Regulatory Submissions Specialist

IQVIA Inc; Bogotá; On-site; COP 42,000,000 - 62,000,000; Full time

Job summary

IQVIA in Colombia seeks a Regulatory Affairs professional to prepare and/or review regulatory submissions for clinical trials and marketing authorization, under supervision. You will support assigned projects and collaborate with internal and external clients, applying knowledge of CMC, labeling, and publishing processes.

The role requires a Lifescience degree with 2–3 years in Regulatory Affairs, fluent English, strong communication, and proficiency with Microsoft Office and publishing tools.

Qualifications

• Bachelor's degree in lifescience or related field (concluded).
• Master's degree is a plus.
• 2–3 years relevant Regulatory Affairs experience.

Responsibilities

• Act as a Regulatory Team Member on small projects under guidance.
• Prepare/review regulatory documents for submissions.
• Collaborate with internal and external stakeholders and manage workload.

Skills

Fluent English

Interpersonal communication

Multitasking

Education

Bachelor's Degree in Lifescience or related discipline

Master's Degree in Lifescience or related discipline

Tools

Microsoft Office

Publishing applications

Job description

IQVIA in Colombia seeks a Regulatory Affairs professional to prepare and/or review regulatory submissions for clinical trials and marketing authorization, under supervision. You will support assigned projects and collaborate with internal and external clients, applying knowledge of CMC, labeling, and publishing processes.

The role requires a Lifescience degree with 2–3 years in Regulatory Affairs, fluent English, strong communication, and proficiency with Microsoft Office and publishing tools.