At a Glance
- Tasks: Manage and oversee clinical trials across the UK, ensuring compliance and success.
- Company: Join IQVIA, a leading global healthcare intelligence company with a collaborative culture.
- Benefits: Flexible freelance contract, professional development, and explicit visa sponsorship for eligible applicants.
- Other info: Ideal for Nigerian and African immigrants seeking to leverage their expertise in the UK.
- Why this job: Make a real impact in clinical research while enjoying work-life balance and travel opportunities.
- Qualifications: Experience in Phase I-IV trials and strong communication skills required.
The predicted salary is between 36900 - 45100 £ per year.
Licensed visa sponsor
IQVIA Limited is on the Home Office register of licensed worker sponsors (Skilled Worker, Global
Business
Mobility: Senior or Specialist Worker), so it can sponsor a work visa.
This particular advert does not mention sponsorship, so confirm with the employer before you apply.
Applicants from Nigeria and elsewhere, in the UK or overseas, may apply.
Check any employer on our sponsor list
IQVIA is actively seeking Freelance CRAs across the UK, with positions available for those based in London.
This opportunity is ideal for Nigerian and African immigrants seeking to leverage their clinical research expertise in the UK, as visa sponsorship is explicitly available for foreign applicants.
While the salary isn't specified, the role offers a flexible 0.5 - 0.7 FTE freelance contract with an approximate 1-year duration.
Job Description
As a Freelance Clinical Research Associate (CRA) with IQVIA, you will play a crucial role in the preparation and execution of Phase I-IV clinical trials.
This involves a dynamic schedule, requiring travel across the UK for various site visits to ensure trial integrity and progress.
Your responsibilities will encompass overseeing clinical investigations from start to finish, including conducting site evaluation, initiation, interim monitoring, and close-out visits.
You will be instrumental in ensuring that all trial activities adhere to established protocols and regulatory guidelines, contributing significantly to the success of diverse clinical research projects.
Requirements
- Proven experience in Phase I-IV clinical trials.
- Ability to conduct site evaluation, initiation, and interim close-out visits.
- Strong understanding of clinical trial processes and regulatory requirements.
- Excellent communication and interpersonal skills for effective site interaction.
- Flexibility to travel extensively across the UK for site visits.
Right to work in the UK or eligibility for Skilled Worker (Tier 2) visa sponsorship is required.
Benefits
- Opportunity to work with a leading global healthcare intelligence company.
- Flexible freelance contract (0.5 - 0.7 FTE) allowing for work-life balance.
- Exposure to a wide range of Phase I-IV clinical trials.
- Professional development and networking opportunities within the UK clinical research sector.
- Explicit visa sponsorship available for eligible overseas applicants.
- How to Prepare
For Nigerian and African immigrants targeting a Freelance CRA role in the UK, it's vital to present your qualifications in a format familiar to UK employers.
Ensure your CV clearly highlights your clinical trial experience, specifying the phases you’ve worked on and your monitoring responsibilities.
Tailor your Linked In profile to reflect UK industry standards, showcasing your expertise and professional network.
When preparing for interviews, be ready to discuss your experience with UK-specific regulations if applicable, or demonstrate your adaptability to new regulatory environments.
Confidently address your visa sponsorship needs early in the process, as IQVIA has indicated its availability.
Practice articulating how your international experience directly translates to the demands of a UK-based CRA role.
- Ensure your CV is in a UK-optimised format, detailing clinical trial phases and monitoring duties.
- Update your Linked In profile to showcase relevant skills and experience for UK clinical research.
- Prepare a cover letter that clearly states your interest and acknowledges your need for visa sponsorship.
- Research common interview questions for CRAs and practice situational responses, particularly regarding regulatory compliance.
- Be prepared to discuss your existing professional registrations or certifications and how they align with UK standards.
- Visa Sponsorship & Foreigner Eligibility
Visa / Skilled Worker (Tier 2) sponsorship is explicitly available for this Freelance CRA role with IQVIA.
This means that foreigners, including non-UK residents and overseas applicants, are encouraged to apply if they require a UK work visa.
If your current visa status is borderline or you have unique circumstances, it is highly recommended to clearly state your situation in your application and cover letter to ensure it is properly reviewed.
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