Clinical Research Coordinator

Job Description

We are seeking a detail-oriented Clinical Research Coordinator to oversee the planning and implementation of clinical trials. The ideal candidate will have a solid foundation in medical research practices, ensuring compliance with regulatory standards while coordinating with various stakeholders.

Responsibilities

• Oversee and coordinate clinical trials from initiation to close-out.
• Maintain accurate and detailed documentation of all research activities.
• Facilitate communication between investigators and study participants.
• Ensure timely completion of regulatory filings and audits.
• Implement study protocols and ensure participant safety.
• Gather and analyze clinical trial data for presentations and reports.
• Conduct site visits and monitor trial progress.

Requirements

Education

• Bachelor's degree in Healthcare, Life Sciences, or related field

Experience

• 3+ years of experience in clinical research coordination or project management

Technical Skills

• Regulatory Compliance

Soft Skills

• Problem-solving

Languages

• English: Fluent

Advantageous

• Certification in Clinical Research (e.g., ACRP, SoCRA): Valid certification demonstrating competency in clinical research principles.
• Experience with Electronic Data Capture (EDC) systems: Familiarity with various EDC systems for trial data management.

Benefits

• Competitive salary with performance bonuses
• Health and wellness benefits including medical aid
• Professional development opportunities
• Flexible working hours

Company Culture

• Team Collaboration: We encourage a collaborative atmosphere where ideas and feedback are shared openly.
• Innovation: Our team thrives on innovation, exploring new methods to enhance research outcomes.
• Inclusivity: We celebrate diversity and strive to create an inclusive environment for all.