Clinical Research Associate II – Hematology

🔥 1 minute ago

🇦🇷 Argentina – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 10%

What it means: the chance that no one is really hiring for this job.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

Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.

📋 Description

• Lead site qualification, initiation, monitoring, and closeout visits • Ensure adherence to study protocols, GCP, and regulatory requirements • Oversee site performance, data quality, and patient safety through monitoring, source document verification, and risk identification • Build relationships with investigative sites and provide training, guidance, and ongoing support • Coordinate and review study documentation, regulatory submissions, investigator site files, and Trial Master File updates • Partner with project teams to track study milestones, evaluate deliverables, and contribute to operational planning and execution • Serve as a Lead CRA on global studies • Coordinate monitoring activities and mentor and train less experienced CRAs • Facilitate resolution of data queries and review paper and electronic CRFs • Support timely and accurate study data collection • Contribute to study team meetings, investigator meetings, bid defenses, monitoring plans, study-specific tools, and training materials • Travel regionally to investigative sites, with occasional travel to other locations as needed

🎯 Requirements

• Medical Doctor (MD) degree or Pharmacy degree with at least 2 years of Clinical Research Associate experience; OR a four-year degree in a life science-related field with at least 3 years of CRA experience; OR a two-year college curriculum/equivalent training (nursing or life science preferred) with at least 4 years of CRA experience • Extensive knowledge of clinical research processes, GCP, ICH guidelines, FDA and/or regulations, and local regulatory requirements • Demonstrated experience independently managing site monitoring activities across the clinical trial lifecycle • Strong understanding of multiple therapeutic areas and ability to function as a Lead CRA • Proficiency with Microsoft Office, IxRS platforms, and electronic data capture (EDC) systems • Excellent communication, organization, time management, problem-solving, and relationship-building skills • Ability to mentor and influence others • Fluency in local language(s) required for assigned countries • Proficiency in spoken and written English • Must reside in Argentina • Ability to travel to investigative sites approximately 6–10 days per month

🏖️ Benefits

• Collaborative and inclusive environment • Growth and career development opportunities • Opportunity to learn and grow • Mentoring and training opportunities • Home-based/remote work arrangement

📊 Check your resume score for this job

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

Upload Resume