Clinical Research Associate

Job Description

Seeking a detail-oriented Clinical Research Associate to oversee the implementation and management of clinical trials. The candidate will work closely with study coordinators and investigators to maintain compliance and quality standards.

Responsibilities

• Lead site initiation, monitoring, and close-out visits for clinical trials
• Perform quality assurance checks on study data and resolve discrepancies
• Coordinate communication between sites, sponsors, and clinical teams
• Assist in the review and approval of study documents and contracts

Requirements

Education

• Master’s degree in Clinical Research or related field

Experience

• 3+ years experience in a clinical research role

Technical Skills

• Clinical trial protocols
• Electronic data capture systems

Soft Skills

• Interpersonal skills
• Organizational skills

Certifications

• Certified Clinical Research Associate (CCRA)

Languages

• English: Fluent

Advantageous

• Experience leading clinical trials: Demonstrated experience in leading clinical trials from initiation to closeout.
• Published research papers: Previous publication in peer-reviewed journals is advantageous.

Benefits

• Extensive health, dental, and vision coverage
• Retirement savings plan with company contributions
• Access to continuing education programs
• Supportive and inclusive work culture

Company Culture

• Continuous Learning: We offer ongoing training and professional development opportunities for our staff.
• Diversity and Inclusion: We prioritize diversity and inclusion within our workforce.