What are the responsibilities and job description for the Clinical Research Coordinator III - 238113 position at Medix™?
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
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Salary : $28 - $38
