Biomedical Writer
$84k - $89kCadent, powered by Syneos Health
Description Meticulous doesn't begin to describe your dedication to accuracy. You express all your ideas effortlessly and have the skills to distill other people's ideas into their best possible form. Your messaging is not only clear and concise, but your medical expertise allows you to convey high-level scientific knowledge in meaningful and comprehensible communications. You will support content development across multiple clients and disease areas. Responsibilities Develop scientific educational content including slide decks, messaging documents, and publications (posters, manuscripts). Conduct literature searches and other desktop research to build understanding of new therapeutic areas as needed. Collaborate with internal medical team to develop content for medical educational programs in the form of slides, text, and videos/scripts. Participate in client meetings to review content and collect feedback. Ensure content is scientifically accurate and supported by original references. Develop visual representation of complex data to facilitate audience understanding. Fact‑checking and quality control (ensuring content developed by other writers is supported by scientific evidence). Update content based on internal and client team feedback. Collaborate with account and medical counterparts to track project deadlines. Develop knowledge in multiple disease areas. Experience in oncology and/or hepatology is a plus but not required. Build understanding of the pharmaceutical industry and clinical development cycle. Ability to prioritize/organize workload and manage multiple workstreams. Build understanding of client dynamics and expectations. Participate in client‑facing meetings. Travel (e.g., advisory board, conferences) or on‑site client visits may be required around 10% of the time, as needed. Essential Requirements Education: PhD, MD, or PharmD. 0–1 years of pharma or medical communication agency experience. Excellent interpersonal skills with the ability to collaborate with various functional teams (accounts, editorial, creative). Analyze and synthesize complex information from multiple sources and communicate medical/technical information to a wide variety of audiences. Work in a fast‑paced, deadline‑driven, team‑oriented environment. Efficiently prioritize multiple tasks and communicate effectively with others; can quickly evaluate the resources and potential challenges and communicate with the team in an actionable manner. Desired Requirements EndNote reference management database experience. Prism GraphPad experience. Compensation and Benefits The annual base salary for this position ranges from $84,000 to $89,000. Depending on qualifications, skills, and performance, additional compensation may include commissions or bonuses. Benefits for this position include a competitive compensation package and health benefits (medical, dental, and vision), company match 401(k), flexible paid time off (PTO) and sick time. Eligibility for paid sick time may vary depending on where you work. EEO Statement Syneos Health companies are affirmative action/equal opportunity employers (Minorities/Females/Veterans/Disabled). #J-18808-Ljbffr Cadent, powered by Syneos Health
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...in medical device engineering, particularly for cardiovascular technologies. Candidates should have a Bachelor’s in Mechanical or Biomedical Engineering and at least 8 years of related experience. The role involves overseeing engineering projects and ensuring compliance...BiomedicalFull time- ...leading pharmaceutical company is hiring a Sr. Regulatory Specialist for a fully remote position. This role requires a Ph.D. in Biomedical Science and expertise in regulatory affairs, particularly in IVD product development. The specialist will collaborate with R&D teams...BiomedicalRemote jobFlexible hours
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$70.1k - $145k
...Job Responsibilities Senior medical writer on clinical study or regulatory project teams. Writes, edits, and coordinates content for clinical/regulatory documents while serving as the primary technical contact with the internal team and the client. Core Responsibilities...Flexible hours$70 - $80 per hour
A consulting firm specializing in IT is looking for a Senior Medical Writer to manage the medical writing function. The role involves drafting clinical study protocols, regulatory documents, and managing review timelines within a collaborative team environment. Candidates...Hourly payFull timeContract workRemote work- ...following fields: Qualifications BA/MA/PhD related to Life Sciences Biomedical engineer Chemical Engineer Clinical Research Associate... ...Technician Lead Researcher/Principal Investigator Technical Writer Additional Information All information will be kept confidential...Biomedical
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