Clinical Research Associate

🔥 1 hour ago

🇮🇱 Israel – 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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AbbVie

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 2013

🏥 Healthcare

💼 Consulting

🏭 Manufacturing

Healthcare • Consulting • Manufacturing

AbbVie is a global pharmaceutical company that discovers and delivers innovative medicines and solutions to enhance lives. With a focus on addressing the world's toughest health challenges, AbbVie operates in over 175 countries, providing a wide range of products across areas like immunology, oncology, neuroscience, and aesthetics. Committed to scientific innovation, AbbVie invests heavily in research and development, aiming to produce first-in-class medicines. The company also emphasizes workplace diversity, sustainability, and patient support initiatives, ensuring positive impact for both its patients and the broader community.

📋 Description

• Monitor activities conducted by clinical investigative sites in support of AbbVie clinical studies • Ensure adherence to federal and applicable local regulations, Good Clinical Practice (GCP), ICH Guidelines, AbbVie SOPs, monitoring plans, and quality standards • Conduct site qualification, initiation, interim monitoring, and study closeout visits for Phase 1–4 studies • Oversee site personnel activities and motivate and influence them to meet study objectives • Proactively manage assigned sites and implement action plans to maintain compliance • Ensure regulatory inspection readiness at assigned clinical sites • Ensure the quality and timely submission of site data, including reporting and follow-up of safety events • Ensure study-subject safety and protection through compliance with monitoring plans, SOPs, guidelines, and regulations • Train study site personnel on study protocols and applicable regulatory requirements • Manage investigator payments according to contractual obligations • Negotiate investigator and hospital agreements • Maintain and complete expense reports according to applicable guidelines • Identify, evaluate, and recommend new investigators and clinical sites

🎯 Requirements

• Appropriate tertiary qualification; a health-related degree or background, such as Medicine, Life Sciences, or Nursing, is preferred • Minimum of 1 to 2 years of experience as a CRA at a pharmaceutical company or CRO • Candidates with approximately 2 years of experience in clinical trials field, particularly within oncology or immunology, can be considered • Experience conducting on-site monitoring of investigational drug or medical device trials is required • Current, in-depth knowledge and understanding of relevant therapeutic indications as they relate to the conduct of clinical trials • Current, in-depth knowledge of regulations governing clinical research, ICH/GCP Guidelines, and applicable local regulations • Strong planning and organizational skills, with the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines • Ability to understand and follow work processes within the assigned function • Strong analytical and conceptual capabilities, interpersonal skills, and the ability to communicate clearly • Ability to address clinical site issues with appropriate guidance, initiate corrective actions, and communicate them effectively • Ability to apply functional expertise and exercise sound judgment • Demonstrated business ethics and integrity

🏖️ Benefits

• Equal opportunity employer • Commitment to operating with integrity, driving innovation, transforming lives, and serving the community