FULL TIME|Not specified, Not specified|Опубликовано 2/25/2026
ClinChoice /Clinical Research Associate
Описание
ClinChoice is seeking a Clinical Research Associate (CRA) to support the execution of clinical trials in compliance with regulatory requirements and Good Clinical Practice (GCP). The role involves monitoring study sites, ensuring data integrity, and coordinating with investigators and sponsors to ensure successful study delivery.
Обязанности
- Monitor clinical trial sites and ensure protocol compliance
- Review and verify clinical data accuracy
- Ensure adherence to GCP and regulatory requirements
- Communicate with investigators and study coordinators
- Prepare monitoring reports and documentation
- Support study start-up and close-out activities
- Identify and resolve study-related issues
Требования
- Experience in clinical research or clinical trial monitoring
- Knowledge of GCP and regulatory guidelines
- Strong documentation and reporting skills
- Excellent communication and organizational abilities
- Ability to travel if required
- Background in life sciences, pharmacy, or medicine preferred
- Fluent English communication skills
Навыки
Clinical ResearchGCP ComplianceRegulatory AffairsTrial MonitoringData VerificationHealthcare ResearchDocumentationCommunication SkillsClinical Operations
ClinChoice
ClinChoice is a global full-service Contract Research Organization (CRO) providing clinical development, regulatory, and post-marketing support services to pharmaceutical, biotechnology, and medical device companies. Founded in 1995, the company supports the full product lifecycle—from early-phase clinical trials to commercialization and pharmacovigilance. ClinChoice offers services including clinical operations, data management, biostatistics, regulatory affairs, quality assurance, and medical writing. The company operates internationally and is recognized for delivering high-quality, compliant, and efficient solutions within highly regulated healthcare environments.