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Regional Specialist, Remote Research Services

Role overview

Qualifications

  • Bachelor's degree in Life Sciences or a related field
  • Experience in clinical research, clinical operations, study coordination, project management, or a related healthcare environment
  • Strong organizational skills with the ability to manage multiple priorities in a fast-paced environment
  • Excellent communication and relationship-building skills

Responsibilities

  • Become a trusted partner for investigator sites, clinicians, and study teams throughout the lifecycle of remote research activities
  • Lead site and clinician onboarding, ensuring teams are fully prepared and confident in delivering remote trial visits
  • Coordinate and oversee remote patient visits, ensuring seamless execution and an exceptional experience for sites and patients
  • Deliver study-specific training and ongoing support to research clinicians and site personnel

Key facts

Other skills

  • Training And Development
  • Microsoft Office
  • Communication
  • Relationship Building
  • Organizational Skills

About the company

IQVIA logo

IQVIA

Contract Research Organizations (CRO)

IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligenceβ„’ delivers powerful insights with speed and agility β€” enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 86,000 employees, IQVIA conducts operations in more than 100 countries. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific advances, in an effort to advance their path toward cures. To learn more, visit www.iqvia.com.

Company details

Company typeLarge
IndustryContract Research Organizations (CRO)
Company size10001

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Job description

Are you passionate about clinical research and enjoy working with people, projects, and innovative approaches to patient care?

As a Regional Specialist, you will play a key role in the delivery of remote clinical trial visits, helping bring research directly to patients. Working closely with investigator sites, healthcare professionals, and internal study teams, you will ensure the successful coordination and execution of remote research activities across multiple studies.

This is a highly collaborative role that combines clinical research knowledge, project coordination, stakeholder management, and operational excellence. You will have the opportunity to work with cross-functional teams around the globe while contributing to innovative patient-centric research solutions that improve access to clinical trials.

What You'll Do

  • Become a trusted partner for investigator sites, clinicians, and study teams throughout the lifecycle of remote research activities.
  • Lead site and clinician onboarding, ensuring teams are fully prepared and confident in delivering remote trial visits.
  • Coordinate and oversee remote patient visits, ensuring seamless execution and an exceptional experience for sites and patients.
  • Deliver study-specific training and ongoing support to research clinicians and site personnel.
  • Collaborate with internal and external stakeholders to resolve operational challenges and drive study success.
  • Ensure high standards of quality, compliance, and documentation in line with GCP, ICH, and company requirements.
  • Manage logistics, supplies, and courier activities to support uninterrupted study delivery.
  • Contribute to the growth and continuous improvement of innovative decentralized and remote research solutions.

What We're Looking For

  • Bachelor's degree in Life Sciences or a related field.
  • Experience in clinical research, clinical operations, study coordination, project management, or a related healthcare environment.
  • Strong organizational skills with the ability to manage multiple priorities in a fast-paced environment.
  • Excellent communication and relationship-building skills.
  • Passion for patient-focused clinical research and innovative care delivery models.
  • Knowledge of ICH-GCP and clinical trial processes is preferred.
  • Proficiency with Microsoft Office and other digital collaboration tools.

Why Join Us?

  • Be part of the future of clinical research through innovative remote and decentralized trial solutions.
  • Work in a highly collaborative, international environment.
  • Build expertise across clinical operations, stakeholder management, training, and project coordination.
  • Make a meaningful impact by helping improve patient access to clinical trials.
  • Gain broad exposure across multiple therapeutic areas and study programs.

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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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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