Clinical Research Coordinator (LPN) In-person

Smith Allergy and Asthma

Cortland, NYFull-timePosted May 5, 2026

Behavioral Health Market Context

Latest national behavioral health workforce report (2026-W26)New York behavioral health workforce newsBrowse all behavioral health workforce news
Apply Nowvia Health Jobs Nationwide

Qualifications

  • •Licensed Practical Nurse (LPN) credential in the United States
  • •Basic knowledge of clinical research principles and regulatory requirements
  • •Experience in patient care and clinical procedures
  • •Strong organizational and communication skills
  • •Ability to work collaboratively in a multidisciplinary team environment
  • •The Clinical Research Coordinator (LPN) utilizes clinical nursing skills daily to perform patient assessments, administer treatments, and monitor patient safety during trials
  • •Additionally, proficiency with electronic data systems supports accurate data entry and reporting, which is critical for the integrity and success of clinical trials
  • •4 more items(s)

Responsibilities

  • •The Clinical Research Coordinator (LPN) plays a pivotal role in managing and overseeing clinical trials to ensure they are conducted in compliance with regulatory standards and study protocols
  • •This position involves coordinating patient recruitment, data collection, and communication between study participants and the research team to facilitate smooth trial operations
  • •The coordinator ensures accurate documentation and reporting of clinical data, maintaining the integrity and confidentiality of patient information
  • •By collaborating closely with investigators, sponsors, and regulatory bodies, the coordinator helps advance medical research and contributes to the development of new treatments
  • •Ultimately, this role supports the successful execution of clinical studies that improve patient outcomes and advance healthcare knowledge
  • •Coordinate and manage daily clinical trial activities including patient screening, enrollment, and follow-up visits
  • •Ensure compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements
  • •Collect, record, and maintain accurate clinical data and patient records in electronic data capture systems
  • •Serve as the primary liaison between patients, investigators, and sponsors to facilitate communication and resolve issues
  • •Monitor patient safety and report adverse events promptly according to protocol and regulatory guidelines
  • •Schedule and conduct study visits, including obtaining informed consent and performing clinical assessments
  • •Assist in the preparation and submission of regulatory documents and study reports
  • •Maintain inventory of study supplies and ensure proper storage of investigational products
  • •Strong organizational skills are essential for managing multiple study protocols, scheduling visits, and maintaining accurate documentation
  • •Effective communication skills facilitate clear interactions with patients, investigators, and sponsors, ensuring all parties are informed and engaged
  • •Knowledge of regulatory guidelines and clinical research processes ensures compliance and ethical conduct throughout the study lifecycle
  • •13 more items(s)
Apply for this Position

More Jobs