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…
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136,000+ live jobsRegional Specialist
On-site in Reading·Full-time·Added 10 days ago (last checked 4 Oct)
Overview
Job details
Full-time
Per the ad.
Requirements
Work on-site in Reading
No relocation package mentioned.
Have 2+ years of experience
Junior-level role.
Skills
Requirements
What we're looking for
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
The role
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
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
In their own words
Additional information
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 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.
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