Clinical Research Associate

Job Description

As a Clinical Research Associate at the Medical Research Institute, you will manage the day-to-day operational aspects of clinical trials. Your responsibilities will include participant recruitment, data collection, and monitoring compliance with protocol. This is a challenging yet rewarding opportunity to contribute to significant medical advancements.

Responsibilities

• Conduct regular audits and quality checks on trial sites.
• Implement corrective actions for any non-compliance issues.
• Facilitate the communication between different teams involved in the trials.
• Assist in preparing presentations and publications based on trial data.
• Stay updated on the latest research protocols and industry regulations.
• Support the development of study materials, including informed consent documents.
• Participate in project status meetings and provide feedback on study progress.

Requirements

Education

• Master's degree in Clinical Research or Public Health is preferred

Experience

• 5+ years of experience in clinical trials management

Technical Skills

• Protocol Development
• Statistical Software

Soft Skills

• Leadership
• Problem-Solving

Certifications

• Certified Clinical Research Associate (CCRA)

Languages

• English: Fluent

Advantageous

• Experience in oncology trials: Preference for candidates with a background in oncology clinical research.
• Familiarity with data monitoring committees: Understanding of the roles and functions of clinical trial data monitoring committees.

Benefits

• Health and wellness programs
• Educational assistance for further studies
• Team-building events and activities
• Support for certifications and training

Company Culture

• Diversity and Inclusion: We value diverse backgrounds and perspectives, fostering an inclusive workplace.
• Work-Life Balance: We promote a balance between personal life and career demands.
• Community Engagement: Our commitment to community involvement and outreach is integral to our mission.