Clinical data Work, Jobs in Edinburgh, Edh (with Salaries)

Clinical Research Associate II
IQVIA —Livingston
- Full-time
- No degree
- Recruiting
Clinical Data Manager
Charles River Laboratories —Tranent
- Up to £40,000 a year
- Full-time
- Computer literacy
- Bachelor's degree
- Organisational skills
9d
Clinical Data Programmer
Charles River Laboratories —Tranent
- £30,000 - £34,000 a year
- Weekend availability
- Computer literacy
- Bachelor's degree
- Mentoring
9d
Medical Records Summariser/Workflow Administrator
Ladywell Medical Centre East —Edinburgh
- From £27,061 a year
- Part-time
- Hybrid work
- Microsoft Excel
- SQL
- Analysis skills
- Free parking
- Store discount
Quick apply
10d
Scientific Associate 1
Charles River Laboratories —Tranent
- £28,789.76 a year
- Full-time
- Computer literacy
- No degree
- Computer skills
11d
Scientific Associate
Charles River Laboratories —Tranent
- £28,789.65 a year
- Full-time
- Laboratory experience
- No degree
- Communication skills
5d
Data Acquisition Specialist - External Data (Remote - UK)
IQVIA —Livingston
- Full-time
- Remote
- Computer Science
- English
- Bachelor's degree
- Work from home
11d
Data Scientist
Optos —Dunfermline
- Doctoral degree
- Computer Science
- Engineering
5d
Clinical Project Manager x 2
Charles River Laboratories —Tranent
- £35,000 - £40,000 a year
- Full-time
- Master's degree
- Bachelor's degree
- Travel
2d
R & D Scientist (Haematology)
AliveDx —Penicuik
- Full-time
- Data analysis skills
- Laboratory experience
- No degree
Medical Writer - Publications
Real Chemistry —Edinburgh
- Hybrid work
- Microsoft Powerpoint
- Doctoral degree
- Master's degree
- Annual leave
Patient Care Advisor (Receptionist)
Leith Links Medical Group —Edinburgh
- £13.86 - £15.05 an hour
- Full-time
- Computer literacy
- GP surgery experience
- Microsoft Office
Quick apply
8h
Suicide Prevention Officer
Change Mental Health —Edinburgh
- £30,768.10 a year
- Part-time
- Hybrid work
- Supervising experience
- Project management
- Travel
- Employee assistance programme
- Employee discount
Quick apply
Admin Assistant – Events & Facilities
NHS Scotland —Edinburgh
- £29,103 - £31,409 a year
- Full-time
- Hybrid work
- Customer service
- Communication skills
- Teaching
- Annual leave
7d
Senior Scientist / Associate Principal Scientist – Biophysics & Protein Science
Concept Life Sciences —Edinburgh
- Doctoral degree
- No degree
- Travel
- Free parking
Technology Transfer Scientist
AliveDx —Penicuik
- Full-time
- Engineering
- Continuous improvement
- Organisational skills
- Annual leave
6d
Implementation Consultant
System C —Edinburgh
- Full-time
- Software troubleshooting
- Travel
- Communication skills
Occupational Health Advisor
OH3 Ltd —Edinburgh
- Part-time
- Case management
- Travel
- Mentoring
- Paid training
- Health & wellbeing programme
Quick apply
9h
Specialist Analytical Development
NextPharma GmbH —Livingston
- Full-time
- Data analysis skills
- Analysis skills
- Continuous improvement
- Life insurance
Validation Technician
AliveDx —Penicuik
- Full-time
- Computer literacy
- Continuous improvement
- Organisational skills
- Annual leave
12d

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clinical data jobs near edinburgh, edh

Clinical Research Associate II

IQVIA -
Livingston

Apply Now

Job details

Full-time

Qualifications

Clinical research
Stakeholder liaison
Filing
Recruiting
Clinical compliance monitoring
Good Clinical Practice (GCP)
Good Clinical Practice (ICH-GCP) guidelines
Research participant recruitment coordination

Full job description

Livingston, United Kingdom | Full time | Field-based | R1559650

Join IQVIA on our mission to accelerate innovation for a healthier world!

IQVIA UK’s cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates in Scotland.

Why IQVIA?

Career development opportunities to grow as we grow
AI‑powered career advancement through our internal talent marketplace, Career Connections
Flexible working to assist work–life balance and professional success
Well‑being support covering your physical, mental, and financial health

Awards

2026 "Glassdoor Best Place to Work in the UK"
#1 in category - 2026 Fortune® World’s Most Admired Companies™ list (for the FIFTH consecutive year!)
Brandon Hall Excellence Award for Learning & Development

Responsibilities

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
Collaborate and liaise with study team members for project execution support as appropriate

Requirements

Requires at least 2 years on-site monitoring experience of interventional studies
Degree in scientific discipline or health care or equivalent industry experience
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Ability to establish and maintain effective working relationships with coworkers and clients
Full UK right to work required, this position is not eligible for visa sponsorship

Apply today and forge a career with greater purpose, make an impact, and never stop learning!

#LI-ADAMTHOMPSON

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Field-based

You’ll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impact.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

Refine Your Search

clinical data jobs in edinburgh, edh

Clinical Research Associate II

Clinical Data Manager

Clinical Data Programmer

Medical Records Summariser/Workflow Administrator

Scientific Associate 1

Scientific Associate

Data Acquisition Specialist - External Data (Remote - UK)

Data Scientist

Clinical Project Manager x 2

R & D Scientist (Haematology)

Medical Writer - Publications

Patient Care Advisor (Receptionist)

Suicide Prevention Officer

Admin Assistant – Events & Facilities

Senior Scientist / Associate Principal Scientist – Biophysics & Protein Science

Technology Transfer Scientist

Implementation Consultant

Occupational Health Advisor

Specialist Analytical Development

Validation Technician

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