Clinical Research Associate

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.

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

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

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.