Clinical study manager Work, Jobs in Edinburgh, Edh (with Salaries)

Freelance Site Activation Specialist (Study Start-Up / Regulatory Submissions) – UK Remote
IQVIA —Edinburgh
- Full-time
- Remote
- English
- Bachelor's degree
- Communication skills
- Work from home
2d
Product Development Scientist
AliveDx —Penicuik
- Full-time
- Data analysis skills
- Laboratory experience
- No degree
- Employee discount
13d
Clinical Data Manager - FSP (Homebased - UK)
IQVIA —Livingston
- Full-time
- Remote
- Bachelor's degree
- Quality control
- Work from home
13d
Advocacy Worker
Partners in Advocacy —Edinburgh
- £25,392 a year
- Full-time
- Hybrid work
- Microsoft Word
- Experience working with individuals with disabilities
- Research
- Sick pay
Quick apply
9d
256100 R2 (LI) Senior Research Nurse
NHS Scotland —Edinburgh
- £43,231 - £52,679 a year
10d
R & D Scientist (Haematology)
AliveDx —Penicuik
- Full-time
- Data analysis skills
- Laboratory experience
- No degree
257754 (LC) Senior Research Nurse
NHS Scotland —Edinburgh
- £43,231 - £52,679 a year
- Part-time
- Nursing
- Travel
- Communication skills
1d
Advocacy Worker (18-Month Contract)
Partners in Advocacy —Leith
- Temporary
- Microsoft Word
- Experience working with individuals with disabilities
- Research
10d
Project Leader
Eurofins UK Product Testing Services —Edinburgh
- Full-time
- Computer literacy
- Computer skills
- Training & development
- Free parking
- Annual leave
Quick apply
13d
QC Stability Analyst
NextPharma —Livingston
- Full-time
- Microsoft Word
- Computer literacy
- Quality control
- Free parking
- Health & wellbeing programme
Quick apply
10d
Manager, Process Excellence
Catalent —Bathgate
- Full-time
- Engineering
- Analysis skills
- Bachelor's degree
- Free parking
- Employee assistance programme
Specialist Quality Control
NextPharma GmbH —Livingston
- Full-time
- Microsoft Word
- Computer literacy
- Quality control
- Life insurance
10d
Senior Advanced Nurse Practitioner
NHS Scotland —Kirkcaldy
- £65,125 - £70,303 a year
- Weekend availability
- Management
- Hospital
- Master's degree
7d
QC Technician- Days
Piramal Pharma Solutions Inc. —Grangemouth
- Bachelor's degree
- Continuous improvement
- Quality control
13d
Financial Accountant
Charles River Laboratories —Tranent
- £35,000 - £45,000 a year
- Full-time
- Hybrid work
- Bachelor's degree
- Accounting
- Communication skills
9d
Senior Financial Accountant
Charles River Laboratories —Tranent
- £45,000 - £55,000 a year
- Full-time
- Hybrid work
- Bachelor's degree
- Mentoring
- Accounting
9d
Trainee Dental Nurse
Scottish Orthodontics —Kirkcaldy
- £12.71 an hour
- Full-time
- CAD
- Bachelor's degree
- In-person
Quick apply
3d

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clinical study manager jobs near edinburgh, edh

Freelance Site Activation Specialist (Study Start-Up / Regulatory Submissions) – UK Remote

IQVIA -
Edinburgh

Apply Now

Job details

Full-time
2 days ago

Benefits

Work from home

Qualifications

Clinical research
Stakeholder collaboration
English
Bachelor's degree
Project schedule tracking
Multidisciplinary collaboration
Good Clinical Practice (GCP)
Communication skills
Good Clinical Practice (ICH-GCP) guidelines
Project progress tracking
Progress tracking

Full job description

Edinburgh, United Kingdom | Full time | Home-based | R1565336

Location: United Kingdom (Home-Based)
Contract Type: Freelance
FTE: 1.0
Start: Immediate
Duration: Approximately 3–6 months

About the Role

We are seeking an experienced Freelance Site Activation Specialist based in the United Kingdom to support clinical trial start-up and site activation activities.

The primary focus of this role will be UK submission document collection and preparation, site document review, Informed Consent Form (ICF) adaptations, and regulatory submission support. The successful candidate will work closely with investigative sites and internal study teams to ensure submission packages are complete, compliant, and delivered according to project timelines.

Key Responsibilities

Collect, review, and prepare site and regulatory documentation required for UK clinical trial submissions
Support the preparation and submission of regulatory packages in accordance with study requirements and local regulations
Perform and coordinate Informed Consent Form (ICF) adaptations and associated document updates
Review essential site documentation to support Regulatory Green Light readiness
Liaise directly with investigative sites to obtain, track, and resolve outstanding documentation
Ensure the completeness, accuracy, and quality of submission packages
Maintain study tracking systems, timelines, and submission records
Support site activation activities and monitor progress against project milestones
Collaborate closely with Site Activation Managers, Regulatory Affairs, Project Management, and other cross-functional teams
Ensure compliance with ICH-GCP, local UK regulations, and study-specific requirements

Requirements

Based in the United Kingdom
Minimum 2–3 years of experience in Site Activation, Study Start-Up, Regulatory Affairs, or Clinical Research
Strong experience with site document collection, review, and submission preparation
Experience supporting clinical trial regulatory submissions in the UK
Experience performing ICF adaptations
Solid understanding of site activation and study start-up processes
Strong attention to detail and ability to manage multiple priorities and timelines
Bachelor's degree in Life Sciences or a related field
Fluent English communication skills, both written and verbal

If this role sounds of interest, please apply today!

#LI-DNP

#LI-CES

#LI-HCPN

#LI-XS

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

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

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

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clinical study manager jobs in edinburgh, edh

Freelance Site Activation Specialist (Study Start-Up / Regulatory Submissions) – UK Remote

Product Development Scientist

Clinical Data Manager - FSP (Homebased - UK)

Advocacy Worker

256100 R2 (LI) Senior Research Nurse

R & D Scientist (Haematology)

257754 (LC) Senior Research Nurse

Advocacy Worker (18-Month Contract)

Project Leader

QC Stability Analyst

Manager, Process Excellence

Specialist Quality Control

Senior Advanced Nurse Practitioner

QC Technician- Days

Financial Accountant

Senior Financial Accountant

Trainee Dental Nurse

More jobs to discover

I want to receive the latest job alerts for clinical study manager in edinburgh, edh

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Location: United Kingdom (Home-Based)
Contract Type: Freelance
FTE: 1.0
Start: Immediate
Duration: Approximately 3–6 months

About the Role

Key Responsibilities

Requirements

Where you'll work

Home-based

Culture

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clinical study manager jobs in edinburgh, edh

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I want to receive the latest job alerts for clinical study manager in edinburgh, edh

Explore jobs in more locations

Location: United Kingdom (Home-Based) Contract Type: Freelance FTE: 1.0 Start: Immediate Duration: Approximately 3–6 months

About the Role

Key Responsibilities

Requirements

Where you'll work

Home-based

Culture

Location: United Kingdom (Home-Based)
Contract Type: Freelance
FTE: 1.0
Start: Immediate
Duration: Approximately 3–6 months