Medical Writer

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🕒 vor 29 Tagen

🌵 Arizona, Connecticut, +10 weitere Bundesländer – Remote

🌵 Arizona – Remote 🦌 Connecticut – Remote 🐊 Florida – Remote 🌽 Illinois – Remote 🗻 New Hampshire – Remote 🏖️ New Jersey – Remote 🌲 North Carolina – Remote 🍂 Massachusetts – Remote 🏰 Missouri – Remote 🔔 Pennsylvania – Remote ⛷️ Utah – Remote ⚔️ Virginia – Remote

💵 $65.305 - $93.000 / Jahr

⏰ Vollzeit

🟡 Mittelstufe

🟠 Senior

🏥📝 Medizinischer Autor

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Perceptive Inc.

WebsiteLinkedInAlle Stellen

1001 - 5000 Mitarbeiter

🏥 Gesundheitswesen

💼 Beratung

📦 Logistik

Healthcare • Consulting • Logistics

Perceptive Inc. ist ein führender Anbieter von wissenschaftlichen und datenbasierten Lösungen für die biopharmazeutische Industrie, mit Schwerpunkt auf Onkologie, therapeutischen Bereichen des zentralen Nervensystems (ZNS) und muskuloskelettaler Bildgebung. Mit Expertise in der Wirkstoffforschung, präklinischer und früher klinischer Bildgebung sowie Radiochemie bietet Perceptive Dienstleistungen, die vielversprechende Wirkstoffkandidaten identifizieren und Risiken durch erstklassige Bildgebungsdienste mindern. Darüber hinaus bietet es umfassende eClinical-Lösungen, einschließlich Randomisierung und Versorgungsmanagement für Studien (RTSM), die darauf abzielen, klinische Studienprozesse zu optimieren. Perceptive gilt als zuverlässiger Partner beim Vorantreiben klinischer Studien und der schnelleren Bereitstellung essenzieller Behandlungen für Patienten, gestützt auf über 50 Jahre Erfahrung und ein Team engagierter Experten. Die weltweite Präsenz von Perceptive gewährleistet eine nahtlose Bereitstellung von Discovery-, eClinical- und Bildgebungsdiensten zur Unterstützung klinischer Studien auf globaler Ebene.

Beschreibung

• Create, research, edit and coordinate the production of clinical documents related to independent review • Gather, review, analyze, and evaluate relevant resources to prepare, develop, and finalize applicable clinical documents for submission to regulatory authorities • Prepare, develop, and finalize applicable clinical documents not intended for submission to regulatory authorities • Revise document drafts based on the review comments from team members to ensure inclusion of all relevant input • Follow required standard operating procedures (SOPs), templates, guidelines, regulations, client instructions, and other processes, as applicable • Perform literature searches/reviews as necessary to obtain background information and training for development of documents • Draft and/or ghost-write clinical documents for more experienced medical writers • Serve as primary client contact for medical writing projects, negotiating deliverable timelines, and resolving project-related issues • Serve as the medical writing representative on assigned project teams communicate content requirements • Coordinate and conduct interdepartmental team reviews of draft and final documents • Evaluate progress on tasks, identify issues and facilitate resolutions, and advance document development to approval, according to Calyx and/or client guidelines/SOPs • Distribute final documents to project team and client in a timely manner and to agreed timescales • Identify potential project challenges and raise with all relevant stakeholders, including changes in timelines or out of scope requests, and suggest possible resolution options • Ensure appropriate filing of applicable project documentation • Use appropriate methods and a systematic approach in the development, maintenance, control and distribution of documents • Prepare documents for publishing readiness, ensuring document consistency and integrity • Ensure documentation adheres to FDA/EMA or other appropriate regulatory guidelines, and / or relevant SOPs • Provide medical editing review of draft and final documents prepared by other medical writers before internal or external distribution

🎯 Anforderungen

• Excellent interpersonal, verbal, presentational and written communication skills • Ability to consistently produce documents of high quality • A flexible attitude with respect to work assignments and new learning • Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail • Must have the ability to work methodically in a fast-paced, time-sensitive environment • Demonstratable ability to apply critical thinking to problems and tasks • Shows initiative and self-confidence, is adaptable and is able to cope with changing and evolving priorities • Ability to identify and implement process improvements • Proactively participates in skills improvement training and encourages their teams to participate • Maintains an up-to-date awareness of trends, tools, technology, techniques, processes and documentation requirements that affect technology within the Life sciences domain • A self-starter and able to work under own initiative • Extensive clinical/scientific writing skills. • Proven ability of using Microsoft Office products (including Word, Excel & PowerPoint) • Experience using tools to communicate progress to Stakeholders • Experience of regulated environments • Understanding of Agile methodologies • Experience of working in and knowledge of the life sciences sector • Solid knowledge of industry guidelines and regulations, i.e., ICH-GCP. • Experience of regulatory documents in a contract research organization, pharmaceutical or biotechnology firm, or some experience in the conduct of clinical research/medical communications. • Solid Professional experience in the same or very similar role • Bachelor's Degree in a technical discipline (Science, pharmacy, nursing, or other health-related discipline preferred etc.) or a related study, or equivalent project-related experience • Fluent in English (written and verbal)

🏖️ Vorteile

• Medical, Dental and Vision benefits for you and your family, including Flexible Spending Accounts (FSA) and Health Savings Accounts (HSAs) • Paid time off policy including holidays and sick time • Internal growth and development programs & trainings • 401(k) program, life & accident insurance and disability insurance