Clinical Studies Coordinator II - Translational Neuroscience

Responsibilities

• Recruitment and enrollment of subjects
• Visit scheduling
• Data collection
• Data management and quality assurance
• Regulatory duties
• Supervision of auxiliary staff
• Other relevant administrative tasks
• Tracking progress and implementing protocols with study investigators

Requirements

• Bachelor's degree with two years of experience in clinical research
• SOCRA or ACRP Certification preferred
• Must complete CITI certification for Human Subject Research
• Complete WakeOne training for research coordinators

Qualifications

• Excellent interpersonal, oral, and written communication skills
• Strong organizational skills
• EPIC/WakeOne proficiency
• Proficient in OnCore/WISER Clinical Trial Management System
• Basic computer skills
• Fosters/promotes a positive image and professional appearance
• Sensitivity to intercultural relations and confidentiality
• Knowledge of Microsoft Products

Skills

• Excellent reading comprehension
• EPIC/WakeOne proficiency
• OnCore/WISER Clinical Trial Management System proficiency
• Basic Computer skills

Benefits

• Paid Time Off programs
• Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
• Flexible Spending Accounts for eligible health care and dependent care expenses
• Family benefits such as adoption assistance and paid parental leave
• Defined contribution retirement plans with employer match and other financial wellness programs
• Education Assistance Program