Clinical Research Coordinator II/III - Hematology (JR222446)

About the role

The Clinical Research Coordinator II/III will be responsible for managing clinical research projects within the Hematology department. This includes coordinating study activities, ensuring compliance with regulatory standards, and maintaining accurate records.

Responsibilities

• Manage day-to-day operations of clinical research studies
• Coordinate with investigators, sponsors, and regulatory agencies
• Ensure adherence to Good Clinical Practice (GCP) guidelines and regulatory requirements
• Prepare and submit required documents and reports
• Oversee the recruitment and retention of study participants
• Collaborate with other departments to ensure smooth project execution

Requirements

• Bachelor’s degree in a related field (e.g., Biomedical Sciences, Public Health)
• Minimum of 3 years of experience in clinical research
• Knowledge of GCP and regulatory requirements
• Excellent organizational and communication skills
• Ability to manage multiple tasks simultaneously

Qualifications

• Current certification in Good Clinical Practice (GCP)
• Experience with electronic data capture systems (EDC)
• Strong understanding of medical terminology and clinical research protocols

Skills

• Proficient in Microsoft Office Suite
• Strong analytical and problem-solving skills
• Excellent interpersonal and teamwork skills
• Ability to work independently and as part of a team

Benefits

• Competitive salary package
• Inclusive benefits program

Pay

Salary range: $XX,XXX - $XXXX per year

Schedule

Full-time position, Monday through Friday, 8:00 AM - 4:30 PM