Flatiron Health is a healthcare technology and services company focused on accelerating cancer research and improving patient care. Our platform enables cancer researchers and care providers to learn from the experience of every patient. We believe that existing clinical research paradigms are ill-equipped to answer the research questions that face drug developers, academic researchers, and regulators in the oncology space today.
Flatiron Research is focused on innovating in the real-world evidence (RWE) and clinical trials space. Our technology-first approach has allowed us to build RWE data sets with higher quality, accuracy, recency, and scale than any other cancer data that are available. We have active partnerships with top-tier academic medical centers, the top 15 oncology biopharma companies, the FDA, and the NCI, all focused on using data to accelerate the research and treatment of cancer.
We're looking for an experienced clinical regulatory medical writer, interested in innovation and looking to be a key member of research teams in a fast-paced, mission-driven environment. Here's what you need to know about the role, our team and why Flatiron Health is the right next step in your career.
In this role, you will be a leading individual contributor for our medical writing function across the organization, working with cross-functional teams to ensure Flatiron delivers high quality documents to our life sciences partners and other strategic collaborators as needed. In addition, you will:
In this role, you will get the opportunity to work with a wide range of cross functional teams such as Regulatory Affairs, Regulatory Policy, Integrated Quality Management, Life Sciences Partnerships, Research Oncology, Product, Research Operations, and Quantitative Sciences.
You're a clinical and regulatory writing professional with 5 or more years of medical writing experience within the biopharma industry, with experience ideally across all aspects of documents including but not limited to protocols, SAPs, clinical study reports, regulatory briefing books, supplemental new drug/biologic license applications, and Ex-US regulatory submission expertise is beneficial but not required. You're excited by the prospect of rolling up your sleeves to tackle meaningful problems each and every day. You’re a kind, passionate and collaborative problem-solver who seeks and gives candid feedback, and values the chance to make an important impact.
Extra Credit:
A career at Flatiron is a chance to work with everyone involved in the future of cancer care and research—all under one roof. Research oncologists, data scientists, including epidemiologists and biostatisticians, designers, clinicians, software engineers and other subject matter experts contributing to our research projects, and many more all work together to improve cancer care and accelerate research.
You'll also find a culture of continuous learning, broad and inclusive employee support offerings, and a commitment to supporting our team members in all aspects of their lives—at home, at work and everywhere in between. We offer:
Flatiron Health is proud to be an Equal Employment Opportunity employer.
We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Flatiron Health was founded in 2012 and became an independent affiliate of the Roche Group after its acquisition by Roche in 2018. It prides itself as a healthtech company dedicated to helping cancer centres thrive and deliver better patient care.
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