Senior Research Associate - Emergency Medicine Atrium Health

  • Atrium Health
  • Charlotte, North Carolina
  • Full Time

Grant-Funded

Atrium Health is seeking a highly motivated and enthusiastic Senior Research Associate to join our dynamic Clinical Research team! This is an exceptional opportunity for a recent graduate with a Bachelor's degree to launch their career in a leading healthcare system. We are looking for an individual eager to contribute to cutting-edge research and make a meaningful impact on patient care.

About Atrium Health: Atrium Health is a nationally recognized leader in healthcare, committed to providing the highest quality patient care, conducting innovative research, and educating the next generation of healthcare professionals. Our clinical research endeavors span a wide range of therapeutic areas, contributing to medical advancements and improving health outcomes for our communities.

Position Summary: The Senior Research Associate will play a vital role in the execution and coordination of clinical research studies. Under the guidance of experienced investigators and research managers, this position will be responsible for a variety of tasks that support the successful conduct of clinical trials from start-up to close-out. This is an ideal role for a new graduate who is eager to learn, grow, and contribute to a fast-paced research environment.

Will be working with patients and providers in the Emergency Department to screen and enroll in ongoing clinical trials. Collects and processes blood samples in the research laboratory and performs review of the medical records and completes data entry.

Collects, enters and analyzes research data. Provides reports using computerized databases and information systems. Prepares reports from requests from the director, faculty, study sponsor, and outside collaborators. Designs, implements, and evaluates request using databases as information source.

Responsibilities:

  • Assist with the preparation and submission of regulatory documents to Institutional Review Boards (IRBs) and other regulatory bodies.
  • Support the recruitment, screening, and enrollment of study participants in accordance with study protocols and regulatory guidelines.
  • Coordinate and schedule participant visits, ensuring all study procedures are completed accurately and on time.
  • Collect, record, and maintain study data in case report forms (CRFs) and electronic data capture (EDC) systems, ensuring data integrity and quality.
  • Assist with the management of study specimens, including collection, processing, and shipment, adhering to proper laboratory procedures and protocols.
  • Maintain accurate and organized study files, including regulatory binders, participant charts, and source documentation.
  • Monitor and report adverse events and protocol deviations in a timely manner.
  • Participate in monitoring visits and audits, providing necessary documentation and support.
  • Collaborate effectively with investigators, research nurses, study coordinators, and other team members.
  • Stay up-to-date with current Good Clinical Practice (GCP) guidelines, federal regulations, and institutional policies.
  • Assist with other research-related duties as assigned.

Qualifications:

  • Bachelor's degree in Clinical Research preferred. (New graduates are strongly encouraged to apply!)
  • Bachelor's Degree in Computer Science or health-related field required but Associates Degree and equivalent work experience will be considered.
  • Strong understanding of clinical research principles, methodologies, and regulatory requirements (e.g., GCP, FDA regulations).
  • Excellent organizational skills and meticulous attention to detail.
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
  • Strong written and verbal communication skills.
  • Ability to work independently and as part of a team in a fast-paced environment.
  • Proactive, self-motivated, and eager to learn.
  • Ability to prioritize tasks and manage time effectively.
  • Experience with electronic data capture (EDC) systems is a plus, but not required.

Why Join Atrium Health?

  • Exceptional Learning Environment: Gain hands-on experience in a comprehensive clinical research setting.
  • Mentorship and Growth: Benefit from direct mentorship and opportunities for professional development.
  • Impactful Work: Contribute to research that directly improves patient outcomes and advances medical knowledge.
  • Collaborative Culture: Work alongside dedicated and experienced professionals in a supportive team environment.
  • Comprehensive Benefits: Atrium Health offers a competitive benefits package.
Job ID: 479139312
Originally Posted on: 5/31/2025

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