Columbia, Missouri – PRN Nurse Practitioner

Reports to: Principle Investigator

Position Summary:

Nurse practitioner to support Principal Investigator for clinical research studies.  Apply medical techniques and principles under the direction of a physician for the successful execution of clinical research studies.

Duties and Responsibilities:

  • Knowledge of protocol and visit requirements for assigned studies.
  • Ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements;
  • Maintain security and confidentiality.
  • Notify Principal Investigator of patient non-compliance or other drug-related problems.
  • Read laboratory values and report abnormal values to investigator and patient.
  • Experience applying the following regulations and guidelines: GCP, HIPPA, The Protection of Human Research Subjects, OSHA
  • Maintain certification in CPR/ACLS
  • Ensure the safety and well-being of all study subjects throughout the study.
  • Regulatory document review;
  • Verification and review and reporting of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;

Qualifications:

  • Master’s Degree in Nursing and graduation from a Nurse Practitioner Program;
  • Strong communication skills both written and verbal;
  • Ability to build strong rapport with medical site staff;
  • Excellent communicative and social skills, accuracy, perseverance and organizational skills;

Please send your resume to resumes@biopharmaservices.com