Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
PSI CRO AG

Regulatory Officer

PSI CRO AG

. Support regulatory safety reporting aspects of clinical research projects .

Posted 11/9/2026full-timeSão Paulo • BrazilMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in regulatory safety reporting within clinical research, ensuring accurate communication and documentation management. Proficient in maintaining electronic systems and tracking safety issues in compliance with regulatory standards.

Highest-signal resume keywords
Clinical Research ExperienceRegulatory Safety ReportingDocument ManagementMS Office ProficiencyCommunication Skills

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Regulatory Safety ReportingDocument ManagementClinical ResearchElectronic Systems MaintenanceTracking Systems Management
Soft Skills
Communication SkillsCollaboration SkillsMultitasking AbilityPlanning Skills
Tools & Technologies
MS Office Applications
Industry Keywords
Life SciencesSafety ReportingClinical TrialsRegulatory Compliance

About the role

Key responsibilities & impact
  • Support regulatory safety reporting aspects of clinical research projects
  • Streamline communication
  • Maintain electronic systems
  • Manage documents
  • Act as the point of contact for clinical project teams, support services and client companies on safety reporting matters
  • Coordinate accurate and time-bound reporting of safety issues to authorities
  • Handle document management, including filing, processing, and quality control
  • Update and maintain tracking systems, knowledge repositories, working files, and schedules

Requirements

What you’ll need
  • College/University degree or an equivalent combination of education, training & experience
  • Life Sciences degree is a plus
  • Prior experience in Clinical Research required, with focus on regulatory aspects of safety reporting
  • Full working proficiency in English
  • Proficiency in MS Office applications
  • Ability to plan, multitask and work in a dynamic team environment with tough deadlines
  • Communication and collaboration skills

Benefits

Comp & perks
  • Advance your career in clinical research
  • Coordinating a variety of tasks and learning new things while growing with the company