The Clinical Research Nurse, under the guidance and supervision of the Principal Investigator (PI), ensures the integrity and quality of clinical trials are maintained and conducted in accordance w/ state, and local regulations, policies and procedures.

This position is primarily responsible for the accurate completion of visit procedures and collection of information from study patients according to protocols, and for protecting the health, safety, and welfare of research participants. In addition, the clinical trial nurse also acts as study coordinator for limited studies.

Essential Functions:

• Providing nursing care to research study patients:
• Ensures compliance with each study’s protocol by providing thorough review and documentation at each subject study visit
• Performs medical tests, including, but not limited to, vital signs, imaging studies, and electrocardiograms
• Administers investigational medications and performs patient assessments during clinic visits to determine presence of side effects; notifies Principle Investigator of findings/issues
• Provides patient education and medical information to study patients to ensure understanding of proper medication dosage, administration, and disease treatment
• Documents medical data in patient chart to capture protocol requirements
• Ensures site compliance with research protocols by reviewing all regulatory requirements to confirm implementation of appropriate methods, practices, and procedures for all research activities
• Nurse certification required

Qualifications:

• Minimum of a diploma from an accredited nursing school required; Bachelor of Nursing or other Science degree preferred
• Two (2) years of recent clinical nursing experience in a hospital, clinic or similar health care setting (Bachelor's degree may be substituted for one (1) year work experience) • Nursing competency skills per scope of practice (i.e., performing vital signs, nursing assessments, performing ECG/EKG, administering injections, etc.) •
• At least one (1) year clinical trials research experience preferred •
• Knowledge of medical terminology, drug calculation skills, clinical medicine, clinical trials and GCP concepts
• Detail oriented and meticulous in all aspects of work
• Ability to work well independently as well as in team environment
• Knowledge of GCP

Art der Stelle: Freie Mitarbeit, Minijob

Bewerbungsfrage(n):

• Besitzen Sie einen Führerschein der Klasse B und ein eigenes Fahrzeug?
• Arbeiten Sie bereits als freiberufliche Pflegekraft?
• Verfügen Sie über mindestens zwei Jahre Berufserfahrung als Pflegekraft?

Arbeitsort: Vor Ort

Bewerbungsfrist: 18.08.2025