Clinical trial Work, Jobs in Glasgow, Glg (with Salaries)

Clinical Research Nurse
Thermo Fisher Scientific —Glasgow
- Full-time
- Hospital
- Computer literacy
- English
Project Assistant - Clinical Safety & Pharmacovigilance (office based in Stirling)
Medpace, Inc. —Stirling
- Full-time
- English
- Administrative experience
- Bachelor's degree
- Annual leave
- Work from home
Clinical Safety Coordinator
Medpace, Inc. —Stirling
- Full-time
- Microsoft Office
- Bachelor's degree
- In-person
- Annual leave
- Work from home
Experienced Regulatory Submissions Coordinator
Medpace, Inc. —Stirling
- Full-time
- Bachelor's degree
- In-person
- Communication skills
- Annual leave
- Work from home
Huntington's Disease Specialist
Scottish Huntington's Association —Paisley
- £34,543 - £38,216 a year
- Hybrid work
- Driving
- Communication skills
Contamination Control Manager
Piramal Healthcare UK Limited —Grangemouth
- Engineering
- Master's degree
- Bachelor's degree
7h
Senior Q&V Specialist
Piramal Healthcare UK Limited —Grangemouth
- Computer literacy
- Continuous improvement
- Computer skills
14d
Senior Research Nurse - Glasgow Clinical Research Facility (GCRF)
NHS Scotland —Glasgow
- £43,231 - £52,679 a year
- Full-time
- No degree
- Recruiting
- Leadership
- Annual leave
- Employee assistance programme
13d
Consultant Clinical Oncologist specialising in Urology and Skin Cancer
NHS Scotland —Glasgow
- £111,430 - £148,064 a year
- Full-time
- Teaching
3d
Qualified Person (QP)
Catalent —Bathgate
- Full-time
- Bachelor's degree
- Organisational skills
- Communication skills
- Free parking
- Employee assistance programme
10d
Cancer Care Pharmacist Specialist B7
NHS Scotland —Glasgow
- £52,845 - £61,466 a year
- Full-time
- Annual leave
- Employee assistance programme
6d
Manager, Process Excellence
Catalent —Bathgate
- Full-time
- Engineering
- Analysis skills
- Bachelor's degree
- Free parking
- Employee assistance programme
10d
Senior Manufacturing Technician
Piramal Healthcare UK Limited —Grangemouth
- Mentoring
- Communication skills
9d

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Project Assistant - Clinical Safety & Pharmacovigilance (office based in Stirling)
Medpace, Inc. —Stirling
Assist with case processing and reporting activities as delegated. Provide day to day project support to the clinical safety department.

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clinical trial jobs near glasgow, glg

Clinical Research Nurse

Thermo Fisher Scientific -
Glasgow

Apply Now

Job details

Full-time

Qualifications

Care record keeping
Healthcare research operations
Clinical research
Clinical record keeping
Computer literacy
Patient appointment coordination
Case note recording
Case record updates
English
Bachelor's degree
Appointment booking and call handling
Patient care
Data entry
Organisational skills
Good Clinical Practice (GCP)
Patient record updating
Communication skills
Good Clinical Practice (ICH-GCP) guidelines
Research participant recruitment coordination

Full job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

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

Job Description

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

The Clinical Research Nurse II conducts multiple ongoing clinical trials involving patients or healthy volunteers/subjects. Completes all paperwork required to capture all data as specified by a study protocol, and for ensuring subject safety, understanding, and cooperation during the study process. Interacts with the research site team and other interdepartmental staff. Engages in the entire site operations process, which includes recruitment, enrollment, and retention of study participants.

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.

This is a full time, permanent opportunity based onsite at our Bellshill site

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.
Has some Nursing experience gained within a hospital or clinical setting. Training and development will be provided!

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.

Apply Now

Refine Your Search

clinical trial jobs in glasgow, glg

Clinical Research Nurse

Project Assistant - Clinical Safety & Pharmacovigilance (office based in Stirling)

Clinical Safety Coordinator

Experienced Regulatory Submissions Coordinator

Huntington's Disease Specialist

Contamination Control Manager

Senior Q&V Specialist

Senior Research Nurse - Glasgow Clinical Research Facility (GCRF)

Consultant Clinical Oncologist specialising in Urology and Skin Cancer

Qualified Person (QP)

Cancer Care Pharmacist Specialist B7

Manager, Process Excellence

Senior Manufacturing Technician

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