Medical Device Nurse jobs

*This position is a 12 month fixed term contract*

What You'll Do:

• Conduct clinical studies according to FDA/GCP and ICH regulations and guidelines.
• Provide medical care to patients, always ensuring patient safety comes first.
• Schedule subject visits within protocol windows, ensuring scheduling capacity is maximized.
• Perform all defined study activities (i.e., informed consent, screening, and protocol procedures which include but are not limited to vital signs, pregnancy tests, height, weight, ECGs, etc.).
• Record all patient information and results from tests as per protocol on required forms.
• Complete IP accountability logs and associated information when required.
• Report suspected non-compliance to relevant site staff.
• Ensure that IRB approval is obtained prior to study initiation and that IRB requirements are met throughout the study.
• Promote the company and build a positive relationship with patients to ensure retention.
• Attend site initiation meetings and all other relevant meetings to receive training on the protocol.
• Call patients, handle patient bookings, and perform follow-up calls when required to confirm bookings or provide information or results.
• Log and complete information on sponsor systems, ensuring accuracy (i.e., case report forms, EDC, etc.) and completing it within the required timeframe.
• Gather and maintain source documents, update patient files and notes, always ensuring relevant and up-to-date information is recorded.
• Adhere to company COP/SCOP.
• Dispose of waste according to standards and assist in maintaining a neat appearance of the facility when required.

Education and Experience Requirements:

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification in the clinical / medical field
• Must hold a valid nursing license (RN, LVN, LPN) within the country operating. Must be registered with local health care authority.
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years’)

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills, Abilities:

• Solid understanding of the clinical research process (i.e., GCP, SOPs, informed consent, safety monitoring, etc.)
• Capable of working independently, analyzing and working with attention to detail, processing and

prioritizing sensitive complex information and problem solving

• Demonstrated ability to exercise discretion and sound judgement
• Posses decision-making, negotiation and influencing skills
• Good communication skills and English fluency will be an advantage
• Great organizational skills
• Good proficiency in basic computer applications
• Excellent interpersonal skills to work in a team environment

Working Environment:
Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:

• Work is performed in an office/ laboratory and/or a clinical environment.
• Exposure to biological fluids with potential exposure to infectious organisms.
• Exposure to electrical office equipment.
• Personal protective equipment required such as protective eyewear, garments and gloves.
• Occasional travel, may be domestic or international.

Why join us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthroughs.