Clinical Research Associate 2

IQVIA

Clinical Research Associate role monitoring clinical studies for biotech firms. Perform compliance checks and manage project timelines while based in Spain.

Posted 7/2/2026full-timeRemote • 🇪🇸 SpainJuniorMid-LevelWebsite

About the role

Key responsibilities & impact

Perform site monitoring visits in accordance with contracted scope of work and regulatory requirements
Work with sites to adapt, drive, and track subject recruitment plan
Administer protocol and related study training to assigned sites
Evaluate the quality and integrity of study site practices
Manage the progress of assigned studies by tracking regulatory submissions and approvals
Ensure copies/originals site documents are available for filing in the Trial Master File (TMF)
Create and maintain appropriate documentation regarding site management
Collaborate and liaise with study team members for project execution support

Requirements

What you’ll need

Bachelor's Degree in scientific discipline or health care preferred
Requires at least 1.5 years of on-site monitoring experience
Equivalent combination of education, training and experience may be accepted
Organizational, time management and problem-solving skills
Ability to establish and maintain effective working relationships with coworkers, managers, and clients
Flexibility to travel
Driver’s license

Benefits

Comp & perks

Professional development opportunities
Flexible work arrangements

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools

Site MonitoringRegulatory ComplianceStudy ManagementDocumentation ManagementSubject Recruitment Planning

Soft Skills

Organizational SkillsTime ManagementProblem-Solving SkillsInterpersonal SkillsFlexibility

Certifications

Bachelor's Degree