Clinical Research Nurse II - Impactful, 12-Month Contract

Thermo Fisher Scientific Inc.; Manchester; On-site; GBP 36,000 - 48,000; Full time

Job summary

Thermo Fisher Scientific is seeking a Clinical Research Nurse II to conduct multiple trials, ensure patient safety, and manage data collection per protocol. You will interact with site teams, oversee recruitment and retention, and support study activities across the research site.

This 12-month fixed-term contract offers exposure to FDA/GCP/ICH guidelines, hands-on clinical procedures, and collaboration with sponsors.

Qualifications

• Bachelor’s degree or equivalent in the clinical/medical field.
• Must hold a valid nursing license (RN, LVN, LPN) within the country operating.
• 2+ years of relevant clinical experience or equivalent.

Responsibilities

• Conduct clinical studies according to FDA/GCP and ICH regulations and guidelines.
• Provide medical care to patients with safety as a priority.
• Schedule subject visits within protocol windows to maximize capacity.
• Record patient data and test results on required forms.
• Complete IP accountability logs and log data into sponsor systems as required.
• Report suspected non-compliance to site staff.
• Ensure IRB approval is obtained and maintained.
• Promote the company and build patient relationships to aid retention.
• Attend site initiation and protocol training meetings.
• Call patients for bookings and follow-ups as needed.
• Maintain source documents and up-to-date patient records.

Skills

GCP knowledge

Informed consent

Patient safety

Communication skills

Attention to detail

MS Office

Education

Bachelor’s degree in clinical/medical field

Tools

EDC systems

Job description

Thermo Fisher Scientific is seeking a Clinical Research Nurse II to conduct multiple trials, ensure patient safety, and manage data collection per protocol. You will interact with site teams, oversee recruitment and retention, and support study activities across the research site.

This 12-month fixed-term contract offers exposure to FDA/GCP/ICH guidelines, hands-on clinical procedures, and collaboration with sponsors.