Regulatory Publisher
5 days ago
Description:
- 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 – daily, weekly, or monthly
- 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-reference hyperlinks)
- Complete high-quality submissions following regulatory guidelines and internal processes within timeliness.
- Ensure consistency across regulatory submission documents following the regulatory style guide
- 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
- 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
- Good communication and organizational skills, as well as a high level of proficiency with problem-solving, conflict resolution, negotiation, and team-building skills
- 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
- Demonstrated ability and willingness to learn new products and processes independently and quickly
- Ability to work under deadlines to meet project timelines, including the ability to modify work schedules when needed
Required Experience and Qualifications:
- Minimum Bachelor’s degree or its equivalent
- 0 to 2 years experience in eCTD Regulatory Publishing
- Problem-solving abilities and adaptability
- Direct knowledge of or willingness to learn eCTD publishing tools. A rapid increase in eCTD document structure, system, & content knowledge is expected
- Technical writing and documentation knowledge
- Strong technical aptitude
- Confidence and assertiveness
Desired Experience and Skills
- Strong attention to detail, 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
-
Analyst III Regulatory Publishing
6 months ago
Hyderabad, India 2083 DXC Technology India Private Limited Full timeJob Description: • Successfully meet/ complete training milestones relevant to the position held. • Familiarity with FDA, GCPs, ICH guidelines, Life Sciences & Pharmaceutical industry • Familiarity of health authority procedures / guidance regarding electronic submissions • Perform submission publishing, assembly, and distribution activities...
-
Associate - Ra Publishing
4 months ago
Hyderabad, Telangana, India Makrocare Full time**Job Summary**: **Key Responsibilities**: - Prepare, review, and compile regulatory submissions in eCTD/aCTD formats for various markets including the US, UK, EU, and ROW. - Ensure submissions are compliant with the regulatory guidelines and are ready for on-time dispatch. - Manage and track the status of submissions and respond to regulatory agencies'...
-
Associate - Ra Publishing
4 months ago
Hyderabad, Telangana, India MAKRO Full time**Job Summary**: **Key Responsibilities**: Prepare, review, and compile regulatory submissions in eCTD/aCTD formats for various markets including the US, UK, EU, and ROW. Ensure submissions are compliant with the regulatory guidelines and are ready for on-time dispatch. Manage and track the status of submissions and respond to regulatory agencies' queries...
-
Associate - RA Publishing
4 months ago
Hyderabad, India Makro Full timePosition:Associate RAPublishingLocation:Hyderabad Madhapur Telangana500081ExperienceRequired: 13YearsEducation:Bachelor s Degree in Life Sciences or relatedfieldMarkets:US/UK/EU/ROWJobSummary:We are seeking adetailoriented and proactive Associate Regulatory Affairs (RA)Publishing with 13 years of experiencein regulatory submissions across global markets...
-
Global Clinical Publishing Associate
6 months ago
Hyderabad, Telangana, India Novartis Full time**Summary**: Ensure compliance with internal and external guidelines, to compile and add electronic navigation to clinical and regulatory documents. Support the timely submission of documents to the Health Authorities (HAs) and provide publishing consultancy to the clinical teams and other line functions. **About the Role**: **Major accountabilities**: -...
-
Associate, Regulatory Affairs
1 month ago
Hyderabad, India SteriMax Inc. Full timePosition Title:Associate, Regulatory AffairsReports To:Director, Regulatory AffairsLocation:Hyderabad, Telangana, IndiaPOSITION DESCRIPTIONThe RA Associate will prepare regulatory submissions for generic drug products and actively participate in the management of submissions under regulatory agency review to fulfill Canadian regulatory requirements.KEY...
-
Associate, Regulatory Affairs
1 month ago
hyderabad, India SteriMax Inc. Full timePosition Title: Associate, Regulatory Affairs Reports To: Director, Regulatory Affairs Location: Hyderabad, Telangana, India POSITION DESCRIPTION The RA Associate will prepare regulatory submissions for generic drug products and actively participate in the management of submissions under regulatory agency review to fulfill Canadian regulatory...
-
Associate, regulatory affairs
1 month ago
Hyderabad, India SteriMax Inc. Full timePosition Title: Associate, Regulatory Affairs Reports To: Director, Regulatory Affairs Location: Hyderabad, Telangana, India POSITION DESCRIPTION The RA Associate will prepare regulatory submissions for generic drug products and actively participate in the management of submissions under regulatory agency review to fulfill Canadian regulatory...
-
Associate, Regulatory Affairs
2 weeks ago
Hyderabad, India SteriMax Inc. Full timePosition Title: Associate, Regulatory Affairs Reports To: Director, Regulatory AffairsLocation: Hyderabad, Telangana, IndiaPOSITION DESCRIPTIONThe RA Associate will prepare regulatory submissions for generic drug products and actively participate in the management of submissions under regulatory agency review to fulfill Canadian regulatory...
-
Associate, Regulatory Affairs
1 month ago
hyderabad, India SteriMax Inc. Full timePosition Title: Associate, Regulatory AffairsReports To: Director, Regulatory AffairsLocation: Hyderabad, Telangana, IndiaPOSITION DESCRIPTIONThe RA Associate will prepare regulatory submissions for generic drug products and actively participate in the management of submissions under regulatory agency review to fulfill Canadian regulatory requirements.KEY...
-
Associate, regulatory affairs
1 month ago
Hyderabad, India SteriMax Inc. Full timePosition Title: Associate, Regulatory AffairsReports To: Director, Regulatory AffairsLocation: Hyderabad, Telangana, IndiaPOSITION DESCRIPTIONThe RA Associate will prepare regulatory submissions for generic drug products and actively participate in the management of submissions under regulatory agency review to fulfill Canadian regulatory requirements.KEY...
-
Associate, Regulatory Affairs
1 month ago
Hyderabad, India SteriMax Inc. Full timePosition Title: Associate, Regulatory AffairsReports To: Director, Regulatory AffairsLocation: Hyderabad, Telangana, India POSITION DESCRIPTIONThe RA Associate will prepare regulatory submissions for generic drug products and actively participate in the management of submissions under regulatory agency review to fulfill Canadian regulatory requirements. KEY...
-
Associate, Regulatory Affairs
1 month ago
Hyderabad, India SteriMax Inc. Full timePosition Title: Associate, Regulatory Affairs Reports To: Director, Regulatory Affairs Location: Hyderabad, Telangana, India POSITION DESCRIPTION The RA Associate will prepare regulatory submissions for generic drug products and actively participate in the management of submissions under regulatory agency review to fulfill Canadian regulatory...
-
Associate, Regulatory Affairs
1 month ago
hyderabad, India SteriMax Inc. Full timePosition Title: Associate, Regulatory Affairs Reports To: Director, Regulatory Affairs Location: Hyderabad, Telangana, India POSITION DESCRIPTION The RA Associate will prepare regulatory submissions for generic drug products and actively participate in the management of submissions under regulatory agency review to fulfill Canadian regulatory...
-
Associate, Regulatory Affairs
1 month ago
hyderabad, India SteriMax Inc. Full timePosition Title: Associate, Regulatory AffairsReports To: Director, Regulatory AffairsLocation: Hyderabad, Telangana, India POSITION DESCRIPTIONThe RA Associate will prepare regulatory submissions for generic drug products and actively participate in the management of submissions under regulatory agency review to fulfill Canadian regulatory requirements. KEY...
-
Associate, Regulatory Affairs
1 month ago
Hyderabad, India SteriMax Inc. Full timePosition Title: Associate, Regulatory AffairsReports To: Director, Regulatory AffairsLocation: Hyderabad, Telangana, India POSITION DESCRIPTIONThe RA Associate will prepare regulatory submissions for generic drug products and actively participate in the management of submissions under regulatory agency review to fulfill Canadian regulatory requirements. KEY...
-
Hyderabad, Telangana, India Novartis Full time**Summary**: - Ensures a controlled documentation system, record retention, and information services including electronic records retention processes in accordance with regulatory requirements. Ensures compliance to the requirements from regulatory agencies. Maintains the technical and non-technical documentation change system. Assures procedures are in...
-
Regulatory Submission Professional
4 weeks ago
Hyderabad, Telangana, India Bristol Myers Squibb Full timeBristol Myers Squibb is a leading global biopharmaceutical company that transforms patients' lives through science and innovation.We are committed to creating a diverse and inclusive work environment where our employees can grow and thrive.As a Senior Submission Specialist at Bristol Myers Squibb, you will play a critical role in delivering Health Authority...
-
High Salary: Associate, Regulatory Affairs
1 month ago
Hyderabad, India SteriMax Inc. Full timePosition Title: Associate, Regulatory AffairsReports To: Director, Regulatory AffairsLocation: Hyderabad, Telangana, IndiaPOSITION DESCRIPTIONThe RA Associate will prepare regulatory submissions for generic drug products and actively participate in the management of submissions under regulatory agency review to fulfill Canadian regulatory requirements.KEY...
-
Regulatory Affairs Specialist
1 week ago
Hyderabad, Telangana, India SteriMax Inc. Full timeWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at SteriMax Inc.About the RoleAs a Regulatory Affairs Specialist, you will play a crucial role in preparing regulatory submissions for generic drug products and actively participating in the management of submissions under regulatory agency review to fulfill Canadian regulatory...