(Contract) Document Associate

The Role:

This role is an exciting opportunity to be an integral part of the talent engine fueling a high growth organization that is radically changing the biotech industry. Reporting to the Senior Director, Regulatory Operations, the Document Associate, Regulatory Operations will be responsible for assisting with document formatting, publishing, quality control, and interactions with third party vendor(s) to ensure compilation of high-quality electronic submissions.

Here's What You'll Do:

• Compile and submit eCTD, paper, or PDF submissions using publishing systems.
• QC and format documents to ensure they meet submission-ready standards.
• Ensure that documents are filed and archived properly in accordance with Moderna requirements.
• Interact with third party vendor to ensure eCTD submissions are submitted on time and are free of validation errors.
• Assist with the update of publishing processes and SOPs.
• Assist in training and ensuring awareness to regulatory and cross functional colleagues on the use of Regulatory Systems (e.g. Document Management, eCTD Review tools) and related processes.

Here's What You'll Bring to the Table:

• Bachelor's degree with relevant experience, including electronic document management systems, global regulatory systems, other experience directly related to Regulatory Operations (1-2 years minimum).
• Experience publishing eCTD, and other submission types, for submission to the FDA, and EMA, and other health authorities preferred.
• Strong organizational skills.
• Critical thinking/problem-solving skills.
• Ability to operate in a fast-paced environment and manage multiple activities, priorities and deadlines
• Strong interpersonal skills to communicate and collaborate with multiple groups.
• Proficiency with computer programs such as MS Office, Power Point, and Adobe Acrobat.

Why join Moderna

At Moderna, we believe messenger RNA, or mRNA, is the "software of life." Every cell in the body uses mRNA to provide real-time instructions to make the proteins necessary to drive all aspects of biology, including in human health and disease. Given its essential role, we believe mRNA could be used to create a new category of medicines with significant potential to improve the lives of patients.

Headquartered in Cambridge, Mass., Moderna currently has strategic alliances for development programs with AstraZeneca, Plc. and Merck, Inc., as well as the Defense Advanced Research Projects Agency (DARPA), an agency of the U.S. Department of Defense; and the Biomedical Advanced Research and Development Authority (BARDA), a division of the Office of the Assistant Secretary for Preparedness and Response (ASPR) within the U.S. Department of Health and Human Services (HHS). Moderna has been ranked in the top ten of Science's list of top biopharma industry employers for the past four years. To learn more, visit www.modernatx.com .

Our Mission:
Deliver on the promise of mRNA science to create a new generation of transformative medicines for patients.

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Moderna is a smoke-free, alcohol-free and drug-free work environment.

Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. Moderna will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.