Clinical Research Coordinator

Job Description

We are seeking a detail-oriented Clinical Research Coordinator to join our team in Des Moines. The ideal candidate will coordinate clinical studies, ensuring compliance with regulatory and ethical standards while managing patient interactions and documentation.

Responsibilities

• Lead recruitment efforts and assist participants throughout the trial phase.
• Ensure all trial operations align with ethical standards and compliance guidelines.
• Analyze data and assist in drafting research publications and presentations.
• Engage with community partners to foster relationships that aid in recruitment efforts.
• Assist in the development of new protocols for upcoming studies.
• Help establish and enforce budgetary constraints and project timelines.

Requirements

Education

• Bachelor’s degree in a related field
• Master’s degree preferred

Experience

• 3+ years of experience in a clinical research setting

Technical Skills

• Regulatory Compliance
• Project Management Software

Soft Skills

• Problem-Solving
• Team Leadership

Certifications

• Clinical Research Associate (CRA) Certification
• Certified Clinical Research Coordinator (CCRC)

Languages

• English: Fluent

Advantageous

• Familiarity with statistical analysis software: Experience with software such as SPSS or SAS for data analysis.
• Bilingual in Spanish: Ability to communicate effectively with Spanish-speaking participants.

Benefits

• Comprehensive health benefits including dental and vision
• Generous vacation and sick leave policies
• 401(k) retirement plan with matching contributions
• Ongoing training and development programs

Company Culture

• Diversity: We value diversity and strive to create an inclusive environment where all employees feel welcomed and valued.
• Growth: We are committed to investing in our employees' professional growth and development.