Clinical Research Coordinator

Job Description

As a Clinical Research Coordinator, you will play a pivotal role in managing clinical trials and ensuring compliance with regulatory requirements. You will work closely with healthcare professionals and patients to facilitate research processes.

Responsibilities

• Support the research team in executing clinical studies.
• Liaise with participants to facilitate recruitment and retention.
• Conduct training for site staff on study protocols.
• Assist in data analysis and reporting findings.
• Maintain relationships with regulatory agencies.
• Ensure adherence to budgets and timelines for studies.

Requirements

Education

• Bachelor's degree in Nursing or Public Health

Experience

• 3+ years in a clinical research setting

Technical Skills

• Regulatory Compliance
• Study Design

Soft Skills

• Problem-solving
• Team Leadership

Certifications

• Clinical Research Associate (CRA) Certification

Languages

• English: Fluent

Advantageous

• Experience with statistical analysis software: Hands-on experience with software like SPSS or SAS for analyzing clinical data.
• Project management experience: Background in managing research projects and coordinating timelines.

Benefits

• Health and wellness programs
• Paid time off for volunteer activities
• Annual bonus based on performance
• Support for ongoing education and training

Company Culture

• Continuous Improvement: We support the ongoing development of our team through training and professional growth opportunities.
• Diversity and Inclusion: We celebrate diversity and are committed to creating an inclusive workplace for all.
• Community Engagement: We actively engage with the community to improve health outcomes and raise awareness about clinical research.