Clinical Research Associate

Job Description

As a Clinical Research Associate, you will play a crucial role in overseeing clinical trials from initiation to completion. Your expertise will ensure that trials run efficiently, adhering to protocols and regulatory requirements.

Responsibilities

• Oversee patient recruitment and retention efforts during clinical studies.
• Ensure that all trial documentation, including informed consent forms, are appropriately filled out.
• Track study timelines and ensure milestones are met in a timely manner.
• Facilitate communication between study sites and the sponsor.
• Assist in the development of study materials, including manuals and training guides.

Requirements

Education

• Bachelor's degree in Life Sciences, Nursing, or related field
• Advanced degree preferred

Experience

• 2+ years of experience as a Clinical Research Associate

Technical Skills

• Clinical Trial Management
• Data Analysis

Soft Skills

• Attention to Detail
• Communication Skills

Certifications

• Certified Clinical Research Coordinator (CCRC)
• Good Clinical Practice (GCP) Certification

Languages

• English: Fluent

Advantageous

• Experience with electronic data capture (EDC) systems: Familiarity with EDC systems is a plus for managing trial data effectively.
• Knowledge of statistical analysis tools: Experience with tools like SPSS or SAS for analyzing trial results.