Support senior leadership in strengthening the strategic presence of medical writing across therapy areas.
Drive resource planning, performance tracking, and process simplification to improve efficiency.
Lead transformation initiatives and contribute to long-range planning and annual operating activities.
This partner company operates a global regulatory medical writing function, supporting strategic evolution and operational excellence across therapy areas. It emphasizes collaboration among senior leadership, internal teams, contractors, and vendors within a remote work environment.
Develop and execute content strategy and production for healthcare member communications across email and digital hubs.
Own content libraries, produce case studies, and direct freelance and AI-assisted content capacity.
Collaborate with cross-functional teams to ensure brand consistency, compliance, and measurable engagement.
They are a healthcare services company specializing in member-facing communications and content across multiple service lines. The company is virtual-first and values flexibility, innovation, and AI-enabled production methods.
Develop scientific expertise in assigned therapeutic areas and support delivery for a versatile team.
Research and develop technical materials, ensuring accuracy in content, editorial style, and references.
Communicate with clients and key opinion leaders on content development and attend scientific meetings.
iNIZIO Medical is a medical communications company creating compelling content and engaging communities across the healthcare spectrum. With over 2,000 employees globally, we foster a culture of diversity, inclusion, and belonging.
Support Clinical Trial Managers with study start-up, protocol development, and Trial Master File preparation.
Coordinate with clinical sites on documentation, training, and compliance with FDA and GCP requirements.
Assist with tracking study payments and providing operational support across the full study lifecycle.
The company is a partner organization specializing in clinical research and development, operating through Jobgether. It offers a structured clinical operations environment with cross-functional teams and professional growth opportunities.
Oversee the development of technically accurate, high-quality deliverables for Publications/Medical Affairs accounts.
Serve as a strategic partner to clients, ensuring projects and deliverables are on time and within budget.
Direct the editorial component of projects and lead a team of medical writers, ensuring accuracy and quality of all written material.
Lumanity is dedicated to improving patient health by accelerating and optimizing access to medical advances, partnering with life sciences companies to generate evidence and translate science into compelling product narratives. The company operates globally across areas such as Asset Optimization and Commercialization, Value Access and Outcomes, and Medical Strategy and Communications, fostering a collaborative culture focused on medical and commercial success.
Manage designated Medicaid, EQR, compliance, and quality improvement projects through all stages from planning to completion.
Coordinate with internal teams, external partners, and stakeholders to ensure project milestones and deliverables are met.
Prepare reports, workplans, and presentations while monitoring project progress and identifying risks.
Health Services Advisory Group (HSAG) is a healthcare organization dedicated to improving the quality of healthcare delivery. The company is a growing team that transforms healthcare in the United States, fostering a culture of community and fun.
Lead medical information activities for healthcare programs, ensuring high-quality handling of inquiries.
Ensure accurate documentation and triage of medical requests, adverse events, and product complaints.
Manage multiple projects and maintain empathetic customer communication across channels.
The hiring company focuses on delivering medical information and healthcare support programs. It operates with a remote team culture, emphasizing collaboration and professional development.
Develop and maintain integrated project plans for global regulatory submissions, ensuring adherence to scope, timelines, budgets, and quality standards.
Act as the primary regulatory timeline contact across Clinical, Nonclinical, CMC, Quality, and Commercial functions, fostering collaboration and alignment.
Identify and mitigate project risks, prepare teams for agency meetings, and lead responses to regulatory queries from global health authorities.
Centessa Pharmaceuticals is a clinical-stage company developing orexin receptor 2 agonists for narcolepsy and other sleep-wake disorders. As a wholly owned subsidiary of Eli Lilly and Company, it shares a culture of caring and impact with over 50,000 employees.
Drive forward movement within the post-trial pipeline by proactively removing barriers and ensuring timely progression.
Obtain medical records and prescriptions from prescribers while maintaining accurate client records in CRM.
Communicate consistently with speech language pathologists, clients, and care providers to complete sales and secure funding.
Lingraphica is a mission-driven organization providing speech-generating devices to help people with communication impairments improve their quality of life. They are a leader in augmentative and alternative communication technology, with a fast-paced, goal-oriented culture focused on helping individuals, families, and care teams.
Lead medical and scientific review of promotional and non-promotional materials for assigned products and markets.
Ensure scientific accuracy, regulatory compliance, and fair balance in content, collaborating with cross-functional teams.
Develop and review medical content, including scientific narratives and medical information, adhering to industry standards.
EVERSANA provides next-generation commercialization services to the life sciences industry, helping bring innovative therapies to market. With over 7,000 employees globally, they serve more than 670 clients and are certified as a Great Place to Work.
Lead strategic medical communication recommendations and scientific content development for assigned accounts.
Oversee creation of manuscripts, posters, abstracts, and other publication deliverables across therapeutic areas.
Supervise Associate Scientific Directors and collaborate with in-house or freelance staff on research, writing, and data-checking tasks.
Lockwood collaborates with clients in the pharmaceutical, biotech, and medical device industries to identify effective, holistic, science-based strategies through medical communications. Over a third of our staff hold advanced scientific or medical degrees, and most work from where they live, fostering a flexible, talent-focused culture.
Drive product strategy and market analysis to identify healthcare opportunities.
Collaborate with engineering, sales, marketing, and leadership to deliver products.
Champion healthcare data interoperability and evangelize product roadmaps.
Smile Digital Health is a healthcare technology company providing a FHIR-based data liberation platform that enables healthcare stakeholders to collect and exchange data. The company operates in over 20 countries, ranked #19 on Deloitte's Technology Fast 50 in 2024, and fosters a culture of respect, inclusion, and belonging.
Provide real-time EHR charting support to physicians during outpatient visits.
Accurately document patient encounters and interpret clinical terminology.
Maintain HIPAA-compliant workflows and complete medical records efficiently.
This company provides virtual medical scribe services, supporting physicians with real-time EHR documentation during patient encounters. It offers a fully remote work environment with a collaborative culture focused on healthcare technology and professional development.