IQVIA
Healthcare
RegionalSpecialist
Neural analysis suggests this role is
optimal for Mid+ candidates.
“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.
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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