Freelance Clinical Research Associate — UK Trials + Visa Sponsorship

Naija UK Connect; Greater London; Hybrid; GBP 34,000 - 55,000; Part time

Benefits offered by this job

Visa sponsorship available

Flexible freelance contract (0.5-0.7 F

Travel across the UK

Job summary

IQVIA Limited in the United Kingdom is seeking a Freelance Clinical Research Associate (CRA) to support Phase I–IV trials across the UK. The role involves a dynamic schedule with travel to multiple site visits to ensure trial integrity and progress.

You will oversee site evaluations, initiation, interim monitoring, and close-out visits, ensuring adherence to protocols and regulatory requirements, while collaborating with site staff and global teams.

Qualifications

• 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.

Responsibilities

• Oversee clinical investigations from start to finish, including site evaluation, initiation, interim monitoring, and close-out visits.
• Ensure all trial activities adhere to established protocols and regulatory guidelines.
• Travel across the UK to monitor and support trial sites.
• Collaborate with site staff and global teams to ensure trial integrity and progress.

Skills

Site interaction

Travel readiness

Clinical trial knowledge

Excellent communication

Job description

IQVIA Limited in the United Kingdom is seeking a Freelance Clinical Research Associate (CRA) to support Phase I–IV trials across the UK. The role involves a dynamic schedule with travel to multiple site visits to ensure trial integrity and progress.

You will oversee site evaluations, initiation, interim monitoring, and close-out visits, ensuring adherence to protocols and regulatory requirements, while collaborating with site staff and global teams.