Clinical Research Coordinator II - ERP International

ERP International, LLC (www.erpinternational.com) is currently seeking a Clinical Research Coordinator II for a full-time position supporting the Walter Reed Army Institute of Research (WRAIR) at Silver Spring, MD.  Please apply online to learn more about this great opportunity!

We appreciate your interest in becoming part of our team. Although this requisition does not apply to a specific immediate opening , we value proactive candidates like yourself who are looking to build a meaningful career with ERP International. We will keep your application on file and contact you when suitable opportunities arise. (Applying for the future openings posting does not guarantee employment)

Be the Best!  Join our team of exceptional clinical talent across the nation.  Come discover the immense pride and job satisfaction ERP Employees experience in providing care for our Military Members, their Families and Retired Military Veterans!  ERP International is honored to have been named one of The Washington Post’s 2024 Top Workplaces!

ERP Offers Employees:

* Competitive Salaries & Benefits!
* Health Advocate & Concierge Services!
* Unlimited Job- Related Training & Development!

* Employee Recognition & Incentive Programs!

* Employee Appreciation & Company Sponsored Events!
* Opportunity to work with leading edge technology!

* Community Outreach & Charity Work!

About ERP International, LLC: ERP is a nationally respected provider of health, science, and technology solutions supporting clients in the government and commercial sectors. We provide comprehensive enterprise information technology, strategic sourcing, and management solutions to DoD and federal civilian agencies in 40 states. Founded in 2006, ERP is headquartered in Laurel, MD and maintains satellite offices in Montgomery, AL and San Antonio, TX - plus project locations nationwide. ERP is an Equal Opportunity Employer - Disability and Veteran.

Participates in the design and monitoring of clinical trials. Analyzes and evaluates clinical data gathered during research. Ensures compliance with protocol and overall clinical objectives. Perform clinical research coordination as directed by the Internal Review Board (IRB), providing protocol coordination, assistance with proposal writing projects, and assistance with progress and technical reports.Organize and prioritize all activities associated with conducting laboratory and field based human use protocols. Maintain compliance with specific protocol, SOPs, regulations, and guidelines.

Requires a BS, RN, or BSN degree or equivalent and a minimum of 5 years of experience in the field or in a related area. Knowledge of FDA regulatory requirements is required. Familiar with a variety of the field's concepts, practices, and procedures. Relies on experience and judgment to plan and accomplish goals. Performs a variety of complicated tasks. A wide degree of creativity and latitude is expected.