Description
AbbVie’s mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care. This is a home-based position with 25% – 50% travel. The Clinical Research Associate (CRA) will play a crucial role in ensuring the successful execution of clinical studies by proactively solving study-related issues and ensuring adherence to protocols and regulations.
Company Culture and Environment
AbbVie emphasizes integrity, innovation, and community service. The workplace fosters diversity and inclusion, promoting a dynamic environment where employees are encouraged to contribute to meaningful projects that improve health outcomes.
Career Growth and Development Opportunities
AbbVie is committed to the professional development of its employees, offering opportunities to work on diverse and impactful clinical trials that can enhance career trajectories in the pharmaceutical R&D field.
Detailed Benefits and Perks
• Comprehensive salary and bonus package
• Health-related benefits including insurance options
• Flexible work arrangements (home-based)
• Professional development opportunities
Compensation and Benefits
Competitive salary along with a bonus and comprehensive benefits package tailored to support health and well-being.
Why you should apply for this position today
Joining AbbVie as a Clinical Research Associate represents an opportunity to contribute to groundbreaking medical research and innovative solutions that have a real impact on patients’ lives. You will become part of a dedicated team that values collaboration and quality, while also enhancing your professional skills in the clinical research space.
Skills
• Strong planning and organizational skills
• Excellent analytical and conceptual capabilities
• Effective interpersonal and communication skills
• In-depth knowledge of clinical research regulations (ICH/GCP)
• Ability to manage clinical site issues proactively
Responsibilities
• Monitor activities of clinical investigative sites to ensure protocol adherence
• Conduct site qualification, initiation, interim monitoring, and closeout visits for Phase 1-4 studies
• Motivate and influence site personnel to meet study objectives
• Ensure regulatory inspection readiness at assigned investigator sites
• Train site personnel on protocol and regulatory requirements
• Identify and evaluate new potential investigative sites
Qualifications
• Appropriate tertiary qualification in health-related fields (e.g., Medical, Scientific, Nursing preferred)
• Significant clinical related experience, including clinical research monitoring
• Current knowledge of therapeutic indications relevant to clinical trials
• Demonstrated business ethics and integrity
Education Requirements
• Bachelor’s degree in a relevant health-related field is preferred.
Education Requirements Credential Category
• Health-related degree (e.g., Medical, Scientific, Nursing)
Experience Requirements
• Experience in monitoring investigational drug or device trials
• Familiarity with federal regulations and GCPs
• Proven track record in managing clinical research processes
Why work in Maidenhead, GBR
Maidenhead offers a harmonious blend of urban and natural environments, providing an appealing lifestyle with access to green spaces and recreational activities. The town is well-connected to major cities and boasts a rich history, making it an attractive place for professionals seeking a vibrant community and career opportunities.
Location: Maidenhead, , GB
Job Posting Language: en
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