Clinical Research Nurse Per Diem Day

Thermo Fisher Scientific•Las Vegas, NV

7d•Onsite

About The Position

Join us as a Clinical Research Nurse - And take charge of overseeing nursing staff, coordinating patient care, managing day-to-day clinical operations, ensuring adherence to healthcare standards, and fostering a collaborative and efficient work environment. At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Requirements

ADN from an accredited institution/active RN or LVN license to practice
1 year experience as RN or LVN
Technical positions may require a certificate
Previous experience to provides the knowledge, skills, and abilities to perform the job (comparable to at least 6 years). Bachelor’s degree preferred.
Ability to work well in a team environment and interact with all levels of staff, clients, and subjects in a positive and professional manner
Strong planning and organizational capabilities to manage multiple tasks and study groups at one time
Basic computer skills, good handwriting and attention to detail
Willingness and ability to administer investigational drugs or test investigational devices intravenously, topically, or by other approved methods of dosing
Willingness and ability to learn and perform a variety of technical procedures such as drawing blood, processing and harvesting lab specimens, taking vital signs, performing ECGs, etc.
Excellent verbal and written communication skills.
Ability to respond to medical emergency scenarios, in accordance with ACLS guidance, established emergency protocols, and Investigator instructions

Nice To Haves

Bachelor’s degree preferred.
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.

Responsibilities

Review inclusion/exclusion criteria with patients to ensure eligibility to participate in study.
Interact with Principal Investigator for inclusion/exclusion review of patient data.
Review and witness the consenting process for subjects.
Prepare study-specific documents for applicable study visit.
Ensure the safety of patients by monitoring and assessing AEs, if any, and communicating potentially serious findings to investigators.
Perform all procedures in the treatment areas (i.e., check-ins, gauze management, administration of drug, blood draws, ECGs, vital signs, etc.).
Monitor staff to assure adherence to GCP, ICH, FDA, and OSHA guidelines.
Attend initiation meetings when necessary to obtain study process clarification.
Monitor and continuously evaluates the overall research experience of each patient to assure a positive experience.
Perform other study-related duties as qualified by documented training.