Clinical Trial Protocol Coordinator

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 #m3