Clinical Research Associate II

🔥 0 minutes ago

🇪🇸 Spain – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 12%

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.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Linical

WebsiteLinkedInAll Job Openings

501 - 1000 employees

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

Linical is a global Clinical Research Organization (CRO) that partners with biopharmaceutical companies to manage and support clinical trials across various therapeutic areas such as oncology, neurology, psychiatry, immunology, and endocrinology. With extensive expertise in drug development strategy, protocol development, regulatory consulting, and patient recruitment, Linical guides clients through every phase of their clinical development journey. They emphasize quality data capture, personalized service, and overcoming obstacles to ensure successful clinical trials, helping to bring new therapies to patients worldwide. Linical's global reach and award-winning services make them a reliable partner for conducting complex clinical studies.

📋 Description

• Manage investigative sites across Spain • Conduct site qualification, initiation, monitoring, and close-out visits • Ensure patient safety, data integrity, and protocol compliance • Perform source data verification and review study documentation • Manage site relationships and provide ongoing support to investigators and study staff • Assist with ethics committee and regulatory submissions where required • Monitor investigational product accountability and site performance • Maintain Trial Master File (TMF) documentation and support query resolution • Collaborate with cross-functional study teams to ensure successful trial delivery

🎯 Requirements

• Life Sciences degree or equivalent experience • Recognized CRA training • Minimum 4 years' clinical research experience • Minimum 2 years' monitoring experience as a CRA • Strong knowledge of ICH-GCP, clinical trial regulations, and site management • Fluent in Spanish and English • Portuguese is desirable • Excellent communication, organisation, and problem-solving skills • Ability to work independently and manage multiple priorities • Valid driver's license • Willingness to travel up to 75%

🏖️ Benefits

• Home-based flexibility • Opportunity to work on international clinical trials • Collaborative and supportive team environment • Competitive salary and benefits package