Senior Clinical Research Associate

🔥 0 minutes ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

🇬🇧 UK Skilled Worker Visa Sponsor

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

👻 Ghost score 10%

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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

• Advance AbbVie's clinical research pipeline and support innovative medicines and solutions • Serve as the primary sponsor point of contact for investigative sites • Partner with study teams, internal R&D stakeholders, investigators, and site staff • Align, train, and motivate site staff and principal investigators on trial goals, protocols, and patient treatment principles • Mentor and support junior CRAs on site management activities and professional development • 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, SOPs, and quality standards • Develop and apply customized site engagement strategies • Gather local and site insights and track engagement progress and impact • Develop recruitment and retention techniques based on the patient disease journey • Build knowledge of therapeutic areas, assets, clinical landscapes, and patient journeys • 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 clinical trial sites • Ensure quality and timely submission of site data and safety event reporting • Maintain audit and regulatory inspection readiness • 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 • Minimum of 3 years of clinically related experience • 2 years preferable in independent clinical research monitoring of investigational drug or device trials • Familiarity with risk-based monitoring approach, onsite and offsite monitoring • Knowledge of therapeutic area indications and scientific concepts related to clinical trials • Knowledge of local regulatory and legal requirements, ICH/GCP Guidelines and applicable policies • Advanced communication and cross-functional collaboration skills • Superior planning and organizational skills • Ability to work effectively in a dynamic environment with competing projects and deadlines • Ability to leverage technology, tools and resources • Excellent written, verbal, active listening and presentation skills • Ability to independently address clinical site issues using functional expertise and critical thinking • Ability to act with integrity in accordance with AbbVie code of business conduct and leadership values • Self-motivated and focused on timely, quality outcomes

🏖️ Benefits

• Remote work option • Equal opportunity employment • Veteran and disability inclusion commitment