6 jobs found
- We are seeking a skilled and adaptable Medical Writer to join our growing team in Port St. Lucie, Florida! As a dynamic pharmaceutical communications agency, we develop innovative and compelling content for a variety of clients, ranging from established pharmaceutical giants to cutting-edge biotech startups. The Medical Writer will contribute to a diverse portfolio of projects, including clinical study reports, regulatory submissions, medical education materials, and publications. You will collaborate closely with cross-functional teams including physicians, scientists, and project managers. **What You'll Accomplish:** * Develop scientifically accurate and engaging medical content that adheres to industry guidelines and client requirements. * Research and synthesize complex clinical data to create clear, concise, and persuasive documents. * Collaborate with medical experts and key opinion leaders to ensure accuracy and relevance of content. * Manage multiple projects simultaneously while meeting deadlines and maintaining high-quality standards. * Stay abreast of current medical literature and industry trends to ensure content is cutting-edge and aligned with best practices. * Adapt your writing style to meet the unique needs of each project and target audience. **A Foundation for Success:** * A graduate degree in a relevant scientific discipline (e.g., biology, pharmacology, or related life science). * Demonstrated experience in medical writing, ideally within a pharmaceutical or agency setting. * Deep understanding of clinical research, regulatory requirements, and medical terminology. * Excellent communication, writing, and editing skills with meticulous attention to detail. * Ability to work independently and collaboratively within a fast-paced, team-oriented environment. * Proficiency in Microsoft Office Suite and other relevant software applications. **Beyond the Ordinary Perks:** * Competitive salary and benefits package, including comprehensive health insurance, generous paid time off, and a retirement plan. * Opportunity to work on diverse and challenging projects that contribute to advancements in healthcare. * Collaborative and supportive work environment that values innovation and continuous learning. * Professional growth and development opportunities, including training programs and conference attendance. * Flexibility to work remotely or in a hybrid work arrangement, offering work-life balance. **Our Commitment:** Our company values inclusivity, integrity, and innovation. We strive to foster a supportive and respectful workplace where every team member can thrive and contribute their unique skills and perspectives. If you're ready to apply your medical writing experience in a role where your talents are valued, please submit your resume and a brief cover letter.Port St. Lucie, FLRemote/HybridFull-time$60,000 - $85,000 per yearMedical Writing8 days ago
- We are a cutting-edge biotech company nestled in the heart of Baltimore, renowned for pioneering advancements in personalized medicine. We're currently seeking a highly skilled technical writer to bridge the gap between our complex research and the clinicians who rely on it. Your primary charge will involve translating dense scientific data into clear, concise, and accessible documentation. Think user manuals, training materials, API documentation, and detailed reports designed for healthcare professionals. Your days will be varied and challenging, including participating in project meetings with researchers, crafting technical documents, editing and revising content based on feedback, and collaborating with our regulatory affairs team to ensure all documentation meets compliance standards. A strong grasp of medical terminology is vital, and a knack for simplifying convoluted concepts is essential. We envision the ideal candidate as someone with a passion for precision, an insatiable curiosity for science, and an unwavering commitment to providing top-tier user experience. **Principal Duties** 1. Generate comprehensive user manuals and API documentation that serve as intuitive resources for clinicians, researchers, and internal teams. 2. Confer directly with subject matter experts—including researchers and product developers—to internalize the critical details required for each document's creation. 3. Assimilate clinical study results and transform them into accurate, understandable technical reports for external consumption. 4. Review existing material to enhance its clarity, cohesiveness, and accessibility, while maintaining strict standards of medical accuracy. 5. Actively participate in cross-functional team settings to provide insight during product design and user experience improvement phases. 6. Collaborate intimately with quality assurance divisions to enact thorough quality checks, identifying any inaccuracies that detract from the document's technical fidelity. **Attributes for Success** * Proven field experience in technical writing, particularly within the medical, pharmaceutical, or biotechnology sectors. * Exceptional fluency in industry-specific vernacular. * Evidence of scholarly preparation in scientific writing or a correlative technical field. * Keen aptitude for converting specialized terminology and challenging themes into approachable material. * Strong capacity for self-led enterprise, characterized by efficient task-handling and meeting targets in a fast-paced climate. * Acumen with standard software suites like Microsoft Office, as well as document layout and graphics incorporation platforms. **What Awaits You Here** * Comprehensive health benefits including dental and vision. * A generous paid time off program to maintain work/life equilibrium. * Ongoing opportunities for skill cultivation with paid workshops and courses. * Retirement funding with matching company assistance. * Collaborative workplace dedicated to driving developments in health tech. * Potential prospects for growth within the organization.Baltimore, MDHybrid / On-siteContractor$60,000 - $80,000 per yearTechnical & Medical Writing8 days ago
- The healthcare industry is experiencing rapid advancements in technology, demanding professionals who can effectively communicate complex information to diverse audiences. We are currently growing our technical documentation team and need a talented individual that can synthesize information and create clear, concise and easily accessible documents and guides. As our new hybrid Technical Writer in Cincinnati, OH, you'll transform sophisticated technical details into user-friendly documentation, playing a pivotal role in product adoption and satisfaction. **Crafting the User Experience Through Documentation** As a key contributor, you'll be diving deep into product functionalities to create comprehensive user manuals, API documentation, and troubleshooting guides. Your ability to translate technical jargon into accessible language will directly impact our users' experience and understanding. Collaborating closely with engineers, product managers, and customer support, you’ll ensure accuracy, clarity, and relevance across all documentation. **Key Responsibilities** * Produce detailed documentation including user guides, API references, and knowledge base articles. * Work with cross-functional teams to comprehend project needs and create supportive documentation. * Consistently refresh existing materials for relevance and efficacy. * Organize and manage project documentation libraries for convenient access. * Analyze customer comments to strengthen document usefulness and overall approval. * Employ illustrations, diagrams, animation, and charts to increase documentation effectiveness. * Participate in documentation tests, collect, assess and adjust the feedback. **Professional Skillset** * Background in technical writing with documented project management experience. * Superb ability to grasp intricate concepts and convey them simply and clearly. * Expert at various tech writing applications and project management tools. * Skill in collecting information from subject experts to support written explanation. * Prior engagement with software development lifecycle and its influence on documentation. * Familiarity with Agile process. * Familiarity with a variety of presentation methods, including graphics and video. **Elevating Your Career Here** We offer competitive compensation and a comprehensive benefits package designed to support your well-being and professional growth. These include but are not limited to flexible work options to enhance your work-life balance and continuous learning to stay ahead in the rapidly evolving field of health tech. Expect opportunities to develop through workshops, online courses and convention attendance. **Our Promise to Employees** We value diversity and actively nurture an inclusive work atmosphere that accepts different origins, viewpoints, skills, and experiences. Our dedication to equality is visible in our employee opportunities and advancement procedures. We actively encourage applicants from varied populations and promote accommodations in line with business procedures.Cincinnati, OHHybridFull-Time$65,000 - $85,000 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
- 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