Curium Pharma
Regulatory Affairs Specialist - Publishing
Curium Pharma, Maryland Heights, Missouri, United States, 63043
Regulatory Affairs Specialist – Publishing
Date: Dec 11, 2025
Location: St. Louis, MO, United States, 63146
About Curium Curium is the world's largest nuclear medicine company with more than a century of industry experience. We develop, manufacture and distribute world‑class radiopharmaceutical products to help patients around the globe. Our proven heritage combined with a pioneering approach delivers innovation, excellence and unparalleled service.
With manufacturing facilities across Europe and the United States, Curium delivers SPECT, PET and therapeutic radiopharmaceutical solutions for life‑threatening diseases to over 14 million patients annually. The name “Curium” honors the legacy of pioneering radioactive researchers Marie and Pierre Curie, after whom the radioactive element curium was named and emphasizes our focus on nuclear medicine. The tagline “Life Forward” represents our commitment to securing a brighter future for all those we serve: an enhanced quality of care for our patients, a trusted partner to our customers and a supportive employer to our valued team.
Summary of Position The Regulatory Affairs Specialist – Publishing leads the electronic publishing process and provides end‑to‑end submission support to the North America regulatory team. This includes formatting, compiling and publishing submission‑ready documents into compliant eCTD sequences for INDs, DMFs, BLAs, NDAs, ANDAs and other regulatory applications. The Specialist serves as the primary publisher for the US and Canadian Regulatory Affairs teams, collaborating closely with authors and project teams to ensure timely, high‑quality submissions to health authorities.
Work Schedule:
Monday – Friday 8:00 am – 4:30 pm
Essential Functions
Format MS Word and Adobe PDF files to be submission‑ready according to department standards and health authority requirements.
Create hyperlinks and bookmarks within and across documents/sections.
Compile, validate and publish eCTD sequences, ensuring accurate metadata and structure.
Coordinate publishing timelines with RA team and other stakeholders to meet project deadlines.
Maintain records and correspondence in the regulatory tracking system.
Provide guidance and training to authors on document formatting, submission standards and lifecycle updates.
Identify and implement process improvements to enhance publishing efficiency and quality.
Troubleshoot and resolve technical publishing issues, escalating when necessary.
Stay informed on updates to FDA, ICH and eCTD guidance.
Maintain operational compliance with US and international regulatory agencies and guidelines (FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.).
Requirements
Bachelor's degree in a relevant field of study.
1–3 years of hands‑on experience with publishing and compiling eCTD submissions using publishing tools (e.g., Lorenz DocuBridge, Extedo or similar). Experience with electronic submission publishing software and applications.
Knowledge of FDA, ICH and Health Canada submission requirements preferred.
Excellent communication, interpersonal, time‑management and organizational skills.
Close attention to detail.
Ability to work autonomously under limited direction on multiple projects simultaneously.
Demonstrates a working knowledge of publishing technologies/software.
All employees must read, write and speak fluent English.
Working Conditions
This position will work in typical office conditions with extensive time using computer equipment.
Willingness to work in a team‑based environment.
May be required to sit or stand for long periods of 8+ hours a day while performing duties.
Must possess good hand‑eye coordination.
Willingness to complete safety training within allotted timeframes.
Disclaimer The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.
Equal Opportunity Employer Curium is an equal opportunity employer and believes everyone deserves respect, dignity and equality. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
Job Segment Regulatory Affairs, Compliance, Medical Technologist, Law, Nuclear, Legal, Healthcare, Energy
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Location: St. Louis, MO, United States, 63146
About Curium Curium is the world's largest nuclear medicine company with more than a century of industry experience. We develop, manufacture and distribute world‑class radiopharmaceutical products to help patients around the globe. Our proven heritage combined with a pioneering approach delivers innovation, excellence and unparalleled service.
With manufacturing facilities across Europe and the United States, Curium delivers SPECT, PET and therapeutic radiopharmaceutical solutions for life‑threatening diseases to over 14 million patients annually. The name “Curium” honors the legacy of pioneering radioactive researchers Marie and Pierre Curie, after whom the radioactive element curium was named and emphasizes our focus on nuclear medicine. The tagline “Life Forward” represents our commitment to securing a brighter future for all those we serve: an enhanced quality of care for our patients, a trusted partner to our customers and a supportive employer to our valued team.
Summary of Position The Regulatory Affairs Specialist – Publishing leads the electronic publishing process and provides end‑to‑end submission support to the North America regulatory team. This includes formatting, compiling and publishing submission‑ready documents into compliant eCTD sequences for INDs, DMFs, BLAs, NDAs, ANDAs and other regulatory applications. The Specialist serves as the primary publisher for the US and Canadian Regulatory Affairs teams, collaborating closely with authors and project teams to ensure timely, high‑quality submissions to health authorities.
Work Schedule:
Monday – Friday 8:00 am – 4:30 pm
Essential Functions
Format MS Word and Adobe PDF files to be submission‑ready according to department standards and health authority requirements.
Create hyperlinks and bookmarks within and across documents/sections.
Compile, validate and publish eCTD sequences, ensuring accurate metadata and structure.
Coordinate publishing timelines with RA team and other stakeholders to meet project deadlines.
Maintain records and correspondence in the regulatory tracking system.
Provide guidance and training to authors on document formatting, submission standards and lifecycle updates.
Identify and implement process improvements to enhance publishing efficiency and quality.
Troubleshoot and resolve technical publishing issues, escalating when necessary.
Stay informed on updates to FDA, ICH and eCTD guidance.
Maintain operational compliance with US and international regulatory agencies and guidelines (FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.).
Requirements
Bachelor's degree in a relevant field of study.
1–3 years of hands‑on experience with publishing and compiling eCTD submissions using publishing tools (e.g., Lorenz DocuBridge, Extedo or similar). Experience with electronic submission publishing software and applications.
Knowledge of FDA, ICH and Health Canada submission requirements preferred.
Excellent communication, interpersonal, time‑management and organizational skills.
Close attention to detail.
Ability to work autonomously under limited direction on multiple projects simultaneously.
Demonstrates a working knowledge of publishing technologies/software.
All employees must read, write and speak fluent English.
Working Conditions
This position will work in typical office conditions with extensive time using computer equipment.
Willingness to work in a team‑based environment.
May be required to sit or stand for long periods of 8+ hours a day while performing duties.
Must possess good hand‑eye coordination.
Willingness to complete safety training within allotted timeframes.
Disclaimer The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.
Equal Opportunity Employer Curium is an equal opportunity employer and believes everyone deserves respect, dignity and equality. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
Job Segment Regulatory Affairs, Compliance, Medical Technologist, Law, Nuclear, Legal, Healthcare, Energy
#J-18808-Ljbffr