** * A competitive salary with performance-based bonuses. * Complete health, dental, and vision coverage. * Generous paid time off (PTO) and company holidays. * A 401(k) plan with employer matching. * Proficient growth potential within the company. * Engaging in projects and initiatives with real-world impact. * A positive, diverse, and inclusive work environment. We embrace new ideas and strive for continuous growth. If you possess a passion for medical communication and aspire to make a tangible difference in healthcare, we encourage you to apply. Your skill and dedication will play a crucial role in our mission to drive forward advancements in medicine.San Francisco, CAOn-site/RemoteFull-time/Contractor$90,000 - $130,000 per yearMedical Writingabout 1 month ago
- Our innovative biotech firm is seeking a skilled Technical Documentation Specialist in the heart of San Francisco's vibrant innovation district. This individual will be instrumental in crafting comprehensive and user-friendly documentation for our cutting-edge scientific products. Our ideal candidate has a strong understanding of scientific principles and an innate ability to translate complex concepts into clear, concise, and accessible information for a wide range of audiences. The role will sit onsite. **Your Daily Bread (and Butter):** * Develop and maintain detailed technical documentation, including user manuals, API documentation, training materials, and troubleshooting guides. * Collaborate closely with scientists, engineers, and product managers to gather information and ensure accuracy of content. * Create visually engaging graphics, diagrams, and flowcharts to enhance understanding and usability of documentation. * Manage the documentation review process, incorporating feedback from subject matter experts and end-users. * Implement and maintain documentation standards and style guides. * Contribute to the development and maintenance of our internal knowledge base. * Participate in the development and execution of documentation plans for new products. * Ensure all documentation adheres to regulatory requirements. * Actively seek opportunities to improve documentation processes and workflows. * Stay current with industry best practices and trends in technical communication. **What You Should Bring to the Table:** * A bachelor's degree in a scientific field, technical communication, or a related discipline. Advanced degrees a definite plus. * Demonstrated professional journey in technical writing, with a focus on scientific or technical products. * Practical mastery of documentation tools and technologies, such as MadCap Flare, Adobe FrameMaker, or similar. * Exceptional written and verbal communication skills. * Proven ability to work collaboratively in a fast-paced, cross-functional environment. * Detail-oriented with a strong focus on accuracy and consistency. * A passion for simplifying complex information and improving user experience. * Familiarity with regulatory requirements for scientific documentation. **The Perks of Working with Us:** We pride ourselves on our dynamic, inclusive culture, and reward ingenuity with outstanding benefits including: * Comprehensive health, dental, and vision insurance. * Generous paid time off and holidays. * A chance to contribute to a transformative business! * Company-sponsored professional development opportunities. * Stock options. * Employee assistance program. As a Technical Documentation Specialist at our San Francisco facility, your skills will directly impact how our breakthrough science is understood and implemented. If you thrive in a collaborative, fast-paced environment, and possess an exceptional knack for explaining the complex, we strongly urge you to apply today!San Francisco, CAOn-siteFull-time$90,000 - $120,000 per yearTechnical Writingabout 1 month ago
- Our team at Innovatech Solutions, a cutting-edge tech firm in Jersey City, NJ, seeks a meticulous and detail-oriented Technical Writer to create clear and concise documentation for our groundbreaking software. We're not just another software company; we're architects of future technologies, located a stone's throw away from NYC's bustling tech scene, but with our own unique vibe. As a Technical Writer at Innovatech, you will be responsible for developing and maintaining various types of technical documentation, including user manuals, API documentation, release notes, and troubleshooting guides. You will collaborate closely with our engineering, product, and support teams to ensure accuracy, clarity, and completeness of all documentation. **Key Responsibilities:** * Produce top-tier, easy-to-understand documentation for both technical and non-technical audiences. * Maintain an intimate knowledge of our software's functionality and architecture. * Collaborate seamlessly with engineers, product managers, and customer support to gather information. * Ensure adherence to our internal documentation standards and style guides. * Participate actively in the planning and design phases of new features to ensure documentation needs are addressed early. * Keep all documentation up-to-date, reflecting changes in our rapidly evolving product. * Explore and recommend innovative documentation methods and technologies to optimize the user experience. **What Makes You an Ideal Candidate:** * Proven skills in crafting technical documentation within a software development setting. * Exceptional written and verbal communication abilities; must be a master of clarity. * A solid grasp of software development methodologies and practices. * Competence in using documentation tools and platforms, such as Confluence, Markdown, or similar technologies. * A collaborative mindset with the ability to work across multiple teams and disciplines. * Experience working in an Agile development environment is advantageous. * A passion for continuous learning and keeping pace with the newest technologies. **Benefits of Joining Innovatech:** * Competitive salary and comprehensive benefits package including medical, dental, and vision coverage. * Generous paid time off and holidays, because we recognize the importance of work-life harmony. * Professional development opportunities to enhance your technical writing expertise. We invest in our people. * Stock options, as we believe in sharing our success with those who contribute. * A collaborative and engaging work environment, where your ideas are heard and valued. Enjoy coming to work. * Convenient location in Jersey City, with easy access to public transportation, and a thriving downtown. * Remote work possibility offering flexibility to structure your work environment around personal needs and location, as we embrace a healthy work-life mix. Innovatech Solutions provides equal opportunities for all and prioritizes establishing a varied personnel. People from all groups are welcome to apply for employment with us. Embark on this incredible path toward professional and personal accomplishment.Jersey City, NJRemoteFull-time$80,000 - $100,000 yearlyTechnicalabout 1 month ago
- We're seeking a detail-oriented and highly skilled Medical Writer to join our growing team in Frisco, TX. In this hybrid role, you'll primarily be working remotely, with occasional in-office days for team collaboration and meetings. The Medical Writer will be responsible for creating accurate, informative, and engaging content related to medical devices, pharmaceuticals, and healthcare topics. Your contributions will support marketing initiatives, educational programs, and regulatory submissions. **Responsibilities of the Position** * Research and write comprehensive documents, including clinical study reports, regulatory documents, white papers, abstracts, posters, presentations, and journal articles. * Collaborate with subject matter experts, including physicians, scientists, and marketing professionals, to gather information and ensure accuracy of content. * Interpret scientific data and translate complex information into clear and concise language suitable for target audiences. * Maintain up-to-date knowledge of industry trends, regulatory guidelines, and medical advancements. * Manage multiple projects simultaneously, adhering to timelines and budget constraints. * Ensure all content is compliant with regulatory requirements and ethical guidelines. * Develop and maintain a thorough understanding of therapeutic areas and product lines. * Participate in the development of medical communication strategies. * Review and edit content for accuracy, clarity, and consistency. **What You Need to Succeed** * Advanced academic background in a scientific field such as biology, chemistry, or medicine. A Master’s degree is strongly preferred. * Proven professional journey of 3+ years of experience in medical writing, with a focus on regulatory documents. * Exceptional writing, editing, and proofreading abilities, with a keen eye for detail. * Deep understanding of medical terminology, clinical research, and statistical concepts. * Familiarity with FDA guidelines, ICH guidelines, and other relevant regulations. * Proficiency in Microsoft Office Suite and document management systems. * Excellent communication and collaboration skills, with the ability to work effectively in a team environment. * Ability to interpret complex data and present it in a clear and concise manner. * Solid organization skills and ability to manage multiple projects simultaneously. **Our Commitment to You** We provide a supportive and collaborative work environment that fosters growth and development. Benefits encompass: * Competitive base salary and performance-based incentives. * Comprehensive health, dental, and vision insurance plans. * Generous paid time off, including vacation, sick leave, and holidays. * 401(k) retirement plan with company matching contributions. * Professional development opportunities, including training programs and conference attendance. * Hybrid work arrangement offering flexibility and work-life balance. * Employee assistance program providing confidential counseling and support services. * Opportunity to work on challenging and impactful projects. * Collaborative and supportive team environment. * Company events and team-building activities.Frisco, TXRemote/HybridFull-time$70,000 - $95,000 per yearMedical Writingabout 1 month ago