Clinical Research Associate

🔥 7 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.

👻 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

• 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, GCP, ICH Guidelines, AbbVie SOPs, and quality standards • Develop and adapt site-engagement strategies; gather site insights and track strategy progress and impact • Support effective patient recruitment and retention plans based on the patient disease journey • Maintain therapeutic-area, asset, clinical-landscape, and patient-journey knowledge • Participate in or lead global and local task forces and initiatives • Perform assigned activities and conduct continuous proactive risk assessment with the Central Monitoring team • Identify and resolve site-risk signals and implement preventative and corrective action plans • Identify, evaluate, and recommend potential investigators and sites for 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 • Familiar with risk-based monitoring approach, onsite and offsite monitoring • Knowledge of appropriate therapeutic area indications and ability to apply scientific concepts to clinical trials • Knowledge of local regulatory and legal requirements, ICH/GCP Guidelines and applicable policies • Advanced communication and 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, presentation, and interpersonal skills • Ability to establish and leverage site relationships through engagement, motivation, and training • Ability to independently address clinical site issues using functional expertise, critical thinking, and judgment • Ability to act with integrity in accordance with AbbVie’s code of business conduct and leadership values • Self-motivated and focused on timely, quality outcomes in a fast-paced environment

🏖️ Benefits

• Excellent development opportunities • Reward and benefits package • Accessible Maidenhead office with large car park • Step-free entry, accessible restrooms, and elevators • Assistive technologies and adaptable workstations • Dedicated quiet zone • Equal opportunity and inclusive work environment