Clinical Research Coordinator - Sioux Falls, SD
About The Position
Clinical Research Coordinator – Sioux Falls, SD 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 innovation. This hands-on position combines clinical procedures, recruitment activities, and compliance to ensure the highest standards of care. About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We partner with top pharmaceutical, biotechnology, and medical device companies to accelerate innovation and improve lives. Our team blends scientific expertise with cutting-edge technology to deliver insights that transform clinical trials and healthcare worldwide. What You’ll Do Perform complex clinical procedures, including ECG, spirometry, sample collection, and vital signs Phlebotomy required Coordinate clinical research studies and ensure compliance with protocols and Good Clinical Practice (GCP) Prepare study materials, set up equipment, and manage logistical activities Recruit, screen, and orient volunteers while prioritizing their safety and well-being Collect and accurately record clinical data in case report forms (CRFs) Collaborate with investigators and monitors to resolve queries and maintain data quality Act as a volunteer advocate and maintain a safe environment in line with Health and Safety policies Focus on Recruitment and Pre-ICF Activities: Pre-screening & recruitment support including chart reviews, referral management, and community outreach Make eCRF entries, corrections, and queries Investigator Site File maintenance Regulatory experience would be a plus
Requirements
- High School Diploma or equivalent education and 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
- Advanced-level experience supporting site lead CRC with patient visits, data entry/query resolution, and prescreening physician referrals for eligibility
- Experience working in both research and clinical settings
- Please note: This position is not eligible for sponsorship.
Nice To Haves
- Regulatory experience would be a plus
Responsibilities
- Perform complex clinical procedures, including ECG, spirometry, sample collection, and vital signs
- Phlebotomy required
- Coordinate clinical research studies and ensure compliance with protocols and Good Clinical Practice (GCP)
- Prepare study materials, set up equipment, and manage logistical activities
- Recruit, screen, and orient volunteers while prioritizing their safety and well-being
- Collect and accurately record clinical data in case report forms (CRFs)
- Collaborate with investigators and monitors to resolve queries and maintain data quality
- Act as a volunteer advocate and maintain a safe environment in line with Health and Safety policies
- Focus on Recruitment and Pre-ICF Activities: Pre-screening & recruitment support including chart reviews, referral management, and community outreach
- Make eCRF entries, corrections, and queries
- Investigator Site File maintenance
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What This Job Offers
Job Type
Part-time
Career Level
Entry Level
Education Level
High school or GED
Number of Employees
5,001-10,000 employees
