Hunter Starr
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Hunter Starr Email & Phone Number

Clinical Research Associate II at ICON plc
Location: Raleigh, North Carolina, United States 8 work roles 2 schools
1 work email found @iqvia.com LinkedIn matched
✓ Verified August 2026 4 data sources Profile completeness 86%

Contact Signals · 1 work email

Work email h****@iqvia.com
LinkedIn Profile matched
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Current company
Role
Clinical Research Associate II
Location
Raleigh, North Carolina, United States
Company size

Who is Hunter Starr? Overview

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Quick answer

Hunter Starr is listed as Clinical Research Associate II at ICON plc, a with 52333 employees, based in Raleigh, North Carolina, United States. AeroLeads shows a work email signal at iqvia.com and a matched LinkedIn profile for Hunter Starr.

Hunter Starr previously worked as Clinical Research Associate at Iqvia and Senior Clinical Trials Assistant at Iqvia. Hunter Starr holds Master Of Public Health - Mph, Epidemiology, 3.6 from The Brody School Of Medicine At East Carolina University.

Company email context

Email format at ICON plc

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{first}.{last}@iqvia.com
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Profile bio

About Hunter Starr

Hunter Starr is a Clinical Research Associate II at ICON plc.

Current workplace

Hunter Starr's current company

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ICON plc
Icon Plc
Clinical Research Associate II
Raleigh, NC, US
Website
Employees
52333
AeroLeads page
8 roles

Hunter Starr work experience

A career timeline built from the work history available for this profile.

Clinical Research Associate Ii

Raleigh, Nc, Us

Clinical Research Associate

Durham, North Carolina, United States

• Perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice.• If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.• Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.• Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas.• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.• Build awareness of features and opportunities of study to site.• Collaborate and liaise with study team members for project execution support as appropriate.

Senior Clinical Trials Assistant

Durham, North Carolina, United States

• Assisted Clinical Team Lead (CTL) and Clinical Research Associates (CRAs) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.• Collaborated with CTL on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assisted with periodic review of study files for accuracy and completeness.• Collaborated with CTL on the preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.• Assisted with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.• Acted as a central contact for the clinical team for designated project communications, correspondence and associated documentation.• Assisted in training and orienting new staff. Acted as a mentor for less experienced CTAs.• Performed assigned administrative tasks to support team members with clinical trial execution.

May 2021 - Jan 2024

Pharmacy Technician

Clayton, North Carolina, United States

• Provided quality customer service by greeting each customer, assisting with questions and issues in person and on the phone while maintaining patient confidentiality• Retrieving, counting, and measuring drugs (except narcotics) and capping/uncapping vials and bottles• Maintained inventory levels and pulling outdated/recalled merchandise• Referring all doctor’s calls and customer’s medical questions to the pharmacist

Jul 2017 - Mar 2022

Graduate Assistant/Assistant Program Coordinator

Ecu Adult Specialty Care Clinic

Greenville, North Carolina Area

• Assisted on projects related to Clostridium difficile infection, bone density in HIV positive patients, Mino-Lok, and MyChart• Maintained inventory levels and pulling outdated merchandise• Scheduled package pickup of laboratory samples of patients• Filed paperwork and invoices for multiple studies including information containing patient and correspondence• Reviewed patients weekly for eligibility in SERES study • Conducted research related to the establishment of antibiotic protocols, reduction to antibiotic-resistant infections, and bone density in HIV positive patients• Created source documents

Jan 2018 - Apr 2019

Graduate Assistant

Greenville, North Carolina Area

• Engaged in literature searches• Updated citations bibliography for manuscripts using EndNote• Handled administrative tasks including preparation of materials for meetings

Sep 2017 - Dec 2017

Volunteer Intern

Metrolina Healthcare Preparedness Coalition

Charlotte, North Carolina Area

• Supervised events sponsored by MHPC• Updated brochure for State Medical Assistance Team requirement• Researched Zika virus on potential long-term impacts on emergency healthcare• Presented Zika virus information and initiated discussions with professionals on strategies to reduce Zika impact• Designed and created a poster on results of Zika research and discussion

Jun 2016 - Aug 2016
Team & coworkers

Colleagues at ICON plc

Other employees you can reach at iqvia.com. View company contacts for 52333 employees →

2 education records

Hunter Starr education

Bachelor Of Science - Bs, Public Health, 3.6

Activities and Societies: Ultimate Frisbee: August 2013-August 2014 Running Club: August 2014-May 2017Minor: Communication

FAQ

Frequently asked questions about Hunter Starr

Quick answers generated from the profile data available on this page.

What company does Hunter Starr work for?

Hunter Starr works for ICON plc.

What is Hunter Starr's role at ICON plc?

Hunter Starr is listed as Clinical Research Associate II at ICON plc.

What is Hunter Starr's email address?

AeroLeads has found 1 work email signal at @iqvia.com for Hunter Starr at ICON plc.

Where is Hunter Starr based?

Hunter Starr is based in Raleigh, North Carolina, United States while working with ICON plc.

What companies has Hunter Starr worked for?

Hunter Starr has worked for Icon Plc, Iqvia, Cvs Pharmacy, Medical Edge Recruitment, and Ecu Adult Specialty Care Clinic.

Who are Hunter Starr's colleagues at ICON plc?

Hunter Starr's colleagues at ICON plc include Patrick Nwanah, Ranjeetha Srinivas, Satoko Ogane, Tsveta Stranska, and Evelin Cassini.

How can I contact Hunter Starr?

You can use AeroLeads to view verified contact signals for Hunter Starr at ICON plc, including work email, phone, and LinkedIn data when available.

What schools did Hunter Starr attend?

Hunter Starr holds Master Of Public Health - Mph, Epidemiology, 3.6 from The Brody School Of Medicine At East Carolina University.

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