Clinical Research Nurse (On-site)

Cardiff, Wales, United Kingdom

12/15/2024

Work Schedule

Standard (Mon-Fri)

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.)

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 – To enable 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.

Alongside clinical research through our PPD® clinical research portfolio, our work in Accelerated Enrollment Solutions optimizes each step of the patient journey in clinical trials, such as securing sites and recruiting patients, allowing for more patients to participate in clinical research. Your determination to put patients at the heart of every decision will improve health outcomes that people and communities depend on – now and in the future.

Are you passionate about improving patient’s lives for the better?

We are currently looking to recruit a Clinical Research Nurse for our Synexus Clinical Research site in Cardiff, United Kingdom

We pride ourselves on being the “Patient’s choice for clinical research” and our Nursing teams are directly involved with ensuring a continuity of care for patients during the studies.

Working days, Monday to Friday, 37 hours a week, a Clinical Research Nurse is responsible for nursing activities related to clinical trials across a wide and diverse range of therapeutic areas.

Key responsibilities for a Clinical Research Nurse are as follows:

• 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
  
  

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.