Clinical Research Nurse, Enrollment

Thermo Fisher Scientific•Las Vegas, NV

About The Position

Join Us as a Clinical Research Nurse – Make an Impact at the Forefront of Innovation The Clinical Research Nurse conducts at least one ongoing clinical trial that may involve patients or healthy volunteers. Interacts with the research site team and interdepartmental staff to ensure positive interactions with patients at site for study planning, from initiation to closeout. We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. What You'll Do: Conduct clinical studies according to FDA/GCP and ICH regulations and guidelines. Provide medical care to patients, always ensuring patient safety comes first. Perform all defined study activities (i.e., informed consent, screening, and protocol procedures which include but are not limited to vital signs, pregnancy tests, height, weight, ECGs, etc.). Record all patient information and results from tests as per protocol on required forms. Complete IP accountability logs and associated information when required. Report suspected non-compliance to relevant site staff. Ensure that IRB approval is obtained prior to study initiation and that IRB requirements are met throughout the study. Promote the company and build a positive relationship with patients to ensure retention. Attend site initiation meetings and all other relevant meetings to receive training on the protocol. Call patients, handle patient bookings, and perform follow-up calls when required to confirm bookings or provide information or results. Log and complete information on sponsor systems, ensuring accuracy (i.e., case report forms, EDC, etc.) and timely completion. Gather source documents, update patient files and notes, always ensuring relevant and up-to-date information is recorded. Adhere to company COP/SCOP. Dispose of waste according to standards and assist in maintaining a neat appearance of the facility when required.

Requirements

Bachelor's degree or equivalent and relevant formal academic / vocational qualification in the clinical / medical field
Must hold a valid nursing license (RN, LVN, LPN) within the country operating. Must be registered with local health care authority.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years’). In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Basic understanding of the clinical research process (i.e., GCP, SOPs, informed consent, safety monitoring, etc.)
Capable of working independently, analyzing and working with attention to detail, processing and prioritizing sensitive complex information and problem solving
Demonstrated ability to exercise discretion and sound judgement
Possess decision-making, negotiation and influencing skills
Good communication skills and English fluency will be an advantage
Great organizational skills
Essential proficiency in basic computer applications
Great interpersonal skills to work in a team environment

Responsibilities

Conduct clinical studies according to FDA/GCP and ICH regulations and guidelines.
Provide medical care to patients, always ensuring patient safety comes first.
Perform all defined study activities (i.e., informed consent, screening, and protocol procedures which include but are not limited to vital signs, pregnancy tests, height, weight, ECGs, etc.).
Record all patient information and results from tests as per protocol on required forms.
Complete IP accountability logs and associated information when required.
Report suspected non-compliance to relevant site staff.
Ensure that IRB approval is obtained prior to study initiation and that IRB requirements are met throughout the study.
Promote the company and build a positive relationship with patients to ensure retention.
Attend site initiation meetings and all other relevant meetings to receive training on the protocol.
Call patients, handle patient bookings, and perform follow-up calls when required to confirm bookings or provide information or results.
Log and complete information on sponsor systems, ensuring accuracy (i.e., case report forms, EDC, etc.) and timely completion.
Gather source documents, update patient files and notes, always ensuring relevant and up-to-date information is recorded.
Adhere to company COP/SCOP.
Dispose of waste according to standards and assist in maintaining a neat appearance of the facility when required.