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.
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.
Develop scientific expertise in assigned therapeutic areas, supporting delivery for a versatile team.
Research and develop technical materials, ensuring accuracy and adherence to editorial style.
Communicate with clients and key opinion leaders on content development and attend scientific meetings.
Nucleus Global is a global leader in medical communications, part of the iNIZIO group, providing advisory, medical, marketing, and engagement services to life sciences companies. With over 900 employees across Europe, US, and APAC, it fosters a friendly and informal working environment with social events and wellbeing programs.
Develop high-quality clinical and regulatory documents supporting global submissions
Partner with cross-functional teams to transform complex scientific data into clear narratives
Ensure compliance with regulatory requirements while managing document timelines
Acadia Pharmaceuticals is a biopharmaceutical company developing innovative therapies to address unmet medical needs in neuroscience. With a collaborative and patient-focused culture, the company is committed to advancing treatments that improve lives.
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.
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.
Prepares clinical and regulatory documents for drug and device development with moderate autonomy.
Coordinates review, approval, and quality control of clinical and regulatory projects.
Develops understanding of submission strategies, regulations, and project management to drive objectives.
AbbVie discovers and delivers innovative medicines and solutions for serious health issues across immunology, oncology, neuroscience, and aesthetics. The company is a global biopharmaceutical leader with a strong focus on research and development, employing thousands worldwide.
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.
Write and develop scientific publications including manuscripts, abstracts, and posters for oncology products.
Review and ensure highest standards of content produced by junior team members.
Provide line management and mentorship to support team development.
Inizio is a strategic partner for health and life sciences, solving health challenges and developing transformational ideas. We are a team of 10,000 experts in 35 countries, fostering an inclusive and empowering culture.
Craft and review regulatory documents such as clinical study reports, protocols, and investigator's brochures.
Collaborate with a supportive team to exceed client expectations.
Learn the intricacies of drug development and the science behind pharmaceuticals and biologics.
Eldridge Writing is a growing firm providing top-tier medical writing services to pharmaceutical and biotechnology clients. They pride themselves on quality and mentorship of the next generation of medical writers.
Develop and deliver multiple oncology publications including manuscripts, abstracts, posters, presentations, and congress materials.
Interpret and communicate complex clinical and scientific data accurately with authors and subject-matter experts.
Manage multiple projects and deadlines across a busy account while applying publication guidelines and ethical standards.
ApotheCom is a global medical communications agency that partners with pharmaceutical and biotech companies to translate complex science into compelling communications. They have a collaborative, inclusive culture and value scientific expertise.
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.
Lead scientific strategy and content development for oncology medical communications programs.
Partner with senior scientific leaders and clients to translate complex clinical data into accurate, compelling communications.
Manage multiple projects, mentor junior team members, and ensure compliance with professional standards.
Our partner is a medical communications company that develops promotional medical education materials for oncology. They offer a flexible, collaborative remote work environment with a focus on scientific accuracy and evidence-based communication.
Lead the PV Medical Writing function, ensuring high-quality, compliant, and timely deliverables.
Manage and develop the PV Medical Writing team, fostering performance, engagement, and professional growth.
Drive quality, compliance, inspection readiness, and continuous improvement initiatives, including oversight of SOPs, KPIs, audits, and regulatory inspections.
PrimeVigilance is a global pharmacovigilance specialist helping clients navigate complex regulations while keeping patient safety at the center of every decision. With teams across Europe, North America, South America, Asia and Australia, we foster a culture of kindness, flexibility, growth, and belonging.
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.
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.
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.
Lead scientific strategy and content development for oncology-focused medical communications programs.
Serve as a senior scientific partner to clients, driving brand planning and new business initiatives.
Manage multiple projects with rigorous editorial standards and cross-functional collaboration.
This role is listed on behalf of a partner company that provides AI-powered job matching services. Jobgether is a platform that uses AI to connect candidates with hiring companies, emphasizing efficiency and objectivity in recruitment.
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.