Senior Medical Writer – Regulatory

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🕒 vor 16 Tagen

🦀 Maryland – Remote

🦀 Maryland – Remote

💵 $80.600 - $175.700 / Jahr

⏰ Vollzeit

🟠 Senior

🏥📝 Medizinischer Autor

🦅 H1B-Visum-Sponsor

Dieses Unternehmen hat in der Vergangenheit H1B-Visa gesponsert.

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Syneos Health

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10.000+ Mitarbeiter

🏥 Gesundheitswesen

💼 Beratung

📦 Logistik

Healthcare • Consulting • Logistics

Syneos Health ist eine führende, vollständig integrierte biopharmazeutische Lösungsorganisation, die darauf ausgelegt ist, den Erfolg ihrer Kunden zu beschleunigen. Sie übersetzen einzigartige klinische, medizinische und kommerzielle Erkenntnisse in Ergebnisse, um den Anforderungen des modernen Marktes gerecht zu werden. Durch die Nutzung fortschrittlicher Technologien und Erkenntnisse arbeitet Syneos Health mit Kunden zusammen, um die Bereitstellung wichtiger Therapien für Patienten weltweit zu beschleunigen, und bietet Dienstleistungen, die das gesamte Spektrum von der klinischen Entwicklung bis zur Kommerzialisierung abdecken.

Beschreibung

• Manage medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision • Completes required administrative tasks within the specified timeframes • Performs online clinical literature searches and complies with copyright requirements • Develops deep expertise on key topics in the industry and the regulatory requirements and guidelines that affect medical writing • Minimal travel may be required (less than 25%)

🎯 Anforderungen

• Leads the clear and accurate completion of medical writing deliverables, ensuring scientific information is presented clearly and accurately • Completes a variety of documents that may include clinical study protocols and clinical study protocol amendments; clinical study reports; patient narratives; annual reports; investigator brochures; informed consents; annual reports; plain language summaries; periodic safety update reports, clinical development plans; IND submissions; integrated summary reports; NDA and eCTD submissions; journal manuscripts; and abstracts, posters, and presentations for scientific meetings • Adheres to established regulatory standards, including, but not limited to, ICH E3 guidelines, as well as company standard operating procedures, client standards, and company and/or client approved-templates, authorship requirements, and style and formatting guides, when completing medical writing projects, on time and on budget • Coordinates quality and editorial reviews • Acts as peer reviewer for internal team to ensure document scientific content, clarity, overall consistency, and proper format • Reviews statistical analysis plans and table/figure/listing specifications for appropriate content, and for grammar, format, and consistency • Interacts and builds good working relations with clients, department head, and peers in data management, biostatistics, regulatory affairs, and medical affairs, as necessary, to produce writing deliverables • Identifies and proposes solutions to resolve issues • Mentors and leads less experienced medical writers on complex projects, as necessary

🏖️ Vorteile

• Health benefits to include Medical, Dental and Vision • Company match 401k • Eligibility to participate in Employee Stock Purchase Plan • Eligibility to earn commissions/bonus based on company and individual performance • Flexible paid time off (PTO) and sick time