Clinical Research Coordinator - Sioux Falls, SD

IQVIA; Sioux Falls (SD); On-site; USD 48,216 - 57,859; Part time

Job summary

IQVIA in Sioux Falls, SD is seeking a Clinical Research Coordinator for a part-time, on-site role. The successful candidate will perform complex clinical procedures and coordinate research studies while ensuring compliance with regulations.

The position requires a High School Diploma or equivalent and at least one year of relevant clinical research experience. Strong attention to detail and effective relationship-building skills are essential for success in this role.

The pay range for this role is $35.00-$42.00 per hour based on qualifications and experience.

Qualifications

• Minimum 1 year of relevant clinical research experience preferred.
• Advanced-level experience supporting site lead CRC with patient visits.
• Experience working in both research and clinical settings.

Responsibilities

• Perform complex clinical procedures including ECG and sample collection.
• Coordinate clinical research studies and ensure compliance with protocols.
• Recruit, screen, and orient volunteers while prioritizing their safety.

Skills

Attention to detail

Clinical research experience

Knowledge of GCP

Medical terminology

Education

High School Diploma or equivalent

Job description

Clinical Research Coordinator – Sioux Falls, SD

Work Setup: On-site

Schedule: Part-time (24 hours per week)

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

What We’re Looking For

• 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.

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.

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.

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.