Clinical Research Assistant: Research Institute Akron, OH

Clinical Research Assistant:
Research Institute job at Akron Children's. Akron, OH.

Full‑Time, 40 Hours/Week;
Monday to Friday, 8am - 4:30pm;
Hybrid (2‑3 Days/Week Onsite)

The Clinical Research Assistant (CRA) is a research professional reporting to the Clinical Research Support Team Supervisor and working with and under the direction of Clinical Research Coordinator/Clinical Research Nurse, and Clinical Principal Investigator (PI) on ongoing research studies. While the PI is ultimately responsible for the clinical trial, the CRA will support diverse clinical trials and research studies and may have roles across the entire research continuum in accordance with federal, state, and local regulations, Institutional Review Board (IRB) approvals and Akron Children's Hospital (ACH) policies and procedures.

The CRA plays a critical role in the conduct of the study and works collaboratively with the entire ACH Research team.

• Provide assistance in participant recruitment, screening, and follow‑up for clinical trials.
• Utilize Good Clinical Practice to ensure assigned study responsibilities are conducted in accordance with IRB and regulatory agency regulations.
• Ensure site compliance with research protocols by reviewing all regulatory requirements to confirm implementation of appropriate methods, practices, and procedures for all research activities.
• Complete timely and accurate data collection, documentation, entry, and reporting in both sponsor and ACH databases.
• Participate with the PI in scientific writing, preparation of research abstracts, manuscripts, presentations for academic audiences and grant applications.
• Transport, handle, process, and ship specimens while maintaining correct records of specimen management and transport coordination according to protocol.
• Collaborate with multidisciplinary teams across the enterprise, participate in team meetings and discussions to provide updates on project status and contribute to research strategic planning.
• Other duties as required.

• Knowledge of clinical trial protocols is preferred.
• Competency in interpreting medical charts and abstracting data is preferred.
• Knowledge of GCP, federal, state, and local regulations, including HIPAA policies and procedures.
• Competency in the use of Microsoft Office, Word, and Excel, Electronic Health Systems, EPIC and databases utilized in research or a willingness to learn and demonstrate proficiency within six months of hire.

• Education:
  
  Bachelor’s degree or bachelor’s eligible in a relevant field (e.g., Biology, Health Sciences, Data Science, Public Health, etc.) is required.
• Strong interest in clinical research and healthcare.
• Excellent communication skills, both written and verbal.
• Strong organizational abilities and attention to detail.
• Certification:
  None.
• Years of relevant experience:
  None.
• Experience in research is preferred.
• CITI Certification – certification is required within 90 days of hire.
• Ability to work independently as well as in a team environment.