Clinical Research Nurse- Full Time Days

Work Schedule

12 hr shift / days

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards

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

Experience

Knowledge, Skills, Abilities

Previous experience

Physical Requirements / Work Environment

Benefits

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!