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 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 scientific materials such as slide decks, infographics, and social media posts to support medical affairs strategy.
Translate clinical and health economic evidence into clear, compliant content for internal and external stakeholders.
Coordinate with cross-functional teams and external vendors to deliver high-quality materials on time.
Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines for hypertension and related comorbidities like chronic kidney disease and sleep apnea. It is headquartered in Radnor, Pennsylvania, operates as a fully remote company, and fosters a diverse and dynamic team culture.
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.
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.
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 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.
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 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.
Lead the development of disease-state and product-specific materials and the omni-channel scientific communications strategy.
Oversee the development of standard and custom responses to unsolicited requests and create internal Medical Information resources.
Lead publication strategy and execution for clinical and nonclinical data including manuscripts, abstracts, posters, and presentations.
Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities. The company is fully remote and headquartered in Radnor, Pennsylvania.
Provide scientific and medical direction to integrate clinical relevance into client brand strategies.
Monitor disease categories and product labeling to derive actionable insights for medical strategy.
Support senior Medical staff in new business and thought leadership while training junior team members.
Inizio Evoke is a healthcare communications agency that aims to make health more human through strategic and creative work. They foster an inclusive, authentic culture and offer flexible work environments with a focus on collaboration and professional growth.
Develop high-quality, medically accurate scientific content for brand goals.
Engage with KOLs and HCPs while managing resources and timelines.
Conduct background research, data-checking, and reference annotation.
Lockwood collaborates with pharmaceutical, biotech, and medical device clients to create holistic, science-based medical communication strategies. Over a third of staff hold advanced degrees, and most work remotely, fostering a flexible structure and work-life balance.
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.
Provide medical information responses to healthcare professionals and patients, including triaging drug information inquiries and disseminating responses verbally or in writing.
Identify and intake adverse events and product quality complaints, ensuring compliance with client SOPs and regulatory requirements.
Utilize drug information skills to critically evaluate medical literature and develop written correspondence for healthcare professionals.
EVERSANA provides next-generation commercialization services to the life sciences industry. With a global team of over 6,000 employees, we are committed to creating a healthier world and embracing diversity.
Plan, develop, and oversee scientific content for oncology accounts across multiple therapeutic areas.
Lead client interactions, brand strategy, and the scientific portion of brand planning and business development.
Manage resource allocation, develop SOWs, and identify areas for new and organic growth.
Lockwood collaborates with pharmaceutical, biotech, and medical device clients to develop science-based medical communication strategies. Over a third of its staff hold advanced scientific or medical degrees, and most work remotely, fostering a flexible, work-life balanced culture.
Lead projects from conception to completion, crafting outlines and manuscripts per strategic guidelines.
Present to clients and defend pieces at LMR meetings.
Manage multiple teams and workstreams efficiently, empowering junior creatives.
Avalere Health is a global healthcare advisory, medical, and marketing company united by the purpose of reaching every patient possible. It fosters an inclusive culture with employee network groups, flexible work, and professional development opportunities.
Lead global publications teams in thrombolytics and respiratory.
Partner with senior clients on high-impact publications and strategy.
Oversee and mentor junior writers in a supportive team environment.
We are a global leader in the medical communications space, with more than 900 people across Europe, the US and APAC. We pride ourselves on setting the standard for industry best practices, with unparalleled dedication to impactful and innovative communication.
Plan and execute marketing projects and programs, supporting regional and local marketing teams.
Act as super user for key BD tools (Veeva Vault, AdProm, ShowPad) to ensure efficient and compliant marketing processes.
Support development of marketing materials, website updates, and management of marketing events and congresses.
BD is a global medical technology company that develops and manufactures medical devices and solutions to advance health. With a large, multinational team, BD fosters a culture of collaboration, compliance, and quality.
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.