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Part-Time Clinical Research Coordinator
4 months ago
Part-Time Study Coordinator (20 hours per week)
* This is a short term contract position and requires clinical research experience for this role*
Job Description:
Looking to hire an onsite part time individual with clinical research experience to act as a consultant to support an ongoing Ophthalmology clinical trial. This Study Coordinator must be experienced in being able to work independently. You will act as one of the main Study Coordinator's for this study. Please note, as the position and study progress, additional job duties will likely be added that are not listed in this description. A candidate must help the site and study wherever needed depending on the specific assignment.
Responsibilities:
* Ongoing Chart review
* Phone screening
* Patient recruitment
* Collection of study data and entering into EDC
* Resolving queries
* E-diary compliance
* Study start up
* IRB approval
* Monitor visits
* Assist with timely reporting of AEs/SAEs
* Retention support
* Media referral processing
* Creating source documents
* Medical record retrieval
* Scheduling appointments
* Appointment reminders
* Any study efforts deemed necessary by the site
Requirements:
* Minimum of two years in a Clinical Research Coordinator or Study Coordinator role
* Ophthalmology experience required
* Experience with MyPatient EMR preferred
* Experience with electronic medical records (EMR)
* Experience with electronic data capture (EDC) systems
* Wiling to obtain Good Clinical Practices (GCP) certified
Additional Details:
Location: Newark, NJ
Duration: Open ended contract (3-6 months with possible extension)
Schedule: Onsite 20 hours/week - during normal business hours
Pay range: $25-35 per hour
Start date: ASAP
This position will remain at part time hours, there is no potential for full time hours
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