Clinical Research Associate II - Remote

Please apply online using a laptop or desktop computer.

POSITION SUMMARY:

This position supports the CIBMTR CRO Services team supporting and leading the management of one or more multi-center clinical research studies.

This position independently performs site monitoring visits to complete source document verification and assess site compliance.

Additionally, this position is responsible for coordinating and providing support for all aspects of the study including protocol and site management, providing training to junior team members, and demonstrates comprehensive knowledge of the monitoring functions.

This is a remote position (US) but candidates must be located within 30-60 minutes of a major airport.

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ACCOUNTABILITIES:

Monitoring:


* Independently perform full-scope remote and on-site monitoring visits involving source document verification, review of essential regulatory documents, and assessing site performance.


* Ensure compliance with clinical trial protocols based on regulations, ICH GCP guidelines, and NMDP standard operations procedures.


* Identify and communicate site findings with site study personnel and the study team.


* Perform query management activities and generate study and site status reports.


* Independently analyze trends in identified issues and author visit reports and letters.

Ensures documentation and resolution of identified issues and implementation of corrective and preventative action.


* May serve as Lead CRA on studies with multiple assigned CRAs, including developing and monitoring of study metrics, overseeing clinical monitoring plan compliance and escalating study risk, with supervision.

Site Management:


* Oversee and manage operational aspects of clinical trial sites in conjunction with project teams.


* Assists with site activation and ensures study start-up and enrollment goals are met.


* Collect and review essential documents for investigational sites, including maintenance of electronic Trial Master File.


* Serves as primary liaison for site management issues for assigned studies, escalating to the clinical project manager as required.


* Utilizes effective and proactive communication, relationship building, and issue management to develop and maintain good working relationships with Investigators and site staff.


* Provide support to Investigators, Study Coordinators, and other appropriate staff personnel regarding study workflow, overcoming obstacles, and general questions regarding study conduct.

Centralized Monitoring:


* Leads and trains others in reviewing study site data and data reports to ensure timely and accurate submission and compliance with the study protocol.

Other Duties as Required for Clinical Operations:


* Performs all duties in compliance with standard operating procedures, regulations outlined in the Code of Federal Regulations (CFR), ICH GCP gu...