We are seeking a Clinical Research Coordinator to oversee clinical trials, ensuring compliance with protocols and regulations. The ideal candidate will possess strong organizational skills and a background in medical research.
Responsibilities
Lead the coordination of clinical trials from start to finish.
Ensure all activities comply with GCP guidelines.
Work closely with the research team to develop study timelines.
Facilitate training for site staff on protocols.
Assess and manage project budgets and timelines.
Assist in conducting site visits and audits.
Requirements
Education
Bachelor's degree in Nursing or Medical Sciences
Master's degree in Research Management is advantageous
Experience
3+ years of clinical research experience preferred
Technical Skills
Data Analysis
Project Management
Soft Skills
Team Leadership
Adaptability
Certifications
Health Research Ethics Certification
Certified Clinical Research Associate (CCRA)
Languages
English: Fluent
Advantageous
Skills in patient recruitment strategies: Experience in designing effective strategies for recruiting study participants.
Proficient in statistical software: Experience using statistical analysis software for data interpretation.
Benefits
Comprehensive health benefits package
Annual leave and paid time off
Access to professional development resources
Employee wellness programs
Company Culture
Professional Development: We prioritize the growth of our employees through training and mentorship.
Community Engagement: We encourage employee participation in community service and outreach programs.
Work-Life Balance: We value a healthy work-life balance and offer flexible scheduling.