Clinical Research Nurse- Full Time Days

Work Schedule

12 hr shift/days

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards

Job Description

Job Description

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.

Location/Division Specific Information

Our global Clinical Operations colleagues within our PPD® clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts. Together, we help clients define and develop clinical programs, minimize delays, and execute high-quality, cost-efficient clinical studies.

Discover Impactful Work:

Supports the Clinic in the overall conduct of multiple, ongoing clinical trials involving an in-patient setting, ensuring patient safety and cooperation during the study process.

A day in the Life:

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

Keys to Success:

Education

• ADN from an accredited institution/active RN or LVN licence to practice

Experience

• The Clinical Research Nurse supports the Clinic in the overall conduct of multiple, ongoing clinical trials involving oral surgery patients in an in-patient setting, ensuring patient safety and cooperation during the study process. Responsibilities include: - Reviews inclusion/exclusion criteria with patients to ensure eligibility to participate in study. Interacts with Primary Investigator for inclusion/exclusion review of patient data - Reviews and witnesses the consenting process for subjects. - Ensures the safety of patients by monitoring and assessing AEs, if any, and communicating potentially serious findings to physician - Performs all procedures in the recovery area (i.e., check-ins, gauze management, administration of drug, blood draws, ECGs, vital signs, etc.) - Monitors staff to assure adherence to Good Clinical Practices, ICH, FDA, and OSHA guidelines Education and Experience: RN degree from an accredited institution Active license to practice in the state of Nevada 1 year experience as RN Knowledge, Skills and Abilities: Ability to function with multiple types of individuals and work in a team environment while maintaining a positive attitude Strong planning and organizational capabilities to manage multiple tasks and study groups at one time Basic computer skills Willingness and ability to learn administer investigational drugs including oral, intravenous, topical, or other approved method 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. Ability to work a flexible schedule to meet the study needs of the Clinic Good handwriting and attention to detail Excellent verbal and written communication skills Pharmaceutical Product Development, LLC is firmly committed to Equal Employment Opportunity (EEO) and prohibits employment discrimination for employees and applicants based on age, race, color, pregnancy, gender, gender identity, sexual orientati