Clinical Research Associate 2

🕒 July 2

🇪🇸 Spain – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🚫👨‍🎓 No degree required

👻 Ghost score 40%

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 • Work with sites to adapt, drive, and track subject recruitment plans • Administer protocol and study training to assigned sites • Establish regular communication with sites to manage project expectations and issues • Evaluate study site practices for protocol quality, integrity, and regulatory adherence • Escalate quality issues as appropriate • Track regulatory submissions and approvals, recruitment and enrollment, CRF completion and submission, and data query generation and resolution • 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 regulatory requirements • Create and maintain site management documentation, monitoring visit findings, and action plans • Submit visit reports and generate follow-up letters and other required study documentation • Collaborate with study team members to support project execution • Support development of project subject recruitment plans on a per-site basis when applicable • Support site financial management and retrieve invoices according to clinical trial agreements and local requirements 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 and adherence to Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines • Ability to work across multiple therapeutics, including Oncology, Hematology, and Cardiovascular • Must be based in Spain

🏖️ Benefits

• Diversity, inclusion, and belonging culture • Opportunity to work with talented employees worldwide • Equal opportunities for women and men