Regulatory affairs specialist Work, Jobs in Witney (with Salaries)

Freelance Site Activation Specialist (Study Start-Up / Regulatory Submissions) – UK Remote
IQVIA —Oxford
- Full-time
- Remote
- English
- Bachelor's degree
- Communication skills
- Work from home
3d
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Campden BRI —Chipping Campden
- Remote
- Business development
- Project management
- Continuous improvement
- Employee discount
Sensory Insights Manager
Campden BRI —Chipping Campden
- Doctoral degree
- Data analysis skills
- Business development
- Employee discount

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

IQVIA -
Oxford

Apply Now

Job details

Full-time
3 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

Oxford, 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.

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regulatory affairs specialist jobs in witney

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

Regulatory Innovation & Nutrition Manager

Sensory Insights Manager

More jobs to discover

I want to receive the latest job alerts for regulatory affairs specialist in witney

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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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regulatory affairs specialist jobs in witney

Regulatory Innovation & Nutrition Manager

Sensory Insights Manager

More jobs to discover

I want to receive the latest job alerts for regulatory affairs specialist in witney

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