Research | Clinical Research Coordinator II | Providence, Rhode

Research | Clinical Research Coordinator II | Providence, Rhode Island

Apply for the Research | Clinical Research Coordinator II | Providence, Rhode Island role at Panoramic Health
.

Advancing Care Through Innovation.

Position is on-site Monday - Friday in Providence, RI.

Nephrology Associates Inc 314 Taunton Ave, East Providence, RI 02914.

To learn more about Panoramic Science visit:

Come Join Panoramic's Science Division!

The Clinical Research Coordinator II leads the clinical research program at the site level: effectively recruiting and enrolling research patients under the principal investigator, always in compliance with institutional Standard Operating Procedures, protocol specifications, and good clinical practice. In addition, proactively develops and implements workflows to optimize recruitment, enrollment, and study execution.

• Read and understand assigned research protocols. Prescreen patients, train site staff on study purpose, record attendance, and evaluate resources needed to deploy the study.
• Proactively recruit eligible patients by communicating criteria and flagging them to physicians and clinic staff. Work with leadership to communicate study opportunities, meet targets with central research teams, document informed consent per ICH/GCP, and enter data per ALCOA principles.
• Prepare for monitoring visits:
  • All source documents organized and available.
  • Respond on time to monitor letters resolving outstanding items.
  • All prior queries closed.
  • Temperature and accountability logs current.
• Ongoing study oversight and management:
  • Plan visits per protocol schedule, avoid protocol deviations.
  • Coordinate space and resources with administration.
  • Report adverse events to IRB, sponsor, and management per guidelines.
  • Dispense and collect medication, maintain investigational product accountability.
  • Collect and process laboratory specimens per protocol.
  • Complete case report forms and tracking information accurately and on time.
  • Understand data collection instruments and collect data per protocol.
• Perform other duties as required, assigned, or requested.

• MA Certification preferred.
• Bachelor’s degree in a health-related field preferred.
• Good Clinical Practice and/or ITIA Certification preferred.
• ACRP or Socra Certification preferred.
• Bilingual preferred (Spanish).
• Minimum 3‑5 years of clinical research experience.
• Experience in CKD, nephrology, or vascular access preferred.
• Knowledge of medical terminology and research.
• Self‑motivated individual who drives patient safety, enrollment targets, timely data entry, and GCP adherence.
• Excellent interpersonal and communication skills.
• Flexibility, organizational skills, and attention to detail.
• Knowledge of and adherence to GCP, IATA, and FDA regulations.
• Ability to perform basic clinical procedures such as blood work, vitals, height, weight, etc.
• Ability to perform ECGs.
• Ability to multitask and handle high patient volume across studies.
• Open to a flexible schedule.

The company is committed to the principles of equal employment. We comply with all federal, state, and local laws providing equal employment opportunities. We maintain a work environment free of harassment, discrimination, or retaliation based on protected status, and fulfill this policy across all aspects of employment, including recruiting, hiring, placement, transfer, training, promotion, pay, compensation, termination, and other employment terms.

For more information, please visit