Clinical Trials Associate

Job Description

We are seeking a Clinical Trials Associate to assist in the conduct of vital clinical research. You will work closely with investigators and clinical teams, ensuring that all trial activities are executed in compliance with protocol requirements. Candidates should possess strong communication skills and a keen sense of detail, dedicated to enhancing patient safety.

Responsibilities

• Facilitate communication between investigators, clinical sites, and project managers.
• Ensure timely reporting of trial progress to stakeholders.
• Assist with data collection and analysis for trial evaluation.
• Organize and prepare for Investigator Meetings and site initiation visits.
• Evaluate and ensure proper training of site staff on trial requirements.
• Maintain high standards of confidentiality and ethics in clinical research.
• Contribute to the development of study manuals and training materials.

Requirements

Education

• Bachelor's degree in Biomedical Science or related field

Experience

• 1+ years of experience in clinical trials support

Technical Skills

• Data management

Soft Skills

• Teamwork
• Problem-solving

Certifications

• Clinical Research Coordinator (CRC) certification

Languages

• English: Fluent

Advantageous

• Experience in patient recruitment: Previous involvement in recruitment strategies for clinical trials.
• Understanding of health and safety regulations: Knowledge of protocols related to patient safety in trials.

Benefits

• Attractive salary package with bonuses
• Support for continuous education and training
• Health insurance and wellness incentives
• Generous leave policy and flexibility

Company Culture

• Empowerment: We believe in empowering our employees, providing them with the tools and support they need to succeed.
• Diversity: We are committed to diversity & inclusion in our workforce, valuing the unique perspectives of all.
• Work-Life Balance: We promote a healthy work-life balance, encouraging well-being and personal fulfilment.