ClinChoice /Clinical Research Associate

Overview

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.

Responsibilities

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

Requirements

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

Skills

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.