Clinical Research Associate 2

🔥 0 minutes ago

🇪🇸 Spain – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🚫👨‍🎓 No degree required

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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IQVIA

WebsiteLinkedInAll Job Openings

10,000+ employees

💼 Consulting

🏭 Manufacturing

📣 Marketing

💰 $1G Post-IPO Debt on 2023-05

Consulting • Manufacturing • Marketing

IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.

📋 Description

• Perform site monitoring visits, including selection, initiation, monitoring, and close-out visits • Drive and track subject recruitment plans with study sites • Administer protocol and study training to assigned sites • Establish regular communication with sites to manage project expectations and issues • Evaluate site practices for protocol quality, integrity, and regulatory adherence • Escalate quality issues as appropriate • Track regulatory submissions, approvals, recruitment, enrollment, CRF completion, and data queries • Support the study start-up phase when applicable • Ensure site documents are available for Trial Master File filing • Verify Investigator's Site File maintenance according to GCP and local requirements • Maintain site management and monitoring documentation, visit reports, follow-up letters, and study documents • Collaborate with study team members to support project execution • Support development of site-level subject recruitment plans when applicable • Support site financial management and invoice retrieval when applicable

🎯 Requirements

• 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 • Knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines • Ability to perform site monitoring visits and manage clinical study documentation • All application information and credentials must be truthful and complete

🏖️ Benefits

• Collaborative culture • Home-based work in Spain • Opportunity to work across multiple therapeutic areas • Diversity, inclusion, and belonging culture