6 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 organization needs a dynamic medical writer to support our expanding research initiatives based in Portland, Oregon. This is a freelance, remote-eligible opportunity, designed for a detail-oriented individual with an affinity for scientific communication. The core focus will be creating clinical reports, regulatory submissions, and publication materials, ensuring accuracy and clarity across all outputs. **Your Impactful Role** As a medical writer, your primary functions include researching complex clinical data, transforming findings into accessible scientific content, and contributing to strategic publication planning. Key tasks entail: 1. Composing scientifically sound clinical study reports that meet regulatory standards. 2. Crafting manuscripts and abstracts for publication in peer-reviewed journals. 3. Developing engaging presentations for medical conferences and internal educational purposes. 4. Assisting in the creation and execution of medical communication strategies in coordination with medical affairs. 5. Collaborating closely with cross-functional teams including clinicians, biostatisticians, and regulatory affairs specialists. 6. Maintaining up-to-date awareness of industry trends and regulatory guidelines pertinent to medical writing. **Essential Mastery and Capabilities** Candidates must possess: * A master’s degree in life sciences, pharmacology, or a related field. * Established industry background, specifically in medical writing within a pharmaceutical, biotech, or CRO environment. Experience that involves more than two years in this specific domain will significantly impact the success. * Detailed grasp of medical terminology, statistical principles, and clinical trial design. * Competency in producing documents compliant with ICH guidelines and other regulatory norms. * Superior capabilities in analytical thinking, writing, and communication, suited to crafting impactful scientific narratives. * High degree of proficiency using document management and publishing software. * You’re probably the type who has great attention to detail and meticulousness. It is expected from our candidates that they manage their time and prioritize projects efficiently to adhere to project milestones and deadlines. **Total Rewards for Your Contributions** We prioritize the health and well-being of our team. For this freelance opportunity, we offer: * Competitive project-based compensation. Also included, is flexibility to tailor projects according to expertise and availability. * Opportunities for skill cultivation and continuous professional evolution. Also offered are chances to access workshops and resources that nurture growth and enrich capabilities. * Impactful involvement in influential clinical research. The reward of shaping impactful narratives in the healthcare domain also awaits the talented candidate. * A supportive team culture where your contributions are valued. An environment fostering creativity and innovation is very conducive to development and is offered to the selected professional. **Agency Culture** Located in the vibrant creative hub of Portland, our agency offers a dynamic work environment that cherishes individual contributions. If you thrive in a collaborative and innovative space where the emphasis lies on achieving medical communication excellence, we encourage your application. We are keen to welcome talent that contributes toward advancing healthcare narrative through meticulously crafted and scientifically sound documents.Portland, OROn-site/RemoteFreelance$45-$65 per hourMedical & Web Content Writing20 days ago