Edit and ensure regulatory compliance for pharmaceutical marketing materials across digital and print channels.
Fact-check and proofread copy to adapt for new channels and audiences, providing medical expertise within FDA guidelines.
Collaborate with cross-functional teams and manage multiple projects in a fast-paced environment.
P10 is a creative agency focused on delivering exceptional value for clients. It is a remote-only team of diverse, seasoned professionals driven by passion and purpose.
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.
Prepare and maintain Trial Master Files for clinical studies, ensuring completeness and compliance.
Review documentation for accuracy and alignment with protocols and regulations.
Communicate with sponsors, project managers, and sites to resolve documentation issues.
Jobgether is an AI-powered job matching platform that connects candidates with hiring companies. They foster an inclusive, collaborative, and respectful workplace, utilizing technology to ensure fair recruitment.
Coordinate day-to-day execution of clinical studies including site onboarding, documentation, and timeline tracking.
Support regulatory compliance through IRB submissions, amendments, and maintaining study documentation.
Collaborate cross-functionally with science, bioinformatics, and product teams to ensure study operations.
Tiny Health advances lifelong health through precision microbiome science using shotgun metagenomics and AI. Founded in 2020, it is a remote-first startup with a diverse international team focused on making the microbiome measurable and actionable.
Process medical records requests accurately and within required timeframes.
Ensure HIPAA compliance and validate patient authorizations.
Perform quality-control reviews and maintain secure handling of protected health information.
The company specializes in securely processing medical records requests for healthcare clients. It maintains a collaborative and compliance-focused culture with a strong emphasis on accuracy and privacy.
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.
Support Communications Consultants by coordinating accurate and compliant participant communications.
Draft, edit, and proof participant-facing materials using standardized templates.
Track deliverables and project milestones using project management tools.
Voya Financial is a leading retirement, employee benefits and investment management company. The company supports over 18 million customer relationships and has been certified as a Great Place to Work for 10 consecutive years.
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.
Write, edit, and coordinate clear, accurate health communications for diverse audiences.
Collaborate with communications, policy, scientific, and media teams to develop educational materials.
Manage content creation, outreach strategies, and communications metrics to support public health initiatives.
This role supports federal public health communications, writing and editing content for scientific and policy-focused initiatives. The partner company is an equal opportunity employer that collaborates with communications, scientific, and technical professionals on mission-driven projects.
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.
Lead portions of regulatory assessments, external audits, and accreditation processes for Commercial, Medicare, Medicaid, and Marketplace departments.
Act as primary point of contact for internal and external partners on regulatory activity, quality efforts, SOP development, and client delegation agreements.
Maintain regulatory gap status reporting, track work streams, and lead change management related to regulatory requirements.
Prime Therapeutics is a pharmacy benefit manager (PBM) with a purpose beyond profits, reimagining pharmacy solutions to connect care for those they serve. The company is a large, purpose-driven organization focused on simplifying healthcare and fostering a collaborative culture.
Provide regulatory guidance throughout the clinical development lifecycle and prepare quality regulatory submissions.
Compile, coordinate, and review applications to regulatory authorities, including CTA/IND and amendments.
Represent Global Regulatory Affairs at project team and business development meetings, overseeing Regulatory Affairs Specialists.
Precision Medicine Group is a life sciences company providing clinical research, regulatory, and commercial services to biopharmaceutical clients. It fosters a collaborative, quality-focused culture and is an Equal Opportunity Employer.
Review consent language, disclosure protocols, and microdata releases to ensure compliance with federal laws and agency requirements.
Advise program staff on regulatory and procedural compliance matters tied to research ethics and data protection.
Provide statistical disclosure review of microdata files and tables prior to public release.
FWI supports the Centers for Disease Control and Prevention (CDC) by safeguarding the confidentiality and regulatory integrity of national health data. The company is rapidly expanding and recognized as a 2024 and 2025 Top Workplace by the Washington Post, offering growth opportunities in a collaborative environment.
Engage with patients to recruit, educate, and pre-screen them for clinical studies.
Maintain data accuracy across multiple study portals and manage data entry and queries.
Collaborate with site teams and PIs to ensure protocol compliance and resolve issues.
Care Access brings world-class research and health services directly to communities, working to make the future of health better for all. With hundreds of research locations and a global team, we are dedicated to ensuring every person can contribute to medical breakthroughs.
Independently manages significant aspects of clinical trials and research projects.
Trains and provides guidance to less experienced staff, and oversees data management.
Ensures compliance with regulations, monitors IRB submissions, and interfaces with study sponsors.
Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate and prepare leaders for the future. The university is committed to diversity and inclusion, providing a supportive environment for staff and faculty.
Manage the intake, review, analysis, and reporting of Individual Case Safety Reports (ICSRs) and support Clinical Events Committees and Data Monitoring Committees.
Co-author and maintain study-specific safety documents and prepare aggregate safety reports for regulatory submission.
Collaborate with sponsors, study teams, and cross-functional partners to ensure data quality and compliance with GCP and GVP standards.
This partner company delivers high-quality safety services across clinical research and medical device programs. They foster a collaborative, detail-oriented environment with a focus on compliance and patient outcomes.