Scientific Affairs Writer

POSITION SUMMARY: The Medical Writer plays a key role in drafting abstracts, posters, manuscripts for peer-review, and other documents as part of the scientific communications team. PRIMARY RESPONSIBILITIES: Draft and copyedit submissions for abstract, posters and peer-reviewed manuscripts. Support writing activities as needed for internal validation documents, clinical trial protocols and regulatory submissions or reimbursement dossiers. Work collaboratively with other team members and actively participate in pub planning activities and managing various writing projects Work collaboratively and manage project timelines when working with extended teams (Clinical Research, Medical Affairs, RD, Marketing, and others) Format manuscript and abstracts following journal/congress guidelines Create and maintain project records on internal publications tracker Perform fact/data check on writing documents (manuscripts, white papers, dossiers, etc.) Adhere to SciComm’s writing style guide while copyediting and formatting scientific documents Manage a list of upcoming congresses with meeting and abstract submission due dates for various congresses Follow GPP3 and ICJME guidelines in compliance with good publication practices. Track manuscript/abstract status online, once submitted Keep accurate records of publications content and archive materials relating to completed publications QUALIFICATIONS: Doctoral degree (PhD or PharmD) in Biology, Molecular Genetics, Molecular Biology, oncology, genetics and genomics or other relevant scientific discipline, Medical Degree (MD), or equivalent required. Two or more years scientific writing experience, focusing on peer-reviewed publications or grants as part of university or any industry (biotechnology, pharmaceutical, medical device, or medical communications) or have an extensive academic publication record. Experience submitting abstracts and manuscripts to congresses and journals. Experience developing posters for congresses Good understanding of ICMJE and GPP guidelines KNOWLEDGE, SKILLS, AND ABILITIES: Ability to work in a fast-paced environment. Strong interpersonal and communication skills Excellent organizational skills, especially the ability to prioritize, meet deadlines and multi-task. Ability to work cross­ functionally, collaborate, and be a team player. Excellent attention to detail An ability to maintain a positive and professional attitude Familiarity with electronic literature search tools and obtaining copyright permissions. Strong Microsoft Office (Word, Excel, PowerPoint) skills; experience using Adobe Creative Suite/Creative Cloud (Illustrator, Professional, and InDesign), Graphpad and Endnote is a plus. PHYSICAL DEMANDS WORK ENVIRONMENT: Duties are typically performed in an office setting and environment. This position requires the ability to use a computer keyboard, communicate over the telephone and read printed material. Duties may require working outside normal working hours (evenings and weekends) at times. The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations. Remote USA $80,000 $100,000 USD OUR OPPORTUNITY Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives. The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Nater ... (truncated, view full listing at source)