Clinical Research Coordinator

Description

• Perform follow-up with study participants via telephone, e-mail, and mail.
• Maintain accurate and detailed records and files of work.
• Assist with literature reviews for proposal submissions and manuscript preparation.
• Assist in tracking study participants using MS Excel.
• Manage bookkeeping related to study budgets including ordering supplies and requesting checks for payment and participant incentives.
• Recruit and consent research participants.
• Prepare, mail, and process questionnaires and other study correspondence.
• Perform miscellaneous administrative tasks such as typing labels, copying, faxing, meeting preparation, note-taking, and transcribing audio files.
• Review, edit, clean, and enter participant data into a database.
• Conduct telephone or in-person interviews with participants, including screening for eligibility.

Requirements

• High school diploma or General Education Development (GED)
• Background in the medical field, including phlebotomy and vaccine knowledge
• Minimum of 6 months of clinical research experience

Benefits

• Employee Assistance Program
• Short and long-term disability
• Time Off/Leave (PTO, Vacation or Sick Leave)
• Medical, dental & vision
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Critical Illness, Accident, and Hospital
• Health Spending Account (HSA)
• Transportation benefits
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available

Training + Development

Interview process

Visa Sponsorship

Security clearance