Clinical Research Associate

🔥 0 minutes ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🚫👨‍🎓 No degree required

🇬🇧 UK Skilled Worker Visa Sponsor

This company has sponsored UK Skilled Worker visas in the past.

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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

• Serve as the primary sponsor point of contact for investigative sites • Provide contextual information on clinical trials and connect stakeholders with investigative sites • Align, train, and motivate site staff and principal investigators on trial goals, protocols, and patient treatment principles • Support, guide, and mentor junior personnel on site management activities • Conduct site evaluation, site training, routine on-site and off-site monitoring, and site closure monitoring • Ensure compliance with protocols, monitoring plans, regulations, GCPs, ICH Guidelines, SOPs, and quality standards • Customize site engagement strategies and track their progress and impact • Gather local and site insights • Connect study protocols and scientific principles to day-to-day trial execution • Develop and ensure effective patient recruitment and retention techniques and plans • Build therapeutic-area, asset, clinical-landscape, and patient-journey knowledge to support recruitment and protocol compliance • Participate in or lead global and local task forces and initiatives • Conduct continuous risk assessment with the Central Monitoring team • Identify and resolve site risk signals and implement preventative and corrective action plans • Identify, evaluate, and recommend investigators and sites for planned clinical studies • Ensure quality and timely submission of site data, including safety-event reporting and follow-up • Maintain audit and regulatory inspection readiness at assigned sites • Manage investigator payments according to executed contract obligations, as applicable

🎯 Requirements

• Appropriate tertiary qualification in health related disciplines (e.g., Medical, Scientific, Pharmacy, Nursing) preferred or experience • Independent clinical research monitoring experience of investigational drug or device trials in any therapeutic area • Familiarity with risk-based monitoring approach, onsite and offsite monitoring • Knowledge of appropriate therapeutic area indications and ability to understand and apply scientific concepts to clinical trials • Knowledge of existing and emerging local regulatory and legal requirements, ICH/GCP Guidelines, and applicable policies • Advanced communication skills and superior cross-functional collaboration skills • Strong planning and organizational skills; ability to work effectively with competing projects and deadlines • Ability to leverage technology, tools, and resources for customer-centric site support • Excellent written, verbal, active listening, and presentation skills • Ability to establish and leverage site relationships and trusted partnerships through engagement, motivation, and training • Ability to independently use functional expertise, critical thinking, and good judgment to address clinical site issues • Integrity in accordance with AbbVie code of business conduct and leadership values • Self-motivated approach focused on timely, quality outcomes in a fast-paced environment

🏖️ Benefits

• Excellent development opportunities • Reward and benefits package • Large car park for easy access • Step-free entry, accessible restrooms, and elevators • Assistive technologies and adaptable workstations • Dedicated quiet zone • Equal opportunity employer committed to accessibility and employee well-being