Clinical Research Associate II – Immunology

🔥 7 minutes ago

🐊 Florida – Remote

🐊 Florida – Remote

💵 $75k - $142.5k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🚫👨‍🎓 No degree required

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 0%

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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 by turning science into medicine and leveraging advanced capabilities • Serve as the primary point of contact for investigative sites • Provide clinical trial context and connect stakeholders with investigative sites • Align, train, and motivate site staff and principal investigators on trial goals, protocols, and patient treatment principles • Conduct site evaluation, training, routine monitoring, and site closure activities • Ensure compliance with protocols, monitoring plans, applicable regulations, GCPs, ICH Guidelines, AbbVie SOPs, and quality standards • Develop and customize site engagement strategies and use CRM tools to track progress and measure impact • Support effective patient recruitment and retention based on the patient disease journey • Develop knowledge of the therapeutic area, clinical asset, clinical landscape, and patient journey • Mentor and train less experienced CRAs and contribute to their development • Participate in global or local task forces and initiatives • Conduct continuous risk assessment with the Central Monitoring team to identify study performance or patient safety issues • 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 contract obligations, when applicable

🎯 Requirements

• Appropriate tertiary qualification in health-related disciplines (Medical, Scientific, Nursing) preferred • Minimum of 1 year of clinically related experience • At least 6 months of clinical research monitoring experience involving investigational drug or device trials • Familiarity with risk-based monitoring, including onsite and offsite monitoring • Knowledge of applicable therapeutic area indications preferred • Advanced knowledge of local regulatory and legal requirements, ICH/GCP Guidelines, and applicable policies • Strong cross-functional collaboration, planning, organizational, interpersonal, written, verbal, active listening, and presentation skills • Ability to work effectively in a dynamic environment with competing projects and deadlines • Advanced ability to leverage technology, tools, and resources • Ability to establish site relationships and trusted partnerships through engagement, motivation, and training • Ability to apply critical thinking and good judgment to clinical site issues • Integrity in accordance with AbbVie’s code of business conduct and leadership values • Self-motivated approach focused on timely, quality outcomes

🏖️ Benefits

• Paid time off including vacation, holidays, and sick leave • Medical, dental, and vision insurance • 401(k) • Short-term incentive programs • Equal opportunity employment • Reasonable accommodations for US and Puerto Rico applicants