Clinical Research Nurse Specialist

vor 2 Monaten


Ingelheim am Rhein, Rheinland-Pfalz, Deutschland Georgetown University in Qatar Vollzeit
Job Summary

We are seeking a highly skilled Clinical Research Nurse I to join our team at Georgetown University in Qatar. The successful candidate will be responsible for managing the overall coordination of assigned clinical trials throughout the trial lifecycle.

Key Responsibilities
  • Manage the overall coordination of assigned clinical trials throughout the trial lifecycle.
  • Collaborate with investigators and more senior study team members by participating in recruitment and selection of study participants, documenting and collecting data to support protocol screening and determine compliance with eligibility requirements.
  • Interface with study participants and obtain and document informed consent according to protocol, institutional policies, and regulatory guidelines.
  • Coordinate or conduct study-related procedures and assessments while maintaining protocol integrity and patient safety and in accordance with Good Clinical Practice (GCP) guidelines.
  • Assist in the assessment, management, and coordination across the continuum of care (outpatient, inpatient, and home) including triage of phone calls, symptom management, and proactive patient communication.
  • Document all study-related activity, including medical data, in the participant's medical record and when applicable, the patient research chart, in compliance with protocol and sponsor requirements.
  • Conduct follow-up with study participants in accordance with established standards and protocols.
  • Provide clinical and administrative nursing support to Clinical Research Coordinator and Clinical Research Nurse positions.
  • Ensure site compliance with research protocols by reviewing all regulatory requirements to confirm implementation of appropriate methods, practices, and procedures for all research activities.
  • Coordinate collection of research specimens per protocol requirements with Clinical Research Coordinators, providing patient education about clinical trial participation, treatment, potential side effects, and required testing.
  • Schedule/conduct in-service training for appropriate staff on assigned clinical trials.
  • Regularly update the Clinical Trials Management System (CTMS) with patient information and key dates to support responsible financial management of clinical trials with Clinical Research Coordinators.
  • Collaborate with Data Coordinator(s) to assure the documentation for the clinical trial is complete and accurate, assisting with query resolution in a timely manner.
  • Document and report serious adverse events per protocol and institutional policy.
  • Act as a liaison with hospital staff, physicians, IRB, review committees, clinical research finance team, and auditors; Act as a liaison with sponsors during study start-up activities and participate in site initiation visits, monitoring visits, and audits.
  • Identify potential barriers to patient and physician participation in clinical trials; develop and implement methods to alleviate those barriers.
  • Actively participate in meetings, task forces, and committees as assigned.
  • Perform all duties in accordance with applicable laws and regulation and adhere to Georgetown University Medical Center's philosophies, policies, and SOPs.
  • Work in compliance with Human Subject Protection, patient confidentiality/HIPAA, and GCP.
Work Interactions
  • Clinical Operations Team Manager
  • Disease Group members: Principal Investigators, Physicians, Clinicians
  • Lombardi Clinical Trials Office (CTO) members: Clinical Research Nurses, Clinical Research Coordinators, Data Coordinators, Regulatory Coordinators, Laboratory Technicians
  • External department clinicians and staff: Infusion Nurses, Oncology Pharmacists, hospital staff
  • Clinical trial sponsors, auditors, and study monitors
Requirements and Qualifications
  • Bachelor's degree, BLS certification, and RN license in the District of Columbia
  • Three to five (3-5) years nursing experience in a hospital, clinic, or similar health care setting
  • Up to two (2) years of clinical research experience
  • Strong candidates exhibit: Knowledge of clinical research, research processes, and Good Clinical Practice (GCP) Excellent verbal and written communication skills Excellent organizational skills and attention to detail Reliable and able to prioritize competing responsibilities


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