As a Digital Regulatory Project Manager, you will spearhead the execution of digital for regulatory projects in support of Moderna's Digital roadmap. In this role, you will collaborate with various stakeholders and contributors from regulatory operations, medical writing, and regulatory strategy to advance digital projects for regulatory.
This role will report into the Principal Project Manager, Clinical Informatics.
Here’s What You Will Do:
Act as the project manager for Moderna’s structured content authoring (SCA) platform deployment:
Identify project deliverables such as content model and taxonomy, components artifacts
Monitor and manage project risks as needed
Facilitate governance meetings and status updates
Coordinate activities and timelines with external vendors and Digital Centers of Excellence (Cloud operations, cyber security)
Lead Artificial Intelligence (AI) projects in for regulatory in collaboration with our Data Science and AI team:
Collect and organize AI project artifacts
Work with AI team to scope and assign the relevant project team members
Lead Integration projects which entail a solid understanding of different technical workstreams and dependencies and incorporate them in overall project timelines
Establish and manage project timelines and project deliverable
Work collaboratively across the organization to gain alignment on project goals and deliverables
Engage with Computer Systems Validation team to support validation activities (as needed)
Report on projects progress and status
Here’s What You Will Bring to the Table:
7+ years' experience in digital project management (GxP experience a plus)
Proven experience with Regulatory processes and platforms (Veeva preferred).
Tangible record of accomplishment in using Agile approaches in a regulated environment
As a technologist, you know your craft and you are fluent in the digital world. You have first-hand knowledge of SaaS (Software as a Service) technology in a GxP environment and practical understanding of data integrity requirements for systems used in the conduct of clinical trials.
You have a working knowledge of regulatory business processes in a drug development context
You work independently yet engage proactively with team members, colleagues, and stakeholders to get alignment and drive projects forward.
You do not hesitate to dive in and work alongside your team. You can effectively manage conflicting priorities in a fast-paced environment, and you can navigate ambiguity and lead a team effectively
You put team before tasks by collaborating actively with all team members and supporting them.
Bachelor's degree in Computer Science, Biotechnology or equivalent required.
Job Types: Temporary, Contract
Pay: $55.00 - $65.00 per hour
Compensation package:
Experience level:
Schedule:
Ability to commute/relocate:
- Cambridge, MA: Reliably commute or planning to relocate before starting work (Required)
Work Location: In person