New · posted Nov 4
IQVIA · Pharmaceuticals
Clinical Research Coordinator
- Wyomissing, PA
- On-site
- Part-time
- Associate & Specialist
The role
We are seeking a Clinical Research Coordinator (CRC) to join our team and support clinical research studies under the supervision of a principal investigator. This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance.
Clinical Research Coordinator - Wyomissing, PA
Work Set-Up: On-site Schedule Weekly Hours: 24 hours/week
What you need
- Bachelor’s degree preferred or equivalent combination of education and relevant experience.
- Minimum 1+ years of relevant work experience in clinical research.
- Working knowledge of clinical trials, GCP principles, and medical terminology.
- Strong attention to detail and ability to establish effective working relationships.
- Proficiency with EDC systems, data entry accuracy, and query management.
Please note: This position is not eligible for sponsorship.
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.
The potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
What you'll do
- Perform a variety of clinical procedures, including ECG, sample collection, and vital signs.
- Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines.
- Support study conduct by preparing study materials, setting up equipment, and planning logistical activities.
- Recruit, screen, and orient patients, ensuring their safety and well-being throughout the study.
- Collect and accurately record clinical data in case report forms (CRFs).
- Collaborate with investigators and monitors, addressing queries and ensuring data quality.
- Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.
Pay
$72,800 – $87,360 a year
Employer provided$35.00 – $42.00 an hour · yearly at 2,080 hours (40 a week)
How this comparesWhere you'll work
Wyomissing, PAOn-siteOpen in Maps (opens in a new tab)
More jobs in Wyomissing, PA
From the posting
About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.
Equal opportunity, accessibility and legal noticesIQVIA's statements, word for word
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
Job intelligence
The context around this role
Live data · November 4, 2026
Salary intelligence
How the pay compares
This role's midpoint is 22% below the US median for Clinical Research roles at this level.
This roleEmployer provided
Associate & Specialist roles in Pennsylvania7 roles publishing pay
Associate & Specialist roles in the US66 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $72,800 | — | $87,360 |
| Pennsylvania (middle half) | $102,500 | $102,500 | $102,500 |
| All US (middle half) | $92,750 | $102,500 | $125,000 |
This role: IQVIA's own published range, converted to a year at 2,080 hours. Comparisons: the base pay employers published on open Clinical Research roles at the same level on Regulatory Jobs, November 4, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Research
The general path across 216 open Clinical Research roles on Regulatory Jobs, with the titles they carry most. Not IQVIA's own promotion track.
Career resources on Clinical Research
Skills DNA
What this role leans on
How many of the posting's 18 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Clinical trial conduct7
- GMP and compliance3
- Documentation and SOPs3
- Investigations and CAPA2
- Collaboration and leadership2
- Lab testing and methods1
- Validation and qualification1
- Data and digital systems1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Clinical Research work in pharmaceuticals, led by the one this posting names, each linked to the agency or standards body that publishes it.
- ICHICH E6(R3) good clinical practice(official source, opens in a new tab)The international standard for the design, conduct and reporting of clinical trialsNamed in the posting
- FDA21 CFR Part 312(official source, opens in a new tab)Investigational New Drug applications and sponsor duties in drug trials
- FDA21 CFR Part 50(official source, opens in a new tab)Protection of human subjects: informed consent in FDA-regulated trials
- FDA21 CFR Part 56(official source, opens in a new tab)Institutional review boards for FDA-regulated clinical investigations
- EUEU Clinical Trials Regulation 536/2014(official source, opens in a new tab)How clinical trials of medicines are authorized and run in the EU, through CTIS
- ICHICH E8(R1)(official source, opens in a new tab)General considerations for clinical studies and quality by design in trials
- HHS45 CFR Part 46 (Common Rule)(official source, opens in a new tab)The federal policy for the protection of human research subjects
- NIH42 CFR Part 11(official source, opens in a new tab)Clinical trial registration and results reporting on ClinicalTrials.gov
- FDAFDA Bioresearch Monitoring (BIMO)(official source, opens in a new tab)FDA inspections of clinical investigators, sponsors, IRBs and GLP labs
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- HHSHIPAA Privacy Rule(official source, opens in a new tab)Federal protections for individually identifiable health information
- EUGDPR (Regulation 2016/679)(official source, opens in a new tab)The EU General Data Protection Regulation for personal data, including health data
- ICHICH E9 and E9(R1)(official source, opens in a new tab)Statistical principles for clinical trials and estimands
- FDA21 CFR 314.80 and 600.80(official source, opens in a new tab)Postmarketing reporting of adverse drug and biologic experiences
- ICHICH E2A to E2F(official source, opens in a new tab)Clinical safety data management, expedited reporting and periodic safety reports
- ICHMedDRA(official source, opens in a new tab)The ICH medical terminology for coding adverse events and medical history
Company hiring pulse
IQVIA on Regulatory Jobs
- 85
- Open roles
- 59
- Distinct roles
- 28
- Locations
By discipline
- Clinical74 87%
- Regulatory7 8%
- Quality4 5%
By level
- Associate & Specialist45 53%
- Manager15 18%
- Senior & Principal15 18%
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Clinical Research Coordinator at IQVIA
Open until filled. $73K–$87K a year, employer provided.