IQVIA

Healthcare

RegionalSpecialist

£35–45k ~AI est. Reading, Berkshire, United Kingdom FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“Regional Specialist at IQVIA. Skills: Remote clinical visits, Investigator site support, Clinician training. Support investigator sites onboarding. Train and onboard research clinicians”

What You'll Achieve.

Ensure remote visits are coordinated efficiently; Ensure remote visits are coordinated compliantly; Ensure remote visits are coordinated on time; Contribute to high levels of site satisfaction; Contribute to high levels of customer satisfaction

Industry & Context.

Healthcare
Problems you'll solve

Problem-solving

What They're Looking For.

Must Have

Bachelor's degree, 2 years of experience, Understanding of clinical trial conduct, Understanding of GCP principles, Proficiency with Microsoft Office

Nice to Have

Life Sciences or related field degree

What You'll Do.

Support investigator sites onboarding

Train and onboard research clinicians

Coordinate remote visit scheduling

Manage visit documentation

Perform quality checks

Follow up on corrections

Deliver study-specific training

Support compliance with GCP

Support compliance with regulatory requirements

Act as point of contact

Support courier bookings

How You'll Work.

Team & Collaboration

Investigator sites; Research clinicians; Internal teams; Global Lead; Study teams

Full Job Description

The Regional Specialist (RS) plays a key role in supporting remote clinical visits across global studies. This role works closely with investigator sites, research clinicians, and internal teams to ensure remote visits are coordinated efficiently, compliantly, and on time. Working in partnership with the Global Lead, the Regional Specialist helps manage visit delivery, supports study timelines, and contributes to high levels of site and customer satisfaction. **What you’ll do** * Support investigator sites onboarding into RNPS remote visit services * Train and onboard research clinicians to ensure study readiness * Coordinate remote visit scheduling, clinician assignments, and logistics * Manage visit documentation, trackers, and system access * Perform quality checks on study documentation and follow up on corrections * Deliver study‑specific training and support compliance with GCP and regulatory requirements * Act as a key point of contact for sites, clinicians, and internal study teams * Support courier bookings, shipment tracking, and supply coordination **What you’ll bring** * Bachelor’s degree in Life Sciences or a related field * At least 2 years of experience in clinical research, visit coordination, or project support * Understanding of clinical trial conduct and GCP principles * Strong communication, organization, and problem‑solving skills * Ability to manage multiple priorities in a global environment * Confidence working across teams, countries, and cultures * Proficiency with Microsoft Office applications IQVIA is a global leader in advancing clinical research and healthcare outcomes. Joining our team means contributing to impactful work while developing your career in a collaborative, international environment. 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 commercializa

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