Clinical Trials Regulatory Officer - Regulatory Maintenance, Slovakia

Clinical Trials Regulatory Officer

Job Summary

The Clinical Trials Regulatory Officer prepares, reviews, and manages regulatory documentation to support clinical trial submissions in compliance with applicable regulatory requirements. The role provides regulatory support across clinical trial projects, ensuring high-quality deliverables, adherence to timelines, and effective collaboration with internal and external stakeholders.

Key Responsibilities

• Prepare and review regulatory documents for clinical trial submissions.

• Act as Clinical Trial Regulatory Manager (CTRM) on straightforward projects and support complex projects under senior guidance.

• Review scientific and regulatory documentation, conduct gap analyses, and provide recommendations to stakeholders.

• Prepare, compile, and maintain clinical trial submission dossiers in accordance with regulatory requirements.

• Provide regulatory guidance and strategic input to internal teams and external clients.

• Support local, regional, and global clinical trial submissions, including European centralized submissions where applicable.

• Ensure project deliverables are completed within scope, budget, and agreed timelines.

• Maintain high quality standards across all regulatory deliverables.

• Ensure accurate maintenance of systems, databases, tracking tools, and project documentation in line with SOPs.

• Participate in project and system audits as required.

• Perform additional duties as assigned by the Line Manager.

Qualifications & Experience

• Bachelor's degree in Life Sciences, Pharmacy, Health Sciences, or a related field.

• 2 - 3 years experience in clinical trial regulatory affairs, clinical research, or regulatory submissions.

• Knowledge of GCP, clinical trial regulations, and regulatory submission processes.

• Strong organizational, communication, and stakeholder management skills.

• Ability to manage multiple priorities while maintaining accuracy and quality.

Key Competencies

• Attention to detail

• Regulatory and scientific review skills

• Project management

• Client focus

• Quality and compliance mindset

• Collaboration and teamwork

• Effective communication skills

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is €30,800.00 - €46,200.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.