Clinical Research Nurse II

at  Thermo Fisher Scientific

ENVIRONMENTAL CONDITIONS

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description

TO BE CONSIDERED FOR THIS EXCITING OPPORTUNITY YOU WILL REQUIRE THE FOLLOWING SKILLS AND EXPERIENCE:

• A qualified Nurse, a registration with no limitations to practice within the Nursing and Midwifery Council (Adult)
• A passion for the Clinical Research industry
• Well-developed interpersonal and communication skills, the ability to work in a cross functional team
• A patient focussed attitude
  Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
  Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

• Completing all relevant clinical competency training assessments and attending all relevant research study protocol training and completing all mandatory training, according to the Synexus COPs/SOPs
• Performing all visits, observations, safety reporting and interventions with participants in accordance with procedures and schedule of the study protocol, company SOPs and policies
• Carrying out pre-screens efficiently and effectively to optimise patient recruitment
• Encouraging patients to continue within the study, and to participate in future trials
• Collecting, records, verifying and entering study data into the source notes, CRF/eCRF and all associated paperwork with a high degree of accuracy
• Ensuring that all data queries are acted upon in a timely and efficient manner
• Promoting and nurturing a welcoming, professional, and pleasant environment for staff and participants
• Participating in multidisciplinary meetings
• Initiating emergency action when required e.g., cardiac arrest, anaphylaxis management, fire, or critical incidents