Clinical Research Coordinator

Job Description

As a Clinical Research Coordinator, you'll play a vital role in managing clinical trials and ensuring compliance with regulatory standards. Ideal candidates will have experience in medical research and be passionate about contributing to advancements in healthcare.

Responsibilities

• Implement and monitor clinical protocols, ensuring compliance throughout the trial.
• Act as the primary contact for study participants and address their concerns.
• Assist in the preparation of grant applications and study reports.
• Analyze trial data and prepare presentations for stakeholders.
• Participate in regular team meetings to discuss trial progress and challenges.
• Ensure proper storage and handling of clinical data and biological samples.

Requirements

Education

• Bachelor's degree in Nursing or Pharmacy
• Master's degree in Public Health is preferred

Experience

• 5+ years of experience in clinical research or project management

Technical Skills

• Regulatory Compliance
• Project Management

Soft Skills

• Leadership
• Adaptability

Certifications

• Certified Clinical Research Associate (CCRA)
• ISO 14155 Compliance Training

Languages

• English: Fluent

Advantageous

• Experience with GCP inspections: Familiarity with preparing for and responding to regulatory inspections.
• Strong networking skills with healthcare providers: Ability to establish and maintain relationships with stakeholders.

Benefits

• Comprehensive medical, dental, and vision coverage
• Retirement savings plan with company contributions
• Continuous learning and development programs
• Supportive work environment promoting career advancement

Company Culture

• Diversity and Inclusion: We value diversity and strive to create an inclusive environment for all employees.
• Continuous Improvement: We are committed to continuous improvement and value feedback to enhance our work.
• Community Engagement: We actively engage with our community to promote health and well-being.