Scientist I

Cardinal Health

1d•$32 - $40•Remote

About The Position

The Scientist I in CMC supports regulatory activities for pre-approval, post-approval changes, and lifecycle management across client Rx and non-Rx products. Working as a consultant, this role assists in the preparation, review, and coordination of regulatory documentation, while ensuring alignment with applicable regulatory requirements and client expectations. The individual will collaborate closely with cross-functional teams and contribute to the timely delivery of high-quality regulatory submission content. What is expected of you and others at this level Applies basic concepts, principles and technical capabilities to perform routine tasks with attention to detail Works on projects of limited scope and complexity Follows established procedures to resolve readily identifiable technical problems Works under direct supervision and executes detailed instructions Develops competence by performing structured work assignments Support client projects as a consultant. Ability to work remotely from home office. Requires adaptability and responsiveness to changing project priorities.

Requirements

0-2 years of experience, open to new graduates
Bachelor's degree in related field, or equivalent work experience, preferred
Proactive, self-motivated, and able to work independently in a client-facing role.
Strong attention to detail and organizational skills.
Effective written and verbal communication skills.
Ability to manage multiple tasks and meet deadlines in a dynamic environment.
Basic proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
Working knowledge of Adobe Acrobat for document editing, formatting, and publishing.
Team-oriented mindset with the ability to collaborate across functions.

Responsibilities

Support the development, authoring, and compilation of regulatory documentation related to post-approval changes and lifecycle management activities.
Assist as an authoring strategist by organizing and maintaining submission-ready documents in accordance with regional regulatory requirements.
Collaborate with cross-functional teams (e.g., CMC, Quality) to gather and verify required information for regulatory submissions.
Ensure documentation consistency, accuracy, and compliance with internal standards and client expectations.
Track and manage document timelines and deliverables to support regulatory milestones.
Maintain clear and proactive communication with client stakeholders while operating in a contractor capacity.
Ensures an established level of billable hours per fiscal year