INOVA CmbH - Falls Church, VA

posted 3 months ago

Full-time - Entry Level
Falls Church, VA
10,001+ employees
Furniture and Related Product Manufacturing

About the position

The Clinical Research Coordinator I plays a crucial role in implementing research studies and ensuring the protection of research subjects within Inova Health System. This position encompasses a wide range of responsibilities, starting from site selection to the closure of studies. The coordinator is tasked with coordinating the financial aspects of study implementation and management, which includes assessing protocol feasibility and overseeing the financial management throughout the study lifecycle. The role requires the development of a foundational understanding of study coordination, allowing the coordinator to perform various tasks under direct supervision. The Clinical Research Coordinator I will participate in diverse clinical studies, which may involve investigational products, different study phases, and various therapeutic areas and indications. This position is essential for maintaining compliance with Good Clinical Practice (GCP) and ensuring that all study activities are conducted in accordance with regulatory requirements. The coordinator will also be responsible for explaining key protocol elements, subject safety measures, and the investigational product development process to ensure that all team members and study participants are well-informed and protected throughout the research process. Inova Health System is committed to providing a supportive environment for its employees, emphasizing professional development and continuous improvement in healthcare delivery. The organization values its team members and strives to create a compassionate future for healthcare, making this position integral to achieving those goals.

Responsibilities

  • Identifies and explains key protocol elements and performs study tasks under direct supervision.
  • Explains basic elements of subject safety including the reasoning behind the required use of an Institutional Review Board/Independent Ethics Committee, study activity documentation, and event reporting requirements.
  • Demonstrates subject protection under direct supervision.
  • Explains the investigational products development process and identifies key regulations to control these processes.
  • Explains and performs study operational activities in compliance with Good Clinical Practice (GCP), and non-GCP related study management activities.
  • Explains how to document data according to ALCOA-C (Attributable, Legible, Contemporaneous, Original, Accurate and Complete) principles.
  • Other duties as assigned.

Requirements

  • Minimum Education: Associate degree (or relevant experience in lieu of degree)
  • Years of Experience: Two years patient care experience or 1-year clinical research experience with a bachelor's degree.

Benefits

  • Health, Vision, and Dental Coverage
  • Life Insurance, Short/Long Term Disability
  • 4 weeks PAID PARENTAL LEAVE
  • Retirement: Inova matches dollar for dollar the first 5% of your eligible pay that you contribute to the plan
  • Competitive salary: Pay based on experience
  • Amazing Paid Time Off: Accrue PTO hours on your very first day of work
  • Supplemental Plans: Including Auto/Home Insurance discounts, Pet Insurance, Identity Theft Protection
  • Educational Assistance of up to $5,250/year
  • Student Loan Refinancing
  • Adoption Assistance
  • Child Care Centers
  • Scholarship Program
  • Free Parking
  • Exclusive savings opportunities to in-store events, theme parks, discounts, movie tickets and local offerings.
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