Clinical Research Associate — Drive Site Excellence

IQVIA; Warszawa; On-site; PLN 133,000 - 280,000; Full time

Job summary

IQVIA is hiring a Clinical Research Associate to perform monitoring and site management to ensure studies are conducted per protocol and sponsor requirements. The role includes site visits, recruitment support, communication, and training across sites in Poland, with emphasis on GCP/ICH compliance and bilingual communication.

Candidates should have a Bachelor's in a scientific field or healthcare, 1 year on-site monitoring experience, and proficiency with MS Word, Excel and PowerPoint, plus

Qualifications

• Bachelor's degree in a scientific discipline or health care.
• 1 year of on-site monitoring clinical trials experience.
• Good knowledge of GCP and ICH guidelines.
• Proficient with Word, Excel and PowerPoint; comfortable with laptop and iPhone/iPad.

Responsibilities

• Perform monitoring and site management visits to ensure sites conduct the study(ies) and report data per protocol and sponsor requirements.
• Perform site selection, initiation, monitoring and close-out visits with documentation.
• Support development of a subject recruitment plan.
• Establish regular communication and administer protocol training to assigned sites.
• Evaluate quality and integrity of site practices and escalate issues as appropriate.
• Manage progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolution.

Skills

GCP/ICH knowledge

Polish & English

Communication

Teamwork

Education

Bachelor's degree in scientific discipline or health care

Tools

MS Word

Excel

PowerPoint

Laptop / iPhone / iPad

Job description

IQVIA is hiring a Clinical Research Associate to perform monitoring and site management to ensure studies are conducted per protocol and sponsor requirements. The role includes site visits, recruitment support, communication, and training across sites in Poland, with emphasis on GCP/ICH compliance and bilingual communication.

Candidates should have a Bachelor's in a scientific field or healthcare, 1 year on-site monitoring experience, and proficiency with MS Word, Excel and PowerPoint, plus