The Role
The Regulatory Operations Global Publishing Manager is responsible for overseeing the planning, creation, and submission of regulatory submissions. In collaboration with the Regulatory Lead, you will manage and prepare high-quality global submissions, both in-house and via CROs, ensuring timely delivery of compliant submissions to global health authorities. The Global Publishing Manager provides regulatory operations expertise to cross-functional submission project teams, promoting and ensuring excellence in the planning, preparation, and delivery of regulatory submissions. You will act as the primary point of contact for daily submissions for major submissions and lead a team of publishing specialists. At Moderna, we act with urgency and behave like owners, reflecting our commitment to delivering transformative medicines to patients.
Here’s What You’ll Do:
Compile, publish, and verify submission dossiers in accordance with international eCTD requirements.
Act as a team leader, providing direction, support, and mentorship to the publishing team.
Oversee the compilation, publishing, and verification of submission dossiers in accordance with international eCTD requirements and regulatory guidelines.
Lead and manage the submission of MAA, INDs, NDAs, BLAs, Master Files, and other regulatory documents.
Work closely with team members to compile documents, review hypertext links, ensure PDFs are submission ready, format tables and graphics, bookmark sections, and proof submissions according to internal standards.
Develop and implement new processes and procedures to enhance efficiency and accuracy during the submission process.
Collaborate with submissions management to build technically valid and high-quality dossiers.
Manage the submission of eCTD sequences through health authority gateways.
Perform quality control (QC) of documents published by team members to ensure compliance with applicable guidance documents.
Assist with the remediation of Word documents to ensure proper format and compliance.
Mentor and train team members to increase the quality across the team.
Participate in internal and external audits, maintaining compliance with department systems, e.g., project database, timesheets, training.
Contribute to the development of new publishing services and actively participate in department initiatives and process improvements.
Maintain a strong understanding of applicable regulatory guidelines and ensure the achievement of individual and team utilization targets.
Act as the primary point of contact for the team, providing regular updates to senior management on project status and any issues affecting quality, timelines, and adherence to contractual obligations.
Here’s What You’ll Bring to the Table:
Bachelor’s degree or equivalent.
At least 5 years of experience as a regulatory Publisher in a pharmaceutical company or CRO, with 2+ years in a management role.
Experience leading the submission of MAA, INDs, NDAs, BLAs, Master Files, etc., formatted according to international eCTD requirements.
Clinical report and global submission dossier publishing/compilation experience in the pharmaceutical or related industry.
Experience with electronic clinical document publishing standards/formats and global regulatory submission publishing standards/formats (e.g., eCTD, EU CTR).
Working knowledge of publishing tools (e.g., DXC, eCTD Xpress, Veeva), global submission validation tools, Document Management systems, Toolbox, HA electronic submission gateways, IRIS, CTIS, MS Office tools.
Familiarity with global Clinical and Regulatory HA requirements (e.g., FDA, ICH, EMA, MENA region, CH, MHRA).
Strong interpersonal and project management skills, with experience working in a complex, global cross-functional organization.
Highly motivated, organized, and detail-oriented team player.
Analytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines.
Ability to readily adjust to change in a fast-paced environment and multitask.
Positive attitude and ability to effectively collaborate with peers, stakeholders, and cross-functional colleagues in a global team environment.
Strong technical skills.
Strong communication and business writing skills.
Fluency in English.
This role is based in our new LEED-certified HQ in Cambridge, MA and is expected to be in office 70% of the time with flexibility to work from home up to 30%.
Moderna is pleased to provide you and your family with a comprehensive and innovative suite of benefits, including:
About Moderna
Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.
By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.
As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute and make a meaningful impact.
If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.
Moderna is a smoke-free, alcohol-free and drug-free work environment.
Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!
Moderna is proud to be an equal opportunity workplace and is an affirmative action employer.
Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. We’re focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations team at leavesandaccommodations@modernatx.com. (EEO/AAP Employer)
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