Oversee adaptation, submission, and governance of digital content for DTC healthcare and pharmaceutical web properties.
Act as a strategic liaison between Brand Teams, Product Owners, Agency Partners, and Regulatory Reviewers.
Maintain pristine consumer copy standards and drive post-review content updates while ensuring regulatory safety.
New Era Technology securely connects people, places, and information with end-to-end technology solutions at scale. With a global team of over 3,000 professionals, they are committed to creating a workplace where everyone feels valued, empowered, and inspired to grow.
Edit and review informed consent forms to ensure regulatory compliance and clarity.
Collaborate with IRB members, sponsors, and sites to incorporate required language.
Mentor junior editors and contribute to process improvements for quality control.
The partner company provides specialized services for clinical research and regulatory compliance. It fosters a collaborative environment and emphasizes ethical research practices, though team size is not specified.
Lead development of complex medical writing and publication deliverables for clinical studies.
Define document strategies and coordinate writing activities across multidisciplinary teams.
Mentor less experienced writers and enhance processes to ensure high-quality outputs.
A global life sciences and healthcare company offering integrated services across the industry. It fosters an inclusive, collaborative culture focused on employee growth, professional development, and delivery of important therapies.
Conduct structured quality reviews of proposals to ensure compliance, consistency, and responsiveness.
Edit and evaluate proposal content against style guides, bid guidelines, and brand voice.
Partner with proposal writers and subject matter experts to provide constructive edits and feedback.
This partner company helps healthcare organizations improve proposal quality and competitiveness. It offers a collaborative, fast-paced environment with a focus on professional development and quality improvement.
Lead development of high-quality, strategic copy across multiple platforms for healthcare and pharmaceutical marketing.
Write and refine persuasive, compliant content translating complex scientific data into compelling narratives for HCP and patient audiences.
Mentor junior copywriters, providing feedback and training to strengthen their writing and strategic thinking.
Inizio Evoke is a global health marketing, communications, and transformation platform that uses data-driven insights and human centricity to create creative solutions for health decisions. They are a large company committed to diversity and inclusion, offering a remote work environment with company-paid benefits.
Lead author on complex regulatory and clinical documents including protocols, CSRs, IBs, and IND/NDA/BLA submissions.
Provide strategic input on document planning, messaging, and quality control while mentoring other writers.
Manage multiple projects independently, balancing timelines and client expectations in a fully remote environment.
Eldridge Writing provides top-tier medical writing services to pharmaceutical and biotechnology clients. We are a small, collaborative team that values quality and serves as a true extension of our clients’ teams.
Develop high-quality, medically accurate promotional content for pharmaceutical clients.
Conduct literature reviews and manage multiple projects with strict deadlines.
Collaborate with multidisciplinary teams and mentor junior staff.
The company is a medical communications agency that supports pharmaceutical and life sciences clients with promotional and medical content. It fosters an inclusive and collaborative workplace committed to equal employment opportunity and professional growth.
Develop and write medically accurate content for a variety of resources, including value proposition slide decks, advisory boards, and internal training materials.
Serve as content point person on assigned accounts, ensuring high-quality work under limited supervision and strict timelines.
Collaborate with internal teams and pharmaceutical clients, attend medical/legal/regulatory review meetings, and mentor junior staff.
PRECISION AQ is a top payer marketing agency that supports global pharmaceutical and life sciences clients in commercial excellence. The company focuses on demonstrating the economic, clinical, and societal value of medical treatments to payers, providers, patients, and policymakers.
Research and develop technical materials ensuring accuracy and editorial style.
Partner with clients and KOLs on content development and attend scientific meetings.
Create materials for different medical audiences in various media formats.
ApotheCom is a leader in medical communications, providing high-quality medical communications programmes. As part of Inizio, a global healthcare consulting group with over 10,000 employees, they foster a diverse and inclusive workplace.
Critically evaluate scientific literature and produce accurate regulatory documents.
Manage writing assignments across multiple projects and ensure timely delivery.
Work directly with clients and multidisciplinary teams on regulatory submissions.
A partner company in the pharmaceutical, biotechnology, and medical device sectors is hiring a Senior Medical Writer. The company offers a fully remote environment and opportunities to work on a broad portfolio of clinical and regulatory documents.
Responsible for generating creative ideas and shaping work across multiple projects.
Requires strong copywriting and strategic thinking in a healthcare agency setting.
Collaborates with art directors and presents work to clients with confidence.
P10 is a remote-only agency that redefines creative services by challenging traditional processes and prioritizing change and efficiency. The company brings together a diverse team of seasoned professionals driven by passion and purpose, delivering exceptional value to clients.
Oversee content compliance review for marketing, educational, and communications materials, ensuring alignment with pharmacy regulations and FDA/FTC guidelines.
Collaborate cross-functionally with Compliance, Clinical, Marketing, and Legal teams to provide risk-based guidance and streamline content approval workflows.
Develop training resources, manage review queues in Asana, and maintain auditable documentation to support compliance and process improvement.
Strive Pharmacy is a personalized compounding pharmacy focused on individualized care, creating medications tailored to each patient's needs. The company is growing and fosters a culture of community and professional development, with team events and a commitment to employee growth.
Provide medical writing services and consultation to clinical research scientists and academic partners, including researching, writing, and editing scientific information.
Lead content planning and production of regulatory documents such as protocols, investigator brochures, and clinical study reports.
Act as primary contact and liaison with external publication executives and editors to coordinate content and revisions.
Alimentiv is a medical research organization providing medical writing services and consultation to clinical research scientists and academic partners. The company culture emphasizes continuous improvement and teamwork.
Develop and manage medical content for pharmaceutical, biopharma, and device clients, including SRDs, FAQs, and slide sets.
Drive document development from material gathering through MLR review, using tools like Veeva PromoMats.
Collaborate with global teams to ensure timely, high-quality, compliant deliverables that meet client needs.
EVERSANA provides next-generation commercialization services to the life sciences industry. With over 7,000 employees globally, the company serves more than 650 clients and is certified as a Great Place to Work, fostering an inclusive culture.