Clinical Research Coordinator

Overview

Role
:
Clinical Research Coordinator - 6 month contract. Relocation candidates will NOT be considered for this position. Role is 100% onsite, there is no opportunity for hybrid or remote work at this time.

Therapeutic Area
:
Infectious Disease

Employment Type
:
Position is a contract, project based support role - current contract duration is estimated to be 6 months, possibility for extension depending on project needs

• 18 hours a week - The site is open to the CRC working 3, 6 hours days during the week. Their hours are from 8-5 Mon-Fri and they are flexible on which days/hours the CRC works within this time frame.
• MUST work M-F during daytime business hours - NO evenings/weekends, open to reviewing candidates  preferred schedules

Looking for an individual to provide data entry and verification support for two cardiology studies. Both trials have data backlogs that will require clean-up, and PI has relayed that other back-end data support (such as organizing patient binders and tracking down source documents) will be necessary too.

EDC (Electronic Data Capture) data entry involves accurately transcribing clinical trial data from source documents into the EDC system in a timely manner. Site staff are responsible for ensuring that all entered data is complete, consistent, and in compliance with the study protocol. Query resolution includes reviewing and responding to data queries raised by monitors or data managers, which may involve clarifying discrepancies, updating information, or providing additional documentation.

• Candidate must exhibit a high level of organization, professionalism, and initiative
• Minimum 1 year experience with clinical trial coordination required
• Minimum 1 year experience with EDC data entry and query resolution required
• Experience / knowledge related to oncology or Medical Devices preferred