10 jobs found
- Our medical communications agency, situated a stone's throw from the vibrant energy of Jersey City, is seeking a skilled freelance Medical Writer to bolster our growing team. We specialize in developing impactful, evidence-based scientific content for pharmaceutical and biotech clients. If you're adept at translating complex scientific data into compelling narratives and possess a strong understanding of clinical research, we'd love to hear from you. **Responsibilities Include:** * Crafting various medical communication deliverables such as manuscripts, abstracts, posters, presentations, and slide decks, tailored to diverse audiences (healthcare professionals, researchers, and patients). * Conducting thorough literature reviews and analyzing clinical trial data to inform the development of scientifically accurate and strategically sound content. * Collaborating closely with medical affairs teams, clinicians, and other stakeholders to understand their objectives and ensure alignment with strategic goals. * Ensuring all deliverables adhere to industry guidelines (e.g., GPP3) and regulatory requirements. * Managing multiple projects simultaneously, meeting deadlines, and maintaining high-quality standards. **Your Professional Profile Should Include:** * An advanced degree (PharmD, PhD, MD, or Master's) in a scientific discipline (e.g., biology, pharmacology, or related field). * Demonstrated professional journey as a Medical Writer, preferably within a medical communications agency or pharmaceutical company. * Exceptional writing, editing, and proofreading abilities, with a keen eye for detail. * Deep understanding of clinical research methodologies, statistical analysis, and medical terminology. * Excellent communication and interpersonal prowess, with the aptitude to work effectively in a collaborative environment. * Proficiency in using Microsoft Office Suite and other relevant software applications. **Standout Attributes Include:** * A passion for translating complex scientific concepts into clear and concise messaging. * An independent spirit, with the capacity to manage projects autonomously and meet tight timelines. * A commitment to maintaining the highest standards of scientific integrity and ethical conduct. * A proactive mindset, with a thirst for continuous learning and professional development. * Familiarity with the local healthcare landscape in the Jersey City/New York metropolitan area is a definite plus. **What We Offer:** * Competitive freelance rates commensurate with experience and project scope. * A flexible remote work environment that values work-life harmony. * The opportunity to work on a diverse range of medical communication projects, spanning various therapeutic areas. * Collaborative and supportive team environment with ample opportunities for learning and growth. * Exposure to cutting-edge advancements in medicine and biotechnology. We are keen to engage with candidates who can bring fresh perspectives and a high degree of creativity to our team. If you are a self-starter with an aptitude for simplifying complex scientific information, and an interest in medical writing for a variety of therapeutic areas, we encourage you to send us your resume and a portfolio of recent writing samples. Please highlight experience with the creation of content like that of peer-reviewed publications or educational assets for medical professionals. **Apply now!**Jersey City, NJRemote/HybridPart-time/Freelance$45-$65 per hourMedical Writing16 days ago
- We're a pioneering force in digital health, dedicated to enhancing patient care through innovative medical communication. As a Medical Writer in Chesapeake, VA, operating on a hybrid work model, your primary contribution involves developing high-quality, evidence-based medical content. Our expanding portfolio necessitates a diligent writer adept at translating complex medical jargon into accessible narratives. You’ll collaborate with a multidisciplinary team of clinicians, researchers, and regulatory specialists to produce compelling documents. Your mission encompasses crafting regulatory submissions, manuscripts, abstracts, and educational material, all whilst upholding rigorous scientific accuracy. **Primary Duties** * Compose meticulously researched scientific and clinical documents. * Guarantee precision and clarity in all forms of medical communication. * Partner closely with clinical teams, furnishing writing assistance from initial outline to final drafts. * Oversee projects from start to completion, satisfying time constraints and regulatory mandates. * Undertake literature reviews and data analysis to corroborate writing content. * Keep up to date with evolving industry guidelines and standards. **Essential Credentials** * Advanced academic background in life sciences, pharmacology, or a related field. A doctorate is preferred. * Demonstrable professional journey in medical writing or a comparable domain. * Exceptional command of scientific principles and medical terminology. * Mastery of regulatory guidelines for document submissions, including but not limited to FDA, EMA, and other governing bodies. * Proficiency in medical research, data analysis, and literature review. * Superb communication proficiencies, both in written and verbal forms. **The Perks of Joining Our Team** Beyond a stimulating scholarly environment and competitive financial rewards, we provide extensive learning opportunities, flexible work schedules, and an inclusive community ethos. Your professional evolution is supported via participation in seminars, courses, and conferences. Furthermore, our hybrid working paradigm offers a harmonious integration of office collaboration and remote productivity. We have a robust suite of healthcare offerings and wellbeing benefits. **Organizational Tenets** Our team thrives on principles of collegiality, ethical behavior, and continual learning. Our commitment to inclusivity encourages diversified perspectives, reinforcing originality and inventiveness. As a member, you'll significantly impact patient outcomes, driving advancements in healthcare technology and access. Embrace our calling, and become a cornerstone in reshaping the trajectory of medical awareness.Chesapeake, VAHybrid / RemoteFull-time$70,000 - $90,000 yearlyMedical Writingabout 1 month ago
- Our forward-thinking healthcare company based in Mesa, AZ, is actively seeking a talented and passionate Medical Writer to join our expanding clinical documentation team. The ideal candidate will possess a strong background in life sciences and a proven ability to translate complex medical information into clear, concise, and engaging content for various audiences. If you are a meticulous and detail-oriented individual with a passion for medical communication, we encourage you to apply! **Responsibilities in Detail** * Develop a wide array of medical documents, including clinical study reports, investigator brochures, protocols, and regulatory submissions, adhering to established guidelines and timelines. * Collaborate effectively with cross-functional teams, including clinicians, researchers, and regulatory affairs specialists, to gather and interpret relevant data and insights. * Conduct thorough literature searches and data analysis to support the creation of accurate and evidence-based medical content. * Ensure all documents comply with relevant regulatory requirements (e.g., FDA, EMA) and industry standards (e.g., ICH guidelines). * Proofread and edit medical documents for clarity, accuracy, grammar, and consistency. * Maintain awareness of current medical trends and advancements in the pharmaceutical and biotechnology industries. * Manage multiple projects simultaneously, adhering to strict deadlines and prioritizing tasks effectively. **Desired Expertise** * A solid academic background in a life science field (e.g., biology, chemistry, pharmacy) is strongly desired. * Prior exposure to medical writing or related pharmaceutical experience. * Proven proficiency in medical terminology, statistical concepts, and clinical research methodologies. * Exceptional writing, editing, and proofreading skills with keen attention to detail. * Demonstrated ability to interpret and analyze complex scientific data. * Excellent communication and interpersonal abilities, fostering collaboration with internal and external stakeholders. * A working knowledge of regulatory guidelines and industry standards related to medical writing. * Ability to effectively prioritize tasks and meet deadlines in a fast-paced environment. **What We Offer** Our company culture values a positive and supportive environment where employees feel empowered and engaged. We foster collaboration and innovation, encouraging our team members to excel and contribute their best. We promote continuous learning, supporting professional development opportunities for all employees. * Competitive salary and comprehensive benefits package, including health, dental, and vision coverage. * Generous paid time off (PTO) and holidays to encourage work-life balance. * Opportunities for professional development and advancement within the company. * A collaborative and supportive work environment where your contributions are valued. * Access to cutting-edge technology and resources to support your work. Our Mesa office offers a vibrant and engaging work environment, centrally located with access to local amenities and attractions. Be part of a company dedicated to improving healthcare through quality medical communications!Mesa, AZOn-site / HybridFull-time$80,000 - $110,000 yearlyMedical Writingabout 1 month ago
- Our rapidly expanding pharmaceutical client in Boston needs a meticulous and articulate part-time Medical Writer to contribute to our regulatory documentation efforts. As a vital member of our clinical team, your words will be instrumental in conveying essential information to regulatory bodies, healthcare professionals, and patients. **Your Impactful Contributions** * Drafting, reviewing, and editing clinical study reports, ensuring clarity, accuracy, and compliance with regulatory guidelines (e.g., FDA, EMA). * Creating compelling and evidence-based product monographs, white papers, and other promotional materials. * Collaborating with cross-functional teams including clinical research, data management, and medical affairs. * Conducting literature reviews and synthesizing scientific data to support medical writing projects. * Maintaining awareness of current medical and pharmaceutical industry trends and regulations. * Formatting documents according to specified style guides and submission requirements. **Core Attributes We Seek** * Advanced degree (Master’s or PhD) in a scientific discipline, such as biology, pharmacology, or related field. * A background in medical writing, particularly with clinical study reports or regulatory documents. * A portfolio that features your ability to synthesize intricate scientific data into clear and engaging writing. * Fluency in medical terminology, statistical concepts, and clinical research principles. * Exemplary writing, editing, and proofreading abilities, paying strict attention to detail. * Superb organizational and time-management skills to handle multiple projects simultaneously. * Capacity to thrive in both remote and in-office environments. * Strong communication skills to present technical information clearly. **Professional Development & Company Culture** We support professional development with comprehensive training opportunities. Benefits encompass health coverage, a retirement plan, paid time off, and opportunities for hybrid/remote flexibility. Boston is a global hub for medical innovation, offering access to industry events and a concentration of leading pharmaceutical companies. We are serious about developing our talent to promote from within and grow with the organization. *Embrace a collaborative and respectful workplace where individual contributions are highly regarded. *Benefit from a culture where innovation and evidence-based decision-making is highly regarded. *Work in an environment where quality and ethics are our core values. **Beyond Compensation** Your health and well-being are also priorities for us, and your total reward is composed of wellness programs and resources that go far beyond compensation and traditional benefits offerings. *Medical, dental, and vision coverage *Paid life and disability insurance *Employee assistance program *Financial, legal and identity theft resources *Generous PTO *Paid holidays *Paid leave If you have a passion for translating complex medical data into clear, impactful communications, and seek a rewarding part-time opportunity within a dynamic team, apply now! Make your mark in the Boston medical community.Boston, MAHybrid/RemotePart-time$40,000 - $65,000 per yearMedical Writingabout 1 month ago
- 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 Writingabout 2 months ago