IQVIA
Clinical Research Coordinator – Surprise, AZ
Work Setup:
On-site Schedule:
Part-time (24 hours per week) Shape the Future of Medicine with IQVIA!
Are you passionate about advancing healthcare and improving patient outcomes? Join IQVIA as a
Clinical Research Coordinator (CRC)
and play a vital role in supporting clinical research studies that drive meaningful innovation. This hands‑on role blends clinical procedures, patient recruitment, and study compliance to ensure the highest standards of safety and care. About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We partner with leading pharmaceutical, biotechnology, and medical device organizations to accelerate innovation and improve patient lives. Our teams combine scientific expertise with advanced technology to transform clinical trials and healthcare delivery. What You’ll Do
Perform complex clinical procedures including ECG, spirometry, sample collection, phlebotomy, and vital signs Coordinate clinical research studies while ensuring adherence to study protocols and Good Clinical Practice (GCP) Prepare study materials, manage logistics, and support overall site operations Recruit, pre‑screen, and orient volunteers, including chart reviews, physician referrals, and community outreach Communicate study details effectively to potential participants and assess patient eligibility based on inclusion/exclusion criteria Collect, verify, and accurately document clinical data in case report forms (CRFs) and electronic CRFs (eCRFs), including corrections and query resolution Assist with Investigator Site File maintenance and collaborate with investigators and monitors to resolve study‑related issues Maintain a safe environment for volunteers in alignment with Health & Safety policies What We’re Looking For
High School Diploma or equivalent education/experience Minimum 1 year of relevant clinical research experience (preferred) Working knowledge of clinical trials, GCP principles, and medical terminology Strong attention to detail and ability to build effective working relationships Experience supporting lead CRCs with patient visits, data entry, query resolution, and prescreening referrals Experience in both research and clinical settings Experience with patient recruitment and prescreening, strong communication skills to discuss study details with patients, familiarity with trial activities from start‑up to close‑out, and clinical knowledge to interpret inclusion/exclusion criteria Regulatory experience is a plus 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 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. 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.
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Work Setup:
On-site Schedule:
Part-time (24 hours per week) Shape the Future of Medicine with IQVIA!
Are you passionate about advancing healthcare and improving patient outcomes? Join IQVIA as a
Clinical Research Coordinator (CRC)
and play a vital role in supporting clinical research studies that drive meaningful innovation. This hands‑on role blends clinical procedures, patient recruitment, and study compliance to ensure the highest standards of safety and care. About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We partner with leading pharmaceutical, biotechnology, and medical device organizations to accelerate innovation and improve patient lives. Our teams combine scientific expertise with advanced technology to transform clinical trials and healthcare delivery. What You’ll Do
Perform complex clinical procedures including ECG, spirometry, sample collection, phlebotomy, and vital signs Coordinate clinical research studies while ensuring adherence to study protocols and Good Clinical Practice (GCP) Prepare study materials, manage logistics, and support overall site operations Recruit, pre‑screen, and orient volunteers, including chart reviews, physician referrals, and community outreach Communicate study details effectively to potential participants and assess patient eligibility based on inclusion/exclusion criteria Collect, verify, and accurately document clinical data in case report forms (CRFs) and electronic CRFs (eCRFs), including corrections and query resolution Assist with Investigator Site File maintenance and collaborate with investigators and monitors to resolve study‑related issues Maintain a safe environment for volunteers in alignment with Health & Safety policies What We’re Looking For
High School Diploma or equivalent education/experience Minimum 1 year of relevant clinical research experience (preferred) Working knowledge of clinical trials, GCP principles, and medical terminology Strong attention to detail and ability to build effective working relationships Experience supporting lead CRCs with patient visits, data entry, query resolution, and prescreening referrals Experience in both research and clinical settings Experience with patient recruitment and prescreening, strong communication skills to discuss study details with patients, familiarity with trial activities from start‑up to close‑out, and clinical knowledge to interpret inclusion/exclusion criteria Regulatory experience is a plus 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 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. 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.
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