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Research Nurse

Role overview

Qualifications

  • Bachelor's degree or equivalent in the clinical/medical field
  • Valid nursing license (RN, LVN, LPN)
  • 0 to 2 years of relevant experience
  • Basic understanding of the clinical research process

Responsibilities

  • Travel 50% of the time to conduct clinical studies according to regulations
  • Provide medical care to patients, ensuring their safety
  • Perform defined study activities such as informed consent and protocol procedures
  • Record patient information and results, ensuring accuracy and compliance

Key facts

Other skills

  • Decision Making
  • Detail Oriented
  • Social Skills
  • Organizational Skills
  • Communication
  • Problem Solving

About the company

Thermo Fisher Scientific logo

Thermo Fisher Scientific

About Thermo Fisher Scientific Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. For more information, please visit www.thermofisher.com.

Company details

Company size10001

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Job description

Work Schedule

Environmental Conditions

Job Description

Join Us as a Clinical Research Nurse – Make an Impact at the Forefront of Innovation

The Clinical Research Nurse is a hybrid travel role. The CRN joins a virtual site operations SWAT team to support clinical studies at our trialmed and affiliated sites. Interacts with the research site team and interdepartmental staff to ensure positive interactions with patients at site for study planning, from initiation to closeout.

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

What You'll Do:
•Expected to travel 50% of the time. Conduct clinical studies according to FDA/GCP and ICH regulations and guidelines.
• Provide medical care to patients, always ensuring patient safety comes first.
• 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 timely completion.
• Gather 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 0 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:
• Basic 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
• Possess decision-making, negotiation and influencing skills
• Good communication skills and English fluency will be an advantage
• Great organizational skills
• Essential proficiency in basic computer applications
• Great 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.
 

Compensation and Benefits

The hourly pay range estimated for this position based in Minnesota is –.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

  • A choice of national medical and dental plans, and a national vision plan, including health incentive programs

  • Employee assistance and family support programs, including commuter benefits and tuition reimbursement

  • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy

  • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan

  • Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

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