Regulatory Affairs Officer (Mid Level Role)
IQVIA · Lima, Peru +2 more
RegulatoryFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
IQVIA seeks a Regulatory Affairs Officer to prepare and review regulatory submission documents supporting clinical trials and marketing authorization activities across Latin America. The role involves managing regulatory projects, coordinating with internal and external clients, and maintaining compliance documentation under senior guidance.
What they're looking for
- Bachelor's degree in life sciences or related discipline
- Minimum 2 years postmarketing regulatory affairs experience
- 1 year experience tracking regulatory processes
- Fluent English (spoken, read, and written)
- Strong Microsoft Office and publishing software proficiency
- Excellent interpersonal and written communication skills
- Applicable certifications/licenses as required by local regulatory bodies
What you'll be doing
- Prepare and review regulatory documentation for chemistry, manufacturing, controls, and marketing authorization
- Identify project needs, track timelines, and manage day-to-day workload collaboratively
- Support client meetings by preparing materials and presenting regulatory information
- Participate independently in project teams with internal and external stakeholders
- Make minor process improvements and implement standard operating procedures consistently
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.