TransPerfect | Senior Regulatory Publisher
2 weeks ago
The Senior Regulatory Publisher is responsible for working with Regulatory Affairs to publish Clinical Study Reports, IND documents, NDA documents, and other regulatory documents according to ICH, eCTD, and other applicable electronic publishing standards, as well as to prepare, assemble and submit applications (IND/CTA/NDA/MAA/NDA, etc.) for submission to ensure compliance with government acts and regulations. This position also requires the employee to implement publishing processes across multiple teams.
DESCRIPTION
Report directly to the Team Manager on all team and client issues, project work, project deliverables associated timelines, ensuring SLAs are satisfied and deliver reporting – daily, weekly, or monthly
Publish Clinical Study Reports, IND documents, NDA documents, and other regulatory documents according to ICH, eCTD, and other applicable electronic publishing standards
Develop a thorough understanding of all aspects of the publishing software, tools, process, and output requirements
Perform eCTD readiness/pre-publishing tasks (i.e., formatting, bookmarking, and document navigation) Perform tasks within the publishing system (creating eCTD submissions, lifecycle management, assigning documents, adding cross-references hyperlinks)
Complete high-quality submissions following regulatory guidelines and internal processes within timelines
Ensure consistency across regulatory submission documents following the regulatory style guide
Perform publishing QC tasks within the electronic publishing system and QC of the published output to ensure high submission quality
Perform document quality control checks for others in the department, promptly communicating irregularities in documents and coordinating issue resolution
Maintain knowledge of current regional regulations in regard to application format
Understand, interpret, and apply Agency regulations and guidelines related to eCTD submissions
Dispatch submissions to Regulatory Authorities via agency portal, through customers or directly
Build a good working partnership with Service Desk and Solutions Engineering Teams to ensure efficiency for project deliverables and timelines are adhered and SLAs are kept
Participate in submission team meetings to plan and track submissions and relevant documents as assigned
Periodically perform review of the process to find any process gaps and feedback to the team for improvement of the process
Attend client meetings as needed, and represent the TI team as a Regulatory Publishing Subject Matter Expert (SME) as requested
Develop understanding and maintain knowledge of appropriate standard operating procedures (SOPs), regulations, policies, and regulatory guidance documents
Complete all other tasks that are deemed appropriate for this role and assigned by the manager/supervisor
REQUIRED SKILLS
Demonstrate attention to detail
Ability to successfully train & learn under the more advanced Specialists on how to conduct all quality assurance reviews in the specified areas
Ability to prioritize critical needs, act decisively, and handle a high volume of complex tasks within a given timeframe
Excellent communication and organizational skills, as well as a high level of proficiency with problem-solving, conflict resolution, negotiation, and team-building skills
Take a proactive role in learning about clients’ industry and business needs and company culture, communicating with the Configuration Team, and providing a high level of service
Highly proficient computer skills including Adobe Acrobat DC and MS Word, Electronic submission software, Windows and MS Office (Outlook, Word, Excel, PowerPoint, SharePoint) or similar software.
Ability to work under deadlines to meet project timelines, including the ability to modify work schedules when needed.
Demonstrated ability and willingness to learn new products and processes independently and quickly.
REQUIRED EXPERIENCE AND QUALIFICATION
Minimum Bachelor’s degree or its equivalent
4+ years’ experience in eCTD Regulatory Publishing required
Direct knowledge of or willingness to learn eCTD publishing tools
Problem-solving abilities and adaptability
Technical writing and documentation knowledge
Strong technical aptitude
Confidence and assertiveness
DESIRED SKILLS AND EXPERIENCE
Strong attention to detail, organization, multitasking, project management, teamwork, and communication skills
Adaptable / Flexible approach to work
Self-starter with excellent organization and time management skills
Result-oriented, biased to action.
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Pune, India TransPerfect Full timeOVERVIEW The Senior Regulatory Publisher is responsible for working with Regulatory Affairs to publish Clinical Study Reports, IND documents, NDA documents, and other regulatory documents according to ICH, eCTD, and other applicable electronic publishing standards, as well as to prepare, assemble and submit applications (IND/CTA/NDA/MAA/NDA, etc.) for...
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Pune, India TransPerfect Full timeOVERVIEWThe Senior Regulatory Publisher is responsible for working with Regulatory Affairs to publish Clinical Study Reports, IND documents, NDA documents, and other regulatory documents according to ICH, eCTD, and other applicable electronic publishing standards, as well as to prepare, assemble and submit applications (IND/CTA/NDA/MAA/NDA, etc.) for...
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Pune, India TransPerfect Full timeOVERVIEW The Senior Regulatory Publisher is responsible for working with Regulatory Affairs to publish Clinical Study Reports, IND documents, NDA documents, and other regulatory documents according to ICH, eCTD, and other applicable electronic publishing standards, as well as to prepare, assemble and submit applications (IND/CTA/NDA/MAA/NDA, etc.) for...
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Senior Regulatory Publisher
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Pune, India TransPerfect Full timeDescription:Report directly to the Team Manager on all team and client issues, project work, project deliverables associated timelines, ensuring SLAs are satisfied and deliver reporting – daily, weekly, or monthlyPublish Clinical Study Reports, IND documents, NDA documents, and other regulatory documents according to ICH, eCTD, and other applicable...
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Pune, India TransPerfect Full timeDescription: Publish Clinical Study Reports, IND documents, NDA documents, and other regulatory documents according to ICH, eCTD, and other applicable electronic publishing standards Report directly to the Team Manager on all team and client issues, project work, project deliverables associated timelines, ensuring SLAs are satisfied and deliver reporting...
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Pune, India TransPerfect Full timeOVERVIEW The Regulatory Publisher I is responsible for working with Regulatory Affairs to publish Clinical Study Reports, IND documents, NDA documents, and other regulatory documents according to ICH, e CTD, and other applicable electronic publishing standards, as well as to prepare, assemble, and submit applications (IND/CTA/NDA/MAA/NDA, etc.) for...
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Regulatory publisher ii
2 weeks ago
Pune, India TransPerfect Full timeOVERVIEWThe Regulatory Publisher II is responsible for working with Regulatory Affairs to publish Clinical Study Reports, IND documents, NDA documents, and other regulatory documents according to ICH, e CTD, and other applicable electronic publishing standards, as well as to prepare, assemble and submit applications (IND/CTA/NDA/MAA/NDA, etc.) for submission...
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Regulatory Publisher II
2 weeks ago
Pune, India TransPerfect Full timeOVERVIEWThe Regulatory Publisher II is responsible for working with Regulatory Affairs to publish Clinical Study Reports, IND documents, NDA documents, and other regulatory documents according to ICH, eCTD, and other applicable electronic publishing standards, as well as to prepare, assemble and submit applications (IND/CTA/NDA/MAA/NDA, etc.) for submission...
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Regulatory Publisher II
2 weeks ago
Pune, India TransPerfect Full timeOVERVIEW The Regulatory Publisher II is responsible for working with Regulatory Affairs to publish Clinical Study Reports, IND documents, NDA documents, and other regulatory documents according to ICH, eCTD, and other applicable electronic publishing standards, as well as to prepare, assemble and submit applications (IND/CTA/NDA/MAA/NDA, etc.) for...
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Regulatory Publisher I
2 weeks ago
Pune, India TransPerfect Full timeOVERVIEWThe Regulatory Publisher I is responsible for working with Regulatory Affairs to publish Clinical Study Reports, IND documents, NDA documents, and other regulatory documents according to ICH, eCTD, and other applicable electronic publishing standards, as well as to prepare, assemble, and submit applications (IND/CTA/NDA/MAA/NDA, etc.) for submission...