Senior Associate, Global Submission Management

Eisai•Nutley, NJ

About The Position

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai’s human health care (hhc) mission. We’re a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer’s disease. As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile, we want to hear from you. Support regulatory submission/publishing activities for eCTD global submission dossiers according to Agency and ICH Guidance requirements for major filings, (IND, NDA, sNDA, Amendments, DMFs, etc.) and regulatory maintenance activities. Support global submission timelines and coordination of publishing activities of work-related experience required for this position. Solid knowledge of submission requirements for regional markets may be required to ensure the overall submission and quality of the dossier meets regulatory compliance.

Requirements

Bachelor’s Degree required, preferably in science or health related discipline
Minimum 3-5 years pharma experience, including at least 1-2 years submission experience
Experience regulatory professional that understands regulatory submission/ePublishing requirements for filing original applications, amendments, complex supplements/variations and line extensions, as well as routine submissions.
Excellent communication skills required to interact effectively with regulatory affairs members and regulatory colleagues in gathering the necessary information required for submissions, and to proactively address sensitive issues with diplomacy and tact.
Applies good judgment and demonstrates initiative to resolve issues.
Advance understanding of Submission Project Management tools and techniques.
Ensures submissions are processed in accordance with established SOPs.
Excellent analytical and problem solving skills: facilitating team(s) to identify issues and propose solutions with respect to regulatory eCTD submission issue
Strong Communication Skills: Excellent verbal and written communication skills with demonstrated ability to present and articulate requirements with regulatory affairs members and regulatory colleagues proactively.
Ability to foster and maintain relationships with strategic global regulatory organization and other functional partners to ensure understanding of current processes.
Project Management Skills: Strong project management skills with attention to detail, ability to work in a fast-paced environment while successfully prioritizing and working on multiple tasks while utilizing organizational skills.
Regional Regulatory Submission Knowledge: US Specific: Familiarity with FDA & ICH Regulations & guidelines, IND, NDA, sNDA, Amendments, Annual Reports, Orphan Drugs, Module 1 - Cover letter, forms, labelling & SPL, administrative information, Module 4 – STF, Module 5 –STF related to IND and marketing applications.
Serve as the Subject Matter Expert (SME) regarding eCTD processes and procedures.
Knowledge of Drug Development: Experience in regulatory operations or regulatory affairs with advanced knowledge of pharmaceutical development (e.g. CMC, Nonclinical, Clinical)
Technology & Software Skills: Advanced working knowledge of global eCTD publishing and Electronic Document Management technology, ISI Toolbox, Regulatory Tracking Systems (RTS) and related technology applications. Advanced user skill in MS Word, MS Sharepoint, Adobe Acrobat Professional, eCTD content templates and experience.
Teamwork Skills: Experience in working on teams and to establish effective relationships with team members.
Critical Thinking and Problem Solving Skills: Ability to track regulatory eCTD submission changes (e.g. regional DTD upgrade or system upgrades) and interpret potential implications for regulatory activities, training and/or timelines. Ability to identify the root cause of problems as well as the implications associated with potential solutions and communicate to management.

Responsibilities

Manage assigned regulatory activity projects and closely collaborates with Senior Managers from GSM, Regulatory Affairs and other functional areas for the planning and publishing of regulatory submissions, monitoring submission forecast and ensuring timely high quality of regulatory submissions are submitted to health authority within required submission timelines.
Publishing regulatory submissions (bookmarks, hypertext links, QC) scheduled to be submitted to regulatory agencies (e.g., FDA, EMA and Health Canada).
Assists with hands-on daily submission compilation and publishing activities associated with preparation of various dossier types
Responsible for publishing, review, submission compilation and archive for routine regulatory activities (e.g. Amendments) and complex eCTD submissions (e.g. IND, NDA).
Uses internal and industry best practices in order to ensure quality submission deliverables.
Provide operational oversight to ensure timely, high quality regulatory submissions
Participates in the development of optimal business processes (internal guides, SOPs, etc.) and practices within the department to ensure high levels of customer support and to achieve high quality submissions.
Identifies and advises management with regards to opportunities for efficiencies, business process improvements, and cost reductions.
Position accountability/scope includes supervision of certain projects and assistance with priority setting required.
Receives project assignments from manager, but has the responsibility for independently managing and executing own projects.
Reviews project progress with manager on a regular basis with direction provided on follow-up.
Identifies opportunities and advises management for process improvements or cost savings.
May participate on internal project teams in order to guide and update business processes.
Supports various document management assignments, including file transfer, archiving, tracking, and archival of Regulatory submission documentation (including SPL, FDA correspondence and submission).
Demonstrates team leadership skills and ability to positively influence and work with others.
Builds and maintains positive relationships internally and externally.
Participates in other key projects and activities as assigned by management to support the Regulatory Operations function including submission authoring and Regulatory Systems implementation projects.
Assist with hands-on daily submission compilation and publishing activities associated with preparation of various regulatory submission types.
Applies good judgment and demonstrates initiative to resolve issues.
Expert understanding of Project Management tools and techniques.
Ensures publishing activities are processed in accordance with established SOPs.
Ability to demonstrate problem solving skills and facilitate team(s) to identify issues and propose solutions with respect to regulatory technical issues
Manage the submission timelines with Senior Managers and regulatory affairs representatives, maintains the submission timelines, collect status updates from the Publishing Manager and subteam members, RA Leads and reports submission status and activities to various stakeholders.
Provide metrics and project tracking to measure progress and keep project on track.
Collaborate timeline with the regulatory affairs representatives, maintains the submission timelines, obtain status updates from the Publishing Manager and subteam members, RA Leads and reports submission status and activities to various stakeholders.
Update the regulatory submission calendar, and reports on key submission milestones to stakeholders, as applicable.
Participate and contribute to new and updated process and procedures.
Review regulatory documents to ensure compliance with submission guidelines to drive efficient future state process including gaining buy in for key stakeholder and drive to standardization of processes.
Identifies risks and opportunities and addresses as needed with a focus on regulatory compliance requirements by supporting best practices, Working Procedures and SOPs.
Support process updates due to changing regulations that impact submission strategies and technologies, SEND, CDISC, Validator Software, etc.
This includes not limited to identifying the validation checks needed to ensure compliance with eCTD Specifications for world-wide regulatory agencies.
May participate on internal project teams in order to guide and update business processes, as applicable.
Support technology activities to ensure that regulatory information applications and systems are implemented, validated, and maintained in accordance with regulatory requirements compliance including but not limited to performing UAT scripts).
Support Global System development and process development on a basic level, and process redesign.
Technical knowledge of the US and global regulatory requirements for electronic submissions
Support and coordinate training to global submission management, regulatory publishing and other functional areas.
Perform and collect regulatory information applicable to global electronic submissions guidance, publishing tasks, data standards, and technology and marketing trends in regulatory space.
Ability to gather data, analyze research material information and communicate to management potential impact on regulatory operations strategies, and/or identify hot topic issues.
Responsible for staying abreast of US, Harmonized (ICH) eCTD and Global guidances, and provide updates as required

Benefits

Employees are eligible to participate in Company employee benefit programs.
For additional information on Company employee benefits programs, visit https://careers.eisai.com/us/en/compensation-and-benefits.
Certain other benefits may be available for this position, please discuss any questions with your recruiter.

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