Clinical Research Coordinator

Job Description

The Oncology Clinical Research Coordinator will be integral to our clinical research efforts. You will orchestrate clinical trials, ensuring that all protocols are followed, and coordinate patient recruitment and retention strategies.

Responsibilities

• Assist in the design and implementation of clinical trials in oncology.
• Coordinate trial activities including participant recruitment and adverse event reporting.
• Develop and maintain study documentation, including protocols and consent forms.
• Liaise with external partners and ensure compliance with relevant guidelines.
• Conduct site initiation, monitoring, and close-out visits.
• Provide training and support to study staff and investigators.
• Contribute to the development of publications and presentations.
• Participate in team meetings and contribute to ongoing process improvement.

Requirements

Education

• Bachelor's degree in a related field

Experience

• 3+ years in clinical research coordination, with experience in oncology preferred.

Technical Skills

• Experience with electronic medical records systems
• Statistical analysis software (e.g. SAS, R)

Soft Skills

• Attention to detail
• Problem-solving

Certifications

• Master's degree in Healthcare or Clinical Research (advantageous)

Languages

• English: Fluent

Advantageous

• Familiarity with clinical trial phases II, III, and IV: Expertise in managing and understanding different trial phases.
• Experience with international clinical studies: Knowledge of managing global trials, following international regulations.

Benefits

• Comprehensive health insurance coverage.
• Employee assistance programs.
• Paid time off for volunteer work.
• Career advancement support.

Company Culture

• Continuous Learning: We provide ongoing training and professional development opportunities to grow your skills.
• Work-Life Balance: We understand the importance of balance and support flexible working conditions.