Job Description

PharmaCores is seeking an experienced Regulatory Affairs professional to develop and deliver a pre-recorded course focused on eCTD and pharmaceutical regulatory documentation.

The instructor will provide practical, industry-focused knowledge of eCTD structure, submission documentation, regulatory requirements, and best practices.

Key Responsibilities

– Develop and structure course content covering eCTD and regulatory documentation.
– Explain eCTD structure, modules, lifecycle management, and submission processes.
– Cover relevant regulatory documentation and submission requirements.
– Provide practical examples and real-world regulatory scenarios.
– Prepare presentations and supporting course materials.
– Ensure content reflects current regulatory practices and requirements.
– Record clear and engaging video lectures.
– Collaborate with PharmaCores on course review and finalization.

Requirements

– Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, Life Sciences, or a related field.
– Professional experience in Regulatory Affairs.
– Hands-on experience with eCTD submissions and regulatory documentation.
– Strong understanding of pharmaceutical regulatory processes.
– Familiarity with major regulatory submission requirements is preferred.
– Excellent communication and presentation skills.
– Ability to explain regulatory concepts in a clear and practical manner.
– Previous teaching/training experience is a plus.