Clinical Research Associate

🔥 4 minutes ago

🇧🇪 Belgium – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 10%

infoinfo

🗣️🇫🇷 French Required

🗣️🇳🇱 Dutch Required

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Logo of AbbVie

AbbVie

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

• Serve as the primary point of contact for assigned investigative sites • Provide relevant study information and coordinate with internal stakeholders • Build effective working relationships with investigators and site staff • Support understanding of study objectives, protocol, and patient treatment principles • Conduct site evaluation, initiation, routine monitoring, and close-out activities • Support the safety and protection of study participants throughout clinical trials • Develop and adapt site engagement strategies based on study requirements and local site insights • Track site engagement progress and measure impact using available tools • Apply knowledge of protocols, scientific principles, therapeutic areas, and patient journeys to support recruitment, retention, and protocol compliance • Conduct ongoing risk assessments with the Central Monitoring team • Identify study performance or patient safety issues and investigate site risk signals • Ensure preventive and corrective action plans are implemented when required • Ensure timely, quality submission of data and safety information by site personnel • Maintain audit and inspection readiness • Identify and recommend potential investigators and sites • Contribute to assigned initiatives • Mentor and train less experienced Clinical Research Associates

🎯 Requirements

• Degree or equivalent qualification in a health-related discipline, such as Medicine, Life Sciences, Nursing, or a related scientific field • At least one year of clinically related experience • Minimum of six months of experience in clinical research monitoring of investigational drug or device trials • Familiarity with risk-based monitoring approaches, including on-site and remote monitoring • Knowledge of relevant therapeutic areas and ability to apply scientific concepts to clinical trial conduct • Knowledge of local regulatory and legal requirements, ICH/GCP Guidelines, and applicable policies • Fluency in French, Dutch, and English is required • Strong collaboration, communication, active listening, and presentation skills • Strong planning and organizational skills, with ability to manage competing priorities and deadlines • Ability to use technology, monitoring tools, and available resources to support site engagement and study execution • Ability to apply sound judgment, critical thinking, and functional expertise when addressing clinical site issues • Self-motivated and quality-focused, with commitment to integrity and compliance with AbbVie's Code of Business Conduct and Leadership Values

🏖️ Benefits

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

Apply Now

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