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.
Independently plans and prepares regulatory documents and medical communications for all phases of product development.
Organizes, analyzes, interprets, and presents scientific and statistical information per ICH guidelines.
Collaborates with cross-functional internal and external document production teams.
Veristat is a global contract research organization with over 30 years of expertise accelerating life-changing therapies to patients worldwide. The company has a flexible, inclusive culture with a 70% remote workforce and 66% women-led teams.
Independently plans and prepares regulatory documents and medical communications to support all phases of product development.
Organizes, analyzes, interprets, and presents scientific and statistical information in accordance with industry guidelines (ICH, ICMJE, GPP).
Collaborates with cross-functional internal and external teams under direction of Medical Writing management.
Veristat is a global contract research organization that accelerates life-changing therapies to patients worldwide. With over 30 years of expertise, the company has supported more than 105 approved therapies and fosters a flexible, inclusive culture with 70% remote workforce and 66% women-led teams.
Lead the preparation of complex clinical and regulatory documents including Clinical Study Protocols, Clinical Study Reports, and Investigator Brochures.
Collaborate with clinical development teams and stakeholders to produce accurate, compliant, and scientifically robust documentation.
Manage document timelines, review cycles, and project deliverables while ensuring quality standards and regulatory requirements are met.
Our partner is a specialized medical writing team supporting the development of high-quality regulatory documentation for the global pharmaceutical industry. It offers a collaborative, remote environment focused on quality, precision, and scientific communication.
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 high-quality, evidence-based medical content for healthcare professionals that supports clinical integrity and commercial objectives.
Translate complex scientific information into clear, compelling communications across print and digital formats.
Collaborate with cross-functional teams including medical, legal, and design to manage multiple projects and meet timelines.
Montu is Australia's largest healthtech business focusing on alternative healthcare, supporting patients, doctors, and pharmacies. Founded in 2019, Montu has been recognized as Australia's fastest-growing tech company with a driven and results-focused culture.
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.
Build and maintain scientific relationships with healthcare professionals and medical experts.
Gather and communicate medical insights to inform research and strategy.
Collaborate with cross-functional teams to support evidence-based discussions and healthcare initiatives.
The company is a healthcare organization focused on advancing innovative therapies and improving patient outcomes. While the specific size is not disclosed, the culture is collaborative, inclusive, and supportive of professional growth.
Develop and manage medical content for client engagements, including Scientific Response Documents and FAQs.
Drive document development from material gathering to facilitating medical, legal, and regulatory review meetings.
Collaborate with global teams and participate in key client meetings to ensure high-quality deliverables.
EVERSANA provides next-generation commercialization services to the life sciences industry, helping bring innovative therapies to market. With a global team of more than 7,000 employees, they are committed to creating a healthier world and embrace diversity and inclusion.
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.
Provide technical writing support for safety, epidemiology, registry, and risk management program operations.
Develop, revise, and finalize program reports, including Knowledge, Attitudes, and Behavior (KAB) survey outcome reports.
Collaborate directly with program operations teams to understand requirements and deliver high-quality documentation.
Jobgether uses AI-powered matching to connect candidates with hiring companies for job applications. They operate as a partner company managing applications and next steps for various positions.
Provide strategic medical communication recommendations to support brand goals.
Lead execution of content development activities for oncology accounts.
Manage writing tasks including research, data-checking, and reference annotation.
Lockwood partners with pharmaceutical, biotech, and medical device companies to develop science-based medical communications strategies. Over a third of our staff hold advanced scientific or medical degrees, and our flexible remote structure supports work-life balance and attracts top talent.
Develop and execute publication strategies aligned with client objectives and evidence priorities across manuscripts, abstracts, posters, and congress activity.
Provide senior scientific oversight to ensure accuracy, clarity, and strategic alignment across deliverables including scientific platforms, core decks, and advisory board materials.
Serve as a senior scientific and strategic client contact, building trusted relationships and guiding content priorities and data interpretation.
Real Chemistry is a global healthcare communications and marketing agency that uses deep scientific expertise, human-centered creativity, and AI-driven insights to transform healthcare. The company is Great Place to Work certified and fosters a culture of collaboration and excellence.