Clinical Research Coordinator

Job Description

We are looking for a Clinical Research Coordinator to oversee and coordinate clinical trials and studies. The ideal candidate should have a strong background in medical research, excellent organizational skills, and the ability to work collaboratively with healthcare professionals and researchers.

Responsibilities

• Manage study budgets, timelines, and resources efficiently.
• Coordinate meetings with study teams and stakeholders.
• Analyze data trends and prepare reports for stakeholders.
• Work with IRB and regulatory agencies for approvals.
• Train new staff on clinical trial protocols and procedures.

Requirements

Education

• Bachelor's degree in Nursing or Health Sciences
• Master's degree in Public Health or a relevant field is preferred

Experience

• 3+ years of experience in clinical trials or research coordination

Technical Skills

• Study Protocol Development
• Statistical Analysis Software (SAS)
• Ethics and Compliance Oversight

Soft Skills

• Interpersonal Skills
• Organizational Skills

Certifications

• Certified Clinical Research Associate (CCRA)
• Clinical Research Ethics Certification

Languages

• English: Fluent

Advantageous

• Proficiency in medical terminology: Strong understanding of medical terminology used in research settings.
• Previous experience in patient advocacy: Knowledgeable in promoting patient rights and ethical considerations.

Benefits

• Comprehensive health coverage including mental health support
• Annual professional development budget
• Employee wellness initiatives
• Work-life balance programs

Company Culture

• Empowerment: We empower our team members to take initiative and lead projects.
• Diversity and Inclusion: We celebrate diversity and create an inclusive environment for all employees.