Clinical Research Coordinator

Job Description

As a Clinical Research Coordinator, you will play a critical role in the planning and execution of clinical trials. Your responsibilities will include patient recruitment, data management, and compliance oversight.

Responsibilities

• Oversee day-to-day operations of clinical trials.
• Develop and implement study protocols and procedures.
• Ensure participant safety and welfare throughout the study.
• Analyze data for accuracy and completeness.
• Draft and submit required regulatory documents.
• Coordinate with external partners and stakeholders as necessary.
• Manage the budget and resources for clinical trials.
• Conduct site visits to ensure compliance with protocols.
• Prepare for and participate in audits and inspections.
• Assist in preparing publications and presentations of trial results.

Requirements

Education

• Bachelor's degree in Nursing or related field
• Postgraduate qualification is advantageous

Experience

• 3+ years of experience in clinical trials and research

Technical Skills

• Regulatory Knowledge
• Patient Recruitment

Soft Skills

• Problem-solving
• Team Leadership

Certifications

• Good Clinical Practice (GCP) Certification

Languages

• English: Fluent

Advantageous

• Proven skills in project management: Ability to manage clinical research projects effectively.
• Familiarity with international clinical research guidelines: Knowledge of ICH-GCP and FDA regulations.

Benefits

• Health insurance and wellness programs
• Performance bonuses
• Education reimbursement for ongoing training
• Work-life balance initiatives

Company Culture

• Team Collaboration: We promote a collaborative work environment where every team member's input is valued.
• Innovation-Driven: Our focus is on innovative solutions that advance medical research and improve patient outcomes.
• Continuous Improvement: We believe in continuous learning and professional development to help our staff grow.