Clinical Research Coordinator

Job Description

We are seeking a Clinical Research Coordinator to manage and oversee study protocols for a variety of clinical trials. The ideal candidate will have strong organizational skills, excellent attention to detail, and a passion for advancing medical research.

Responsibilities

• Oversee the implementation of study protocols and SOPs.
• Ensure timely enrollment of study participants.
• Conduct regular audits of trial documentation.
• Facilitate communication between the research team and external stakeholders.
• Manage data entry and database management for study records.
• Assist in the preparation of publications and presentations related to research findings.

Requirements

Education

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

Experience

• 2+ years of clinical research experience, preferably in a coordinator role

Technical Skills

• Data Management
• Patient Interaction

Soft Skills

• Organizational Skills
• Team Leadership

Certifications

• Certified Clinical Research Associate (CCRA)
• Basic Life Support (BLS) Certification

Languages

• English: Fluent

Advantageous

• Experience in patient recruitment strategies: Skilled in utilizing various techniques to enhance patient enrollment in studies.
• Familiarity with project management tools: Experience with tools such as Trello or Asana for managing trial timelines.

Benefits

• Comprehensive health coverage including dental and vision
• Flexible spending accounts and 401(k) with match
• Generous PTO policy and wellness programs
• Opportunities for conferences and training

Company Culture

• Diversity and Inclusion: We embrace a diverse workforce and value varied perspectives.
• Supportive Environment: We provide a supportive atmosphere for both professional growth and personal wellbeing.
• Continuous Learning: We invest in the ongoing education and development of our team members.