Clinical Research Associate

Job Description

As a Clinical Research Associate, you will take charge of coordinating all aspects of clinical trials, from initial planning through execution. You will collaborate with healthcare professionals to ensure timelines are met and data is gathered accurately, contributing to significant advancements in medical research.

Responsibilities

• Conduct on-site monitoring visits to ensure compliance.
• Prepare and deliver presentations on trial progress to stakeholders.
• Collaborate in the development of educational materials.
• Manage regulatory documents and ensure submission deadlines are met.
• Coordinate responses to audit findings and implement corrective actions.
• Foster positive relationships with investigators and research staff.
• Ensure submission of timely and accurate data to stakeholders.
• Remain updated on relevant clinical research regulations and trends.

Requirements

Education

• Bachelor's degree in Medicine, Pharmacy, or related field
• Master's degree preferred

Experience

• 4-6 years' experience in clinical research, with specific experience in a monitoring role preferred.

Technical Skills

• Clinical Research Methodologies
• Statistical Analysis Software

Soft Skills

• Attention to Detail
• Adaptability

Certifications

• Certified Clinical Research Coordinator (CCRC)
• ISO 14155 Certification

Languages

• English: Fluent

Advantageous

• Familiarity with international clinical trial regulations: Understanding of regulations governing clinical trials globally.
• Knowledge of pharmacovigilance practices: Experience in monitoring and reporting adverse drug reactions.

Benefits

• Attractive salary and bonuses based on performance
• Full healthcare coverage including dental and vision
• Work-life balance emphasis with generous leave entitlements
• Funding for training and professional certificates
• Remote working options available

Company Culture

• Community Health Focus: Our research aligns with community health needs and seeks to improve patient outcomes.
• Continuous Improvement: We are committed to continuous improvement and transparency in our research processes.
• Inclusivity: We aim to create a diverse and inclusive workplace where every voice is valued.