Browse 14 exciting jobs hiring in Submissions now. Check out companies hiring such as AbbVie, Noble People, SOKOL GxP Services in Riverside, Laredo, Madison.
Lead CMC regulatory strategy and submissions for small molecule development programs at AbbVie, managing agency interactions and cross-functional alignment to drive first-pass approvals.
Noble People seeks a detail-oriented Marketing & Sales Coordinator to translate PR wins, brand content, and cultural moments into polished sales assets and aligned internal processes.
Technical Writer needed to author and manage CMC regulatory submission content (eCTD/CTD) for a cell therapy portfolio in a hybrid, cross-functional PMO role supporting a biopharma client.
Cynet Health seeks a detail-oriented Program Support Specialist to prepare and qualify healthcare candidates for federal staffing contracts and support compliance, timeliness, and acceptance metrics.
AbbVie is hiring a Principal Research Scientist (Analytical Chemistry) to lead innovative analytical research, drive method development, mentor scientists, and contribute strategic scientific direction.
Experienced Regulatory Affairs professional needed to lead preparation and coordination of regional regulatory submissions and labeling for investigational and commercial products at Gilead in Foster City.
Experienced regulatory systems consultant needed to lead MedTech clients through enterprise deployments of Veeva RIM and related regulatory information management processes.
Skadden seeks a detail-oriented Marketing & Communications Coordinator to support proposals, awards submissions, event logistics and internal marketing operations at the firm's Los Angeles office.
Foresight Diagnostics seeks a Senior Specialist, Regulatory Affairs to lead US regulatory strategy and submissions for next-generation sequencing-based IVD products while partnering cross-functionally through development and lifecycle management.
Care Access is hiring a Regulatory Operations Specialist to manage site-level IRB and regulatory activities for U.S. clinical trials in a remote, fast-paced environment.
Gilead seeks an experienced Sr Director to lead CMC Regulatory Affairs digital transformation, driving strategy, vendor programs, and implementation of AI/ML and structured-content solutions to accelerate submissions and improve regulatory outcomes.
ORIC Pharmaceuticals seeks a Regulatory Affairs Manager to drive timely, compliant regulatory submissions and support clinical oncology programs from its San Diego office.
Support Stryker’s Regulatory Affairs team in Bloomington this summer by assisting with regulatory data collection, submission preparation, and documentation process improvements.
NBCUniversal is hiring a strategic Senior Manager, Executive Communications to drive speaking engagements, award submissions, and research-backed thought leadership that amplify Advertising & Partnerships leadership.
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