5 jobs found
- We're an established biotech firm poised for a dynamic content transformation. We require a Medical Writer who thrives in a fast-paced, regulated environment. This role will shape the narrative of our innovative therapies and contribute significantly to patient outcomes in the Chula Vista area. Join us, and your pen will impact lives. **Your Core Focus** * Generate high-quality scientific content including clinical study reports, investigator brochures, and regulatory submissions. * Develop compelling medical education materials for healthcare professionals and patient advocacy groups. * Collaborate across teams – clinical, medical affairs, regulatory – ensuring alignment with overall communications strategies. * Stay current on therapeutic area landscapes, scientific advancements, and evolving regulatory guidelines. * Interpret complex clinical data and translate into clear, concise messaging for diverse audiences. * Uphold the highest standards of data integrity and compliance throughout content creation. * Champion consistent brand messaging in all external and internal medical communications. * Engage with key opinion leaders and medical experts to incorporate insights into communication strategies. * Review and revise content from other team members, providing constructive feedback. * Adapt messaging for global markets, considering cultural nuances and regulatory requirements. **What Makes You a Great Fit** The successful candidate will demonstrate: * An advanced degree in a scientific or medical field (PharmD, PhD, MD). * Proven track record in medical writing with direct experience in regulatory submissions. * Deep comprehension of clinical trial design, statistical data, and medical terminology. * Exceptional writing skills, with a knack for making technical information understandable. * Demonstrated project management capabilities with a keen ability to meet deadlines. * Excellent communication and collaboration skills for interfacing with various internal and external stakeholders. * An unwavering commitment to ethical conduct and data accuracy. * A robust portfolio displaying medical writing capabilities across a range of therapeutic areas. * A strong grasp of FDA regulations and industry best practices. * Familiarity with electronic document management systems (EDMS) and publishing processes. **Institutional Benefits** At [Fictional Biotech Company], we understand that our greatest assets are our people. We offer a comprehensive benefits package to support professional development, work/life balance, and overall well-being. Scholarly advancement is essential to our institution. We present: * Competitive salary and performance-based bonus incentives. * Full medical, dental, and vision coverage. * Generous paid time off and flexible work arrangements. * 401(k) plan with employer matching contribution. * Professional development funds for conferences, workshops, and certifications. * Access to a robust internal learning management system with skill-enhancement courses. * Wellness programs to promote physical and mental health. * Employee assistance program (EAP) for confidential counseling and support. * Opportunities for career growth and advancement within a leading biotechnology company. * Commitment to equal opportunity and diversity. * A supportive academic environment fostering collaboration and innovation. Our campus rests just a few miles from Otay Lake. We maintain a highly-ethical organization where your contributions translate directly to innovations across the medical landscape. If you're ready to make a difference with the written word, we invite you to apply. We can hardly wait to bring your enthusiasm to the team!Chula Vista, CARemoteFull-time / Contractor$80,000 - $120,000 yearlyMedical Writing / Content Marketing8 days ago
- Our team in San Jose, CA is seeking a dedicated Medical Writer to craft clear, concise, and compliant documentation across a variety of therapeutic areas. If you possess a strong scientific acumen and a knack for translating complex data into accessible language, this remote opportunity may be your next career milestone. **What You'll Contribute** * Author and edit clinical study reports, investigator brochures, and regulatory submissions. * Develop compelling marketing materials, slide decks, and abstracts for scientific conferences. * Collaborate with cross-functional teams including clinical development, medical affairs, and regulatory affairs. * Ensure documents are in line with FDA guidelines and industry best practices. * Participate in the literature review process and maintain current knowledge of relevant medical advancements. * Manage multiple projects and meet tight deadlines in a fast-paced setting. * Provide quality control review of documents prepared by other medical writers. **Necessary Abilities** * A graduate degree in a life sciences discipline (PharmD, PhD, MD, or equivalent) provides the necessary scholarly preparation. * Proven success in medical writing, including regulatory documents and publications provides the necessary hands-on expertise. * Familiarity with ICH guidelines and other regulatory requirements are also important. * A talent for writing, editing, and proofreading detailed technical content demonstrates important communication skills. * Capacity to interpret statistical data and present them in an engaging manner is necessary for success. * Excellent project management and time-management skills. * Experience with electronic document management systems. **Reasons to Work With Us** * Competitive compensation with performance-based bonuses. * Generous paid time off and comprehensive health benefits. * Work-from-home flexibility offering an ideal balance. * Opportunities for professional growth and continuing education. * Collaborative and inclusive work environment supporting work-life balance. * Access to cutting-edge technology and resources. * Be a part of a meaningful mission that helps to improve the health of patients. **Bonus Traits** * Experience with a specific therapeutic area. * A good track record of publishing scientific manuscripts. * Membership in professional medical writing organizations. * Proficiency in multiple software applications utilized in medical writing.San Jose, CARemoteFull-time, Contractor$90,000 - $140,000 yearlyMedical Writing19 days ago
- Our San Diego-based biotech firm is searching for a meticulous and imaginative technical writer to join our growing research and development division. As a contractor, you'll work directly with scientists, engineers, and software developers to create crystal-clear documentation, user manuals, and API references. You'll not only be explaining cutting-edge science but also streamlining workflows through superior technical communication. **Responsibilities Include:** * Collaborate with subject matter specialists to comprehend complex technical concepts. * Write, edit, and revise technical documentation such as user guides, API documentation, training materials, and standard operating procedures (SOPs). * Produce high-quality diagrams, charts, and illustrations to enhance written content. * Ensure documentation adheres to industry standards and regulatory guidelines (e.g., FDA, HIPAA). * Participate in document review cycles and integrate feedback from diverse teams. * Maintain a central repository of documentation, keeping it organized, accessible, and current. * Explore innovative methods to present information, including video tutorials or interactive simulations. * Contribute to the style guide, improving clarity and consistency across all documents. **You’re the Right Fit If:** * You hold a bachelor's degree in a scientific discipline (biology, chemistry, engineering, etc.) * You have a proven history of 3+ years in technical writing, ideally in the biotechnology or pharmaceutical domain. * You have experience documenting software applications and APIs. * You have a high proficiency with technical writing tools (e.g., MadCap Flare, Adobe FrameMaker, or similar). * You are able to analyze data, procedures, and other documentation to define problems with detailed written summaries. * You possess exceptional writing, editing, and proofreading skills, with a laser focus on accuracy and clarity. * You thrive in a collaborative environment and can work autonomously to deliver projects on time. * You're comfortable balancing multiple tasks and adapting to changing priorities. **Perks for Our Contract Technical Writer:** * Competitive hourly rate, commensurate with expertise. * Remote work setup flexibility (option for occasional on-site work in San Diego). * Opportunity to expand your skill-set within the fast-moving biotech field. * Access to our company’s libraries and technical resources. * Possibility of conversion to a full-time role upon completion of successful contracts. * Be part of an impactful team focused on developing revolutionary scientific discoveries for the world.San Diego, CARemote / On-siteContractor$40 - $65 per hourTechnical & Medical20 days ago
- Our growing pharmaceutical client in Port St. Lucie, FL is seeking a meticulous and adaptable Medical Writer to join their dynamic team. This is a unique opportunity to contribute to the development of vital medical communications materials across a variety of therapeutic areas. We are seeking a professional who thrives in both hybrid and remote environments and who can seamlessly adapt to the ever-evolving demands of the medical writing landscape. If you have a solid understanding of medical terminology, strong attention to detail, and a passion for clear and concise scientific communication, we want to hear from you! **Core Responsibilities:** * **Manuscript Development**: Craft, edit, and finalize scientific manuscripts for submission to peer-reviewed journals, ensuring alignment with all regulatory guidelines and internal style guides. * **Abstract & Poster Creation:** Develop compelling abstracts and visually appealing posters for presentation at scientific conferences. Leverage strong data interpretation skills to present findings accurately and engagingly. * **Medical Communication**: Develop a diverse array of medical communications materials, including slide decks, advisory board summaries, and educational resources for healthcare professionals. * **Regulatory Documentation:** Assist in preparing and reviewing regulatory documents, such as clinical study reports and safety summaries, ensuring accuracy, completeness, and adherence to applicable regulations. * **Literature Reviews**: Conduct comprehensive literature reviews to gather relevant scientific data, support the development of scientific content, and identify key trends within specific therapeutic areas. * **Collaboration**: Collaborate effectively with cross-functional teams, including medical directors, clinical scientists, and publication managers, to ensure alignment on project goals and objectives. * **Style Guide Adherence:** Maintain consistency in style and formatting across all documents, following established style guides and editorial processes. **Academic Qualifications:** * Bachelor's degree in a scientific discipline (e.g., biology, chemistry, pharmacy). A master's or doctoral degree is a plus. * Strong understanding of medical terminology, clinical research principles, and regulatory guidelines. * A minimum of 2 years of hands-on expertise in medical writing within the pharmaceutical industry, medical communications agency, or related field. * Exceptional writing, editing, and proofreading prowess with a keen eye for detail. * Proficiency in utilizing medical writing software and referencing tools. * Strong project management prowess and ability to manage multiple projects concurrently while meeting deadlines. * Excellent communication, interpersonal, and collaborative capabilities. **Team Advantages** We foster a supportive and growth-oriented studio culture. Team members gain substantial exposure to a broad range of projects, contributing significantly to our client's success. Our commitment to your career includes: * **Competitive contractor or full-time salary**: A compensation structure designed to value your contribution and attract top talent. * **Comprehensive Healthcare benefits**: Access premium medical, dental, and vision plans. Peace of mind is our priority. * **Flexible work arrangements**: Our team is designed to give you freedom; Choose the optimal mix of remote and in-office time in Port St. Lucie to maximize productivity and inspiration. * **Professional development funding**: Boost your proficiency and industry knowledge. We're here for your goals! * **Paid time off & Holidays**: We understand how crucial downtime is. Recharge! * **Collaborative environment**: Thrive in our supportive and innovative atmosphere, surrounded by like-minded experts who are passionate about science and communication.Port St. Lucie, FLHybrid / RemoteContractor / Full-time$60,000 - $90,000 per year (Full-time) $50 - $75 per hour (Contractor)Medical Writing20 days ago
- Our expanding research division seeks a skilled medical writer in Irvine, CA to create compelling and accurate medical communications. We're a growing firm dedicated to clear, evidence-based reporting for healthcare professionals and the public. If you have a knack for simplifying complex medical information, this freelance, on-site contractor role might be perfect for you. **Your Core Mission** * Craft detailed reports on clinical trials, adhering to stringent regulatory guidelines. * Develop informative content for patient education programs, ensuring accessibility and understanding. * Generate abstracts and manuscripts for peer-reviewed publications, contributing to the medical community. * Collaborate with physicians and scientists to translate complex research data into clear narratives. * Maintain comprehensive knowledge of medical terminology and regulatory compliance standards. * Assist with the development of marketing materials, presentations, and other communication tools. * Participate in quality control reviews to ensure accuracy and consistency of information. * Stay updated on current medical literature and industry developments, continually enhancing subject matter expertise. * Convert detailed scientific content into engaging visual resources such as charts and graphics to maximize audience accessibility and comprehension. * Regularly engage with project stakeholders, providing ongoing updates and proactively addressing potential challenges to maintain timelines and scope requirements. **Necessary Professional Background** * Advanced degree in life sciences, pharmacology, or a related medical discipline; a doctoral degree is extremely helpful. * Proven track record of medical writing within a pharmaceutical, biotech, or medical device environment; we would like to see your work. * Exceptional written communication abilities, demonstrated through sample reports and publications. * Strong understanding of FDA regulations and ICH guidelines concerning medical communications. * Experience interpreting and presenting statistical data within clinical reports. * Proficiency with medical writing software and citation management tools. * Exceptional attention to detail and commitment to producing high-quality, accurate content. * Demonstrated ability to collaborate effectively within cross-functional teams. * In-depth grasp of scientific research methodology, enabling sound analytical evaluation of data and thorough comprehension of complex research articles. * Superior project management expertise, ensuring the consistent fulfillment of project milestones and stringent adherence to regulatory criteria within specified schedules. **Benefits of Involvement** As a freelance contractor with our company, you'll gain exposure to a dynamic and rapidly evolving research environment. We prioritize professional growth, providing opportunities for continuing education and skill development in the expanding medical writing field. As we are a small company, you have an outsized opportunity to learn and make a difference. We also provide flexible work schedules, allowing contractors to balance project commitments with personal obligations. This promotes a good balance of work life and personal fulfillment, increasing work output overall.Irvine, CAOn-siteFreelance/Contractor$60 - $85 per hourMedical Writing26 days ago