Senior Clinical Research Associate, Sponsor dedicated in Poland

Are you interested in collaborating with leading pharma companies to help patients all around the world? When you join IQVIA as a sponsor‑dedicated Senior CRA in Poland, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our clients. Whether you’re just starting out or looking to deepen your expertise, this role promises intentional career growth and professional development.

Responsibilities

• Perform site selection, initiation, monitoring, and close‑out visits.
• Support development of a subject recruitment plan.
• Evaluate the quality and integrity of site practices in accordance with regulatory requirements (GCP, ICH).
• Manage progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution.
• Collaborate with experts at study sites and client representatives.
• Participate in remote monitoring, study start‑up processes, or therapeutic‑area specialization as required by the client model.

Qualifications

• University degree in life science or a related scientific discipline, or apprenticeship in health care.
• Minimum three years of on‑site monitoring experience, or an equivalent combination of education, training, and experience.
• Strong experience in monitoring clinical trials.
• Knowledge of applicable regulatory requirements (GCP, ICH).
• Strong written and verbal communication skills, attention to detail, and ability to work in a fast‑paced environment.
• Good command of Polish and English language.
• Flexibility to travel.

Benefits

• Resources to promote your career growth.
• Leaders that support flexible work schedules.
• Programs to help you build therapeutic knowledge.
• Dynamic work environments that expose you to new experiences.
• Home‑office, company car, and more.

The potential base pay range for this role, when annualized, is 171,900.00 zł – 375,700.00 zł. The actual base pay offered may vary based on qualifications, location, and/or schedule. Incentive plans, bonuses, and other compensation may also be offered, along with a range of health and welfare benefits.

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.