Regulatory Affairs, Specialist IV, Submission Management - Ridgefield, United States
1 week ago

Job description
, consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare.
Donec lacinia nisi nec odio ultricies imperdiet.
Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula.
Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit
, at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus.
Access all high-level positions and get the job of your dreams.
Similar jobs
This role is for a Regulatory Project Manager who will deliver project management support to the Global Regulatory Lead and Regulatory Excellence Team. The incumbent ensures project delivery in alignment with agreed upon regulatory strategy, timeline and deliverables. · Accountab ...
1 month ago
The Specialist II/III supports the US Products CMC Regulatory Affairs organization. This role provides operational support for various tasks related to regulatory submissions. · ...
1 month ago
The Content Enablement Lead is responsible to translate the asset customer experience strategy created by the therapeutic area (TA) and Sr AD into approved assets. · ...
1 month ago
As an employee of Boehringer Ingelheim you will actively contribute to the discovery development and delivery of our products to our patients and customers Our global presence provides opportunity for all employees to collaborate internationally offering visibility and opportunit ...
1 month ago
Boehringer Ingelheim is seeking an Associate Director Lead or Senior Associate Director Lead for Clinical Pharmacology. · ...
2 weeks ago
Boehringer Ingelheim is seeking a Senior Clinical Pharmacology Lead to join their team located at their Ridgefield facility. · The role will support the clinical development of new drugs and further development of approved drugs with emphasis on designing and executing Clinical P ...
1 week ago
The Director of Global Regulatory Strategy will provide strategic regulatory guidance for assigned projects. · This role involves crafting comprehensive regulatory strategies to navigate the global regulatory landscape while ensuring compliance with guidelines and regulations. · ...
2 weeks ago
We are seeking a Regulatory Affairs Specialist II/III to support our US Products CMC Regulatory Affairs organization. The ideal candidate will have experience in regulatory work and be able to maintain submissions histories for INDs/NDAs for standard drug products. · AD/BS/BA Che ...
1 month ago
The Content Enablement Lead is responsible to translate the asset customer experience strategy created by the therapeutic area (TA) and Sr AD into approved assets. · Manages multiple concurrent high visibility projects as well as works with TA and engagement teams to understand t ...
1 month ago
+We are seeking a Senior Research Fellow to support our Mental Health / Eye Health and Emerging Areas team at our Ridgefield, CT facility. · +Provides scientific input to create, organize, and implement local Research & Development programs. · Serves as a safety science lead with ...
6 days ago
The Sr Director Global Regulatory Strategy Lead plays a pivotal role in guiding assigned projects throughout product lifecycle through regulatory thought leadership and extensive experience This role will provide specific strategic and hands‑on regulatory leadership for global de ...
2 weeks ago
· The Director, Senior Clinical Program Leader assumes Clinical Development responsibilities supporting late-stage development projects, reporting to the Global Clinical Development Lead for Rheumatology. The Clinical Program Leader has a medical leadership role for a project or ...
2 days ago
This job has oversight for the design and execution of nonclinical safety programs to support the development of drug candidates from discovery to market authorization. · ...
1 week ago
Join our Stevie Award Winning Team at HUB International.<br>When you join the team at HUB International,<br>you become part of the largest privately owned global insurance broker,<br>providing a broad array of property,<br>casualty,<br>risk management,<br>life and health,<br>empl ...
1 week ago
Boehringer Ingelheim is currently seeking a talented and innovative Associate Director Lead or Senior Associate Director Lead to join our Clinical Pharmacology department located at our Ridgefield, CT facility. · ...
1 week ago
Ridgefield CT US US · ...
2 weeks ago
· Description · As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering vis ...
2 days ago
The Hospice Operations Coordinator provides essential administrative and operational support to ensure the efficient daily functioning of the Hospice department. · This role works cross-functionally to streamline processes, improve workflow efficiency, and support compliance and ...
1 month ago
The Senior Bookkeeper- Outsourced Bookkeeping Services is responsible for all aspects of bookkeeping and accounting activities for our business clients including, but not limited to, preparation of various tax forms/monthly reports. · ...
2 weeks ago
The Manager, HP Review Committee is a strategic partner and the single point of contact for the TA/brand from a Review Committee Perspective and fully understand the integrated strategic brand plans in order to efficiently and effectively manage the review, approval and productio ...
1 month ago