As an Associate Principal of the DTAS (Data, technology and Advisory Services) Health Economics / Health Technology Assessment (HE/HTA) practice, you will work directly with life sciences clients as a…
€74.3k – €126.5k a yearLondon
UK jobs. Bigger possibilities.
136,000+ live jobsFreelance Site Activation Specialist
Remote, London·Full-time·Added 1 month ago (last checked 8 Oct)
Overview
Job details
Freelance role
Full-time.
Fully remote
Only from certain places, per the ad: “Based in the United Kingdom”
Requirements
Have 2+ years of experience
Mid-level role.
Skills
The role
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.
Hiring process
1 interview
- Other interviews are conducted on Microsoft Teams, unless otherwise specified.
- Most interviews are conducted in English unless otherwise specified. However, some questions may be asked in local language.
- The use of AI support during an interview or online assessment is strictly prohibited and grounds for disqualification.
About IQVIA
- Industry
- Clinical Research and Health Data
- Founded
- 1982
- Employees
- 50,000–100,000
- Headquarters
- Durham, USA
- Website
- iqvia.com
More jobs like this
or browse London·Healthcare·Mid-level·Remote·Biotech & Life Sciences·Clinical Research and Health Data
Clinical Monitoring Analyst (Cluepoints)
IQVIA5d ago
This unique role within IQVIA lends itself to a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) with strong communication and organisation skills.
Remote, London
Cloud FinOps Engineer
IQVIA5d ago
The Cloud FinOps Engineer is responsible for the financial governance, optimization, reporting, forecasting, and commercial management of the organization's public cloud estate across Azure, AWS, and…
London
Data Standards Engineer
IQVIA5d ago
This position is responsible for the development of the end-to-end design of client standards and study specifications that align to the CDISC standards and regulatory agency guidance's.
Reading
Epidemiologist
IQVIA5d ago
In this role, one must collaborate with global clients and cross-functional teams to provide epidemiology expertise for real-world evidence (RWE) studies across the full spectrum of study designs and…
London
PK/PD Statistical Programmer
IQVIA5d ago
We are seeking an experienced PK/PD Statistical Programmer with strong experience in R programming , PK/PD datasets , and NONMEM dataset creation .
Remote, Reading
Senior Medical Writer
IQVIA5d ago2 openings
The FTE Medical Writer will serve as an integrated member of the team, delivering medical writing services for the development of clinical documents, including Clinical Trial Reports (CTRs), Trial…
London
Instrument Licensing Solutions and Patient & Site Strategy helps organizations understand how patients feel and function in clinical research and routine care.
London
Associate Manager - Biochem
IQVIA1w ago
Responsible for supervising a team of lab staff and ensuring effective operational delivery and for setting day to day operational activities for the team with a focus on daily delivery.
West Lothian
Job Overview Manages multiple consulting projects of varying complexity and ensures on-time and on-budget delivery for clients in the healthcare field.
London
Clinical Pharmacist
IQVIA1w ago6 locations
Hybrid in London
Facilities Assistant
IQVIA1w ago
Manchester