Clinical Trials Research Assistant

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

Job summary

IQVIA is a leading global provider of clinical research services, supporting trials across life sciences and healthcare. The role focuses on assisting in the conduct of clinical trial activities in compliance with regulations, emphasizing communication, prioritization, and adaptability.

The position involves scheduling visits, collecting participant histories, coordinating procedures, and maintaining data integrity while supporting IRB protocols and safety measures for research subjects.

Qualifications

• Must have effective communication with study team members.
• Ability to screen, recruit and enroll research subjects.
• Data entry and management skills.
• Adhere to IRB approved protocol and informed consent process.

Responsibilities

• Develop strong working relationships with study team members.
• Build relationships with investigators and staff to foster trust between clinic and research office.
• Assist with screening, recruitment and enrollment of subjects.
• Perform scheduling of patients/research participants.
• Collect participant history and data.
• Coordinate follow-up care and laboratory procedures.
• Ensure compliance with SOPs and guidelines.
• Schedule subject visits and procedures.

Skills

Logical thinking

Prioritization

Adaptability

Interpersonal skills

Team building

Education

High School Diploma

Bachelors Degree

Job description

IQVIA is a leading global provider of clinical research services, supporting trials across life sciences and healthcare. The role focuses on assisting in the conduct of clinical trial activities in compliance with regulations, emphasizing communication, prioritization, and adaptability.

The position involves scheduling visits, collecting participant histories, coordinating procedures, and maintaining data integrity while supporting IRB protocols and safety measures for research subjects.