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Clinical Trial Protocol Coordinator
•Today
| Hours | Full-time, Part-time |
|---|---|
| Location | Boston, Massachusetts |
About this job
Title: Clinical Trial Protocol Coordinator
Location: Boston, MA Hybrid schedule
Start Date: ASAP
Duration: 6 Month Contract-to-Hire
Hours: Mon-Fri, 8am-4:30pm
Requirements:
BS degree in Life Sciences or related
1-2 yrs. research exp. in a Pharma, CRO, Biotech and/or Healthcare setting (Co-Op & Internship exp. would count towards this)
Willing to do some training for the right person
Excellent MS Office products exp./knowledge
Familiarity with EDC, CTMS systems and Adobe Acrobat applications “preferred” but not required.
COVID vaccine is required
Responsibilities:
Will support the dept. in the administrative day to day project activities.
Advise sites on protocol conduct, interpretation of protocols and ensures resolution of issues as applicable.
Evaluate the quality of data, issue, track and resolve queries, implement corrective action plans
Prepare presentation materials for meetings (internal/external)
Update and maintain internal databases, tracking systems and project plans with dept./trial specific information
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