Clinical Trial Support & Data Entry Specialist

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

Job summary

IQVIA in Lakewood, CO is seeking a Full-time Clinical Research Aide to assist in conducting clinical trial activities in compliance with regulations. You will leverage strong organizational and collaborative skills to support study teams.

Responsibilities include screening and enrollment support, patient scheduling, data entry, and coordination of visits and laboratory procedures while adhering to protocols. This role offers growth within a global life sciences leader.

Qualifications

• Strong interpersonal and team-building abilities
• Ability to prioritize in changing conditions
• Excellent scheduling and coordination skills
• Attention to detail and data management

Responsibilities

• Screening, recruiting and enrollment of research subjects
• Scheduling patient/research visits
• Data entry and management
• Coordinate follow-up care and laboratory procedures
• Adhere to an IRB-approved protocol
• Assist in informed consent process
• Support safety of research subjects
• Coordinate protocol-related procedures

Skills

Interpersonal skills

Prioritization

Teamwork

Scheduling

Education

High School Diploma or equivalent

Bachelor's Degree

Job description

IQVIA in Lakewood, CO is seeking a Full-time Clinical Research Aide to assist in conducting clinical trial activities in compliance with regulations. You will leverage strong organizational and collaborative skills to support study teams.

Responsibilities include screening and enrollment support, patient scheduling, data entry, and coordination of visits and laboratory procedures while adhering to protocols. This role offers growth within a global life sciences leader.