Clinical Research Associate

Job Description

Join our team as a Clinical Research Associate, where you will be responsible for managing and monitoring clinical trials. This role is pivotal to our research efforts, ensuring accuracy and adherence to protocols.

Responsibilities

• Lead the management of clinical trial execution, ensuring adherence to timelines.
• Review and approve protocol amendments and ensure compliance with new regulations.
• Conduct data quality checks and perform statistical analysis on trial results.
• Create and maintain comprehensive trial documents.
• Provide mentorship to junior research staff and new hires.
• Support participant recruitment and retention strategies.
• Prepare for and facilitate regulatory inspections and audits.

Requirements

Education

• Bachelor's degree in Health Sciences or related field
• Further qualifications in Clinical Research or Project Management advantageous

Experience

• 4+ years of relevant experience in clinical settings

Technical Skills

• Data Analysis
• Project Management

Soft Skills

• Problem Solving
• Team Leadership

Certifications

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

Languages

• English: Fluent

Advantageous

• Proficiency in statistical analysis software: Experience with software such as SAS or SPSS for data analysis.
• Multi-site trial management experience: Experience coordinating trials across multiple locations.

Benefits

• Health, dental, and vision insurance
• Retirement savings plan with company match
• Paid time off and holidays
• Support for continuing education and certifications

Company Culture

• Respect: We foster an environment where all employees are respected and valued.
• Innovation and Experimentation: Our team is driven by curiosity and the pursuit of knowledge, embracing creative solutions.
• Diversity and Inclusion: We celebrate diverse perspectives and strive to create an inclusive atmosphere.