Clinical Research Nurse

5 hours ago

Chula Vista, California, United States ProSciento, Inc Full time
Job Summary

ProSciento, Inc is seeking a highly skilled Clinical Research Nurse to join our team. The successful candidate will be responsible for managing all study-related clinical nursing procedures according to the study protocol and providing nursing care under appropriate supervision for subjects enrolled in clinical trials.

Key Responsibilities
  • Administer prescribed study medications, perform phlebotomy, draw blood samples, monitor vital signs, and/or perform other specialized nursing procedures as appropriate to the specific needs of the study and individual subjects.
  • Start peripheral intravenous lines using gauge 18 1 1⁄4" and double lumen catheter gauge 18 1 3⁄4" without use of tourniquets as per specific study protocol.
  • Perform detailed review of subject's current meds and enter information appropriately in source document as indicated.
  • Administer concomitant medications as indicated or prescribed.
  • Participate in day-to-day clinical activities and procedures ensuring efficient workflow and adequate care and treatment of research subjects.
  • Complete study source documents for area of responsibility such as c-mar, fluid sheet, AE, and con med review.
  • Monitor and record subject response to treatment. Query subjects on adverse events/serious adverse events during study. Complete study specific subject information serious event intake form.
  • Resolve study source document discrepancies.
  • Assist in keeping adequate stock of consumable clinical inventory.
  • Manage or assist with training of new hires evaluating skills maintaining crash cart etc.
  • Provide supervision for research assistant and clamp tech staff in the performance of nursing related protocols involved in studies including assistance in training on the specifics of phlebotomy and blood draws proper care of specimens and properly obtaining urine samples.
  • Partner with the human resources department with respect to completion of procedures and processing including documentation and logistics for staff who have had exposure incidents.
  • Manage or assist with keeping employee immunizations up to date (TB Hep B) including maintaining associated documents.
  • Develop synopses for nurse and research assistant use for each clinical trial.
  • Participate in training of other nurses and/or new hires in pertinent aspects of each protocol.
  • Assist in the training of research assistant staff for protocol-related and clinical procedure activities.
Requirements
  • Bachelor of Science in nursing as well as two years RN critical/acute care experience in a hospital clinical research and/or similar environment or an equivalent combination of medical education training certifications and/or experience.
  • Excellent IV skills necessary. Knowledge of immunizations for employers including record-keeping. Ability to work evening and overnight shifts as required. Ability to conform to a 12-hour alternative work week shift schedule. Exercises calm judgment and actions under pressure. Demonstrates initiative and problem-solving skills. Able to respect subject confidentiality and blinding procedures. Understands medical terminology and calculations. Demonstrates a strong attention to detail with superior organizational skills. Under general supervision exercises judgment in accordance with well-defined policies procedures and techniques. Ability to self-monitor progress and complete assigned tasks independently.
  • Active Registered Nurse (RN) license in the State of California. BLS & ACLS certification is required and may be provided by the company.

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