14 jobs found
- We are looking for a sharp technical writer to bolster our growing documentation team. Our software, used by medical professionals across the country, is becoming increasingly complex, and we need someone who can translate intricate processes into simple, easy-to-understand user guides, API documentation, and troubleshooting manuals. As our technical writer in Minneapolis, you'll be instrumental in improving user experience and reducing support requests. **Responsibilities Include:** * Authoring, editing, and maintaining technical documentation, including user manuals, API guides, and release notes. * Collaborating with software engineers, product managers, and support teams to understand product functionality and translate it into clear, concise documentation. * Conducting thorough research on technical topics to ensure accuracy and completeness of documentation. * Creating diagrams, illustrations, and other visual aids to enhance understanding. * Ensuring documentation is consistent with company branding and style guidelines. * Managing documentation repositories and version control. * Identifying and addressing gaps in existing documentation. * Participating in documentation review cycles and incorporating feedback. * Staying up-to-date with industry trends in technical communication. * Optimizing documentation for search engine discoverability. **Skill Cultivation & Background:** * A minimum of 3 years of professional journey as a technical writer or similar role. * Superb writing, editing, and proofreading proficiencies. * Familiarity with software development lifecycles and agile methodologies. * Hands-on expertise with documentation tools, such as MadCap Flare, Confluence, or similar. * Practical knowledge of API documentation and related technologies (REST, JSON). * Working history with version control systems (Git). * Capacity to comprehend complex technical concepts and translate them into understandable language. * Intellectual foundation: Bachelor’s degree in technical communication, English, computer science, or a related field. * Bonus: Skill cultivation with video creation and editing. **What We Bring to the Table:** As a rapidly expanding software company deeply embedded in Minneapolis's growing tech sector, we believe in offering a robust and comprehensive compensation package. We provide competitive pay commensurate with experience and proficiency. Besides that, we believe in an inclusive culture fostering growth: * Health insurance: Comprehensive medical, dental, and vision plans available from day one. * Time Off: Generous paid time off policy, encompassing vacation, sick leave, and personal days. * Learning fund: budget for conferences and courses. * 401(k) plan: Contribute to our company supported 401k * Company events: Regular team-building activities and social events in Minneapolis. * Public transport benefits: For onsite workers, we offer a monthly metro pass. * Onsite Perks (if applicable): free coffee from a local Minneapolis roasterMinneapolis, MNOn-site, RemoteFull-time$70,000 - $90,000 per yearTechnical, Medical12 days ago
- Join our cutting-edge pharmaceutical company as a Medical Device Technical Writer in North Las Vegas, NV. This hybrid role blends the precision of technical writing with the dynamic requirements of the medical device industry. We're not just crafting documents; we're shaping user experiences and ensuring patient safety through clear, concise, and accessible technical information. **Your Daily Creations** * Author, revise, and maintain technical documentation for a range of medical devices, encompassing user manuals, installation guides, maintenance procedures, and troubleshooting guides. * Collaborate with engineers, product managers, and regulatory affairs specialists to capture the nuances of device functionality and regulatory prerequisites. * Organize and articulate complicated technical concepts into easy-to-understand language for both technical and non-technical audiences. * Ensure compliance with industry standards and regulatory guidelines (e.g., FDA, ISO) in all documentation. * Manage the documentation lifecycle, including planning, writing, editing, and version control. * Participate in usability testing to enhance the clarity and effectiveness of documentation. * Contribute to the development and refinement of our document control processes. * Proofread and edit documentation created by other team members. * Spearhead documentation updates in response to device modifications, software updates, or feedback from the field. * Craft visual aids such as diagrams, illustrations, and flowcharts to supplement written content. **Competencies That Matter** * Academic grounding in technical communication, engineering, or a closely allied discipline. * Established experience in technical writing within the medical device or pharmaceutical sectors. * Proficiency in documentation software and content management systems. * Profound understanding of regulatory necessities related to medical device documentation. * Demonstrated talent for grasping intricate technical subject matter. * Exceptional written and verbal communication prowess. * Detail-oriented work ethic with unwavering accuracy. * Team spirit combined with individual drive to satisfy deadlines. * An interest in novel medical technologies and the evolving regulatory milieu. **Rewards & Wellbeing** We deliver a competitive compensation package commensurate with expertise. Our total rewards program offers comprehensive medical, dental, and vision coverage, ample paid time off, a 401(k) plan with corporate contribution, and diverse wellness offerings. Additional benefits include professional development stipends and opportunities for career growth. **Company Culture & Perspective** We nurture a culture of cooperation, transparency, and incessant learning. Our team is united by a passion for impactful innovation and an unyielding commitment to patient-centric solutions. We celebrate originality and empower team members to push boundaries. Join us and contribute to enhancing the health and well-being of individuals globally.North Las Vegas, NVHybridFull-time$80,000 - $100,000 per yearMedical & Technical15 days 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 Writing17 days 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 Writing19 days ago
- Our growing medical communications agency needs a detail-oriented and imaginative medical writer near Anaheim, CA, to develop compelling content across various platforms. If you possess a knack for distilling complex scientific data into easily digestible, engaging narratives, we want to hear from you! **Crafting Clinical Narratives for Tomorrow** This role offers an extraordinary opportunity to translate intricate medical information into clear and captivating content for both healthcare professionals and the general public. You'll play a pivotal role in shaping effective communications strategies that help our clients navigate the ever-evolving landscape of medical research and treatment. Your passion for accuracy and storytelling will directly influence patient care and medical innovation. **Key Responsibilities Include:** * **Content Architect**: Conceptualize, research, and draft diverse medical communications materials, including manuscripts, abstracts, posters, presentations, and website content. Think journal articles, conference summaries, and educational resources. * **Precisionist**: Ensure content is scientifically accurate, compliant with regulatory guidelines, and aligned with client objectives. Scrutinize data and adhere to strict quality standards. * **Story Weaver**: Develop engaging and accessible narratives that resonate with target audiences. Create compelling stories that make an impact and drive results. * **Collaborative Catalyst**: Work closely with internal teams, clients, and key opinion leaders to gather information, align strategies, and refine content. Foster effective partnerships. * **Insight Miner**: Conduct comprehensive literature reviews and stay abreast of current medical research and industry trends. Maintain up-to-date knowledge. **Credentials that Inspire Confidence:** * Advanced scientific training, like a Master's degree in life sciences, pharmacology, or a related field. (PharmD, PhD preferred.) * Proven track record in medical writing within an agency or pharmaceutical setting. Prior exposure is a plus. * Expertise in AMA style guidelines. Proficiency with medical terminology. * Ability to interpret and summarize complex statistical data with precision. * Exemplary communication, writing, and presentation aptitude. Communicate your vision effectively. * Capacity to effectively manage projects and prioritize tasks in a deadline-driven environment. Self-direction needed! **Agency Advantages** * Competitive remuneration package with comprehensive benefits: Health, dental, and vision. * Generous vacation policies. * Professional advancement support including conference travel. * A vibrant, creative, and collaborative workspace. * Opportunity to create meaningful work that advances medical understanding. Join the cause. **Thrive With Us** Our mission is to promote healthier living through impactful communications. If you're ready to take on stimulating new tasks in medical communications and demonstrate expertise through excellent clinical content, reach out!Anaheim, CAOn-siteFull-time$70,000 - $90,000 per yearMedical Writing, Web Content19 days ago