Clinical Trials Research Coordinator

IQVIA; Lakewood (CO); On-site; USD 30,000 - 76,000; Full time

Job summary

IQVIA is seeking a dedicated professional to assist in conducting clinical trial activities in compliance with regulatory requirements. The role emphasizes logical thinking, prioritization, adaptability, and strong interpersonal skills to support the study team and investigators in a collaborative environment.

You will screen and recruit participants, schedule visits, manage data entry, and ensure adherence to study protocols while maintaining subject safety and workflow efficiency across the

Qualifications

• High School Diploma or equivalent Req
• Bachelor's Degree Pref

Responsibilities

• Develop strong working relationships and maintain effective communication with study team members
• Develop strong working relationships with the investigators and office staff to build a foundation of trust and respect between the clinic and the research office
• Assists with the screening, recruiting and enrollment of research subjects
• Perform patient/research participant scheduling
• Collect patient/research participant history
• Data entry and management
• Coordinate follow up care and laboratory procedures
• Adhere to an IRB approved protocol
• Assist in the informed consent process of research subjects
• Support the safety of research subjects
• Coordinate protocol related research procedures, study visits, and follow up care
• Comply with company and Sponsor policies, standard operating procedures (SOPs) and guidelines
• Schedule subject visits and procedures

Skills

Logical thinking

Prioritization

Adaptability

Interpersonal skills

Team building

Education

High School Diploma or equivalent

Bachelor's Degree Pref

Job description

IQVIA is seeking a dedicated professional to assist in conducting clinical trial activities in compliance with regulatory requirements. The role emphasizes logical thinking, prioritization, adaptability, and strong interpersonal skills to support the study team and investigators in a collaborative environment.

You will screen and recruit participants, schedule visits, manage data entry, and ensure adherence to study protocols while maintaining subject safety and workflow efficiency across the