Clinical Research Coordinator (Warsaw, Poland, FT)
- Warszawa, mazowieckie
- Stała
- Pełny etat
- Facilitating the coordination and execution of clinical research studies, including participant recruitment, enrollment, and follow-up activities.
- Collaborating with principal investigators, study sponsors, and regulatory authorities to ensure compliance with study protocols, regulatory requirements, and ethical standards.
- Collecting and maintaining accurate and complete clinical trial data, including documentation of adverse events, protocol deviations, and study outcomes.
- Managing study-related documentation, including informed consent forms, case report forms, and regulatory submissions.
- Providing support and guidance to study participants, including education, counseling, and assistance with study-related procedures.
- Bachelor's degree in a relevant scientific discipline or healthcare-related field.
- Previous experience working in clinical research or healthcare settings preferred.
- Knowledge of clinical research regulations, including FDA/EMA regulations, ICH-GCP guidelines, and HIPAA requirements.
- Strong organizational, communication, and interpersonal skills, with the ability to work effectively in a team environment.
- Detail-oriented with the ability to manage multiple tasks and priorities simultaneously.