Clinical Research Coordinator III

Must Haves: Must have minimum 3+ years as a Clinical Research Coordinator

Hours: 40 hours per week, Monday-Friday 8:30am-5pm, Onsite

Contract Duration: 4-6 month contract with the possibility to be hired on perm depending on performance

Benefits: Medical, Dental, Vision, time off, etc.

Role & Responsibilities:

• Pre screening, consenting, enrolling and seeing Ophthalmology patients for 18 studies. The CRC they are looking for does NOT handle data entry and regulatory on the administrative end, so they are needing someone that is highly motivated and passionate about patient interaction.

3-5 Must Have Skills/Qualifications

• 3 years experience as a CRC
• Experience on both industry funded and PI initiated trials. If they just have experience in one, it needs to be industry
• Ability to start with minimal training and know how to fully coordinate a trial (although they won't be responsible for any study start up). They will be trained on company processes and studies, but the expectation is that they know how to be autonomous

Apply Today!