Senior Clinical Research Associate
PolandFull-TimeSenior
Salary200,000 - 260,000 PLN per year
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Job Details
- Experience
- Minimum 2 years experience in independent site monitoring of all types of visits; Minimum 2 years experience in independent site monitoring in oncology
- Required Skills
- GCP
Requirements
- Extensive experience in site management
- Knowledge of clinical trial methodology and terminology
- Minimum 2 years experience in independent site monitoring of all types of visits
- Minimum 2 years experience in independent site monitoring in oncology
- Effective time management, organizational and interpersonal skills
- Problem-solving and multi-tasking skills
- Working knowledge of clinical research and clinical trial phases
- Understanding of GCP/ICH guidelines
- Knowledge of country clinical research legislation
Responsibilities
- Dedicated to a single client
- Responsible for all site management and supervisory activities in the assigned oncology studies
- Work with industry leaders and subject matter experts
- Mentor junior CRAs
- Work with world-class technology
- Perform site monitoring visits
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