Sponsor-Focused Clinical Trial Submissions Coordinator

IQVIA LLC; Warszawa; On-site; PLN 106,000 - 374,000; Full time

Job summary

IQVIA LLC is seeking a regulatory affairs professional with 3–5 years of experience in CTR submissions. The role requires strong knowledge of GCP, ICH guidelines, and applicable regulatory requirements to ensure compliant clinical trial submissions within a fast-paced environment.

Candidates will coordinate multiple activities, manage timelines, and contribute to the integrity of the regulatory process. The company emphasizes ethical hiring and full transparency in the recruitment process and

Qualifications

• 3–5 years of experience preparing and managing CTR submissions.
• Strong knowledge of GCP, ICH guidelines, and applicable regulatory requirements.
• Experience in regulatory affairs and clinical trial submissions.
• Proven project management skills to coordinate multiple activities and meet deadlines.

Skills

CTR submissions

GCP

ICH guidelines

regulatory affairs

clinical trial submissions

project management

Job description

IQVIA LLC is seeking a regulatory affairs professional with 3–5 years of experience in CTR submissions. The role requires strong knowledge of GCP, ICH guidelines, and applicable regulatory requirements to ensure compliant clinical trial submissions within a fast-paced environment.

Candidates will coordinate multiple activities, manage timelines, and contribute to the integrity of the regulatory process. The company emphasizes ethical hiring and full transparency in the recruitment process and