Medical Writing Word Processing Coordinator

Synectics Inc.; United States; Presencial; USD 65 000 - 90 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Healthcare Insurance

Dental Insurance

Vision Insurance

401(k) Plan

Equal opportunity employer

Resumo da oferta

Synectics Inc. is seeking a Medical Writing Operations Formatter to format and review submission-ready documents and support CSR Appendices coordination within RIMS.

The role partners with Medical Writers and cross-functional teams to ensure documents meet formatting standards and regulatory requirements, while adhering to project timelines and CSR/CTD structure.

Qualificações

• Bachelor's degree in English or Communications required.
• 3–5 years of relevant pharmaceutical industry experience in medical writing, quality, regulatory, clinical research, or product support/R&D desired.

Responsabilidades

• Format, review, and maintain submission-ready documents.
• Coordinate CSR Appendices within Regulatory Information Management Systems (RIMS).
• Ensure document formats comply with regulatory templates and eSubmissions standards.
• Publish documents in RIMS and manage timelines for word processing and submissions.

Conhecimentos

Interpersonal communication

Organizational communication

Conflict management

Formação académica

Bachelor's degree in English or Communications

Descrição da oferta de emprego

Job Description

• The Medical Writing Operations Formatter provides document formatting and Clinical Study Report (CSR) Appendix support for clinical and regulatory documents.
• This role partners closely with Medical Writers and cross-functional stakeholders to ensure documents meet established formatting standards, regulatory requirements, and project timelines.
• The formatter is responsible for formatting, reviewing, and maintaining high-quality submission-ready documents and supporting CSR Appendix coordination activities within Regulatory Information Management Systems (RIMS).
• Defines scope of formatting, or Clinical Study Reports (CSR) Appendices activities with the document author.
• Format, import and route documents in the regulatory information management systems (RIMS).
• Ensure document format and styles are consistent with the defined in RIMS and are consistent with the clinical and regulatory templates.
• Ensure document properties and naming conventions are used.
• Maintain strong knowledge of RIMS styes and formatting standards.
• Ensures all documents are published in RIMS and meet required timelines.
• Ensure completeness of information in CSR Appendices.
• Maintain strong knowledge of CSR/CSR appendices organization and content and knowledge of CTD structure.
• Contributes to the development, implementation, and maintenance of medical writing operations business processes.
• Acts as subject matter expert (SME) for the master file system and formatting, report publishing, or Clinical Study Reports (CSR) Appendices to the medical writing stakeholders.
• Effectively communicates deliverables needed to stakeholders.
• Must demonstrate good interpersonal and organizational communication skills, including conflict management skills.
• Assists in the management of the centralized mailbox.
• Tracks and maintains metrics and assists in the preparation and maintenance of training documents.
• Processes, proofreads, verifies and manages various clinical regulatory documents, ensuring they are submission-ready for publishing with an appropriate level of accuracy and consistency.
• Communicates regularly with colleagues and management regarding timelines and conflict to timelines for word processing requests, eSubmissions issues, and document completion dates.
• Provides ongoing support for Medical Writing, Clinical, and, other functional areas; acts as a liaison between eDocs support and Medical Writing as needed.
• Responsible for effective communication among team members.
• Ensures all electronic document deliverables are processed and completed in alignment with timelines.
• Accountable for meeting the main objectives of assigned word processing projects within established timelines and with an appropriate quality level.
• Ensures document styles and formatting are consistent with defined eSubmissions standards, so that documents created in MS Word are correctly rendered to PDFs.
• Confirms formats and styles are consistent with those in the clinical regulatory templates, when applicable.
• Accountable for providing services and results on time, accurately and consistent with expectations.
• Populates document properties and ensures correct naming conventions are used per the eSubmissions System file naming conventions.
• Accurately and timely maintains document tracking for all documents.
• Ensures literature citations are correct.
• Performs literature searches.
• Maintains knowledge of eSubmissions styles and formatting standards.
• Must continually train/be compliant with all current industry requirements as they relate to regulatory submissions, including electronic submission/approval standards.
• Participates in process improvement activities.

Qualifications

• Bachelor of Science or Bachelor's degree in English or Communications will be considered.
• 3 to 5 years of relevant pharmaceutical industry experience in a related area such as medical writing, quality, regulatory, clinical research, or product support/Research & Development desired.

Benefits

Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics.

Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.

Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.

401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first of the month following at least 1 calendar year after employment begins.

Synectics is an equal opportunity employer.