Clinical Research Coordinator

Job Description

We are seeking a Clinical Research Coordinator to oversee clinical trials and ensure compliance with regulations. The successful candidate will coordinate all aspects of study implementation, including participant recruitment and data collection.

Responsibilities

• Coordinate day-to-day operations of clinical trials, ensuring timelines and milestones are met.
• Recruit, interview and screen potential study participants.
• Manage informed consent process and maintain participant confidentiality.
• Conduct site visits to monitor trial progress and assess compliance.
• Develop assessment forms and case report forms.
• Ensure that collected data is accurate, complete, and reliable.
• Assist in conducting training for new staff on research protocols.
• Prepare for and participate in audits and inspections.
• Facilitate communication between sites, research teams, and stakeholders.
• Prepare materials for investigator meetings and presentations.

Requirements

Education

• Bachelor's degree in Nursing or Public Health
• Master's degree in relevant field is an advantage

Experience

• 3+ years of experience in clinical trials or research coordination

Technical Skills

• Study Protocol Development
• Patient Engagement

Soft Skills

• Team Leadership
• Attention to Detail

Certifications

• Certified Clinical Research Coordinator (CCRC)

Languages

• English: Fluent

Advantageous

• Experience in a regulatory environment: Past experience working within a heavily regulated healthcare environment.
• Proficiency in medical writing: Ability to write scientific reports and publications based on clinical data.

Benefits

• Comprehensive health insurance coverage
• Flexible work arrangements
• Employee wellness initiatives
• Life insurance and disability coverage

Company Culture

• Learning and Development: We provide continuous learning opportunities for our staff to grow and excel.
• Diversity and Inclusion: We celebrate diversity and strive for an inclusive workplace for all.