Clinical Research Associate I

🔥 33 minutes ago

🏄 California – Remote

🏄 California – Remote

💵 $75k - $142.5k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🔬 Research Analyst

🚫👨‍🎓 No degree required

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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 point of contact for investigative sites and provide contextual information on clinical trials • Connect stakeholders with investigative sites and strengthen AbbVie’s positioning • Align, train, and motivate site staff and principal investigators on trial goals, protocols, and patient treatment principles • Conduct site evaluation, site training, routine monitoring, and site closure activities under supervision • Ensure compliance with protocols, monitoring plans, regulations, GCPs, ICH Guidelines, SOPs, and clinical research quality standards • Customize site engagement strategies and use CRM tools to track progress and measure impact • Connect study protocols, scientific principles, and clinical trial requirements to daily execution activities • Evaluate and support effective patient recruitment and retention plans • Develop therapeutic-area, asset, clinical-landscape, and patient-journey knowledge • Conduct continuous risk assessment with the Central Monitoring team to identify study performance and patient safety issues • Resolve site risk signals and implement preventative and corrective action plans • Identify, evaluate, and recommend investigators and clinical sites under supervision • 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 (Medical, Scientific, Nursing) preferred, or equivalent work experience • Clinically related experience, preferably in clinical research coordinating or data management • Knowledge of therapeutic-area indications preferred • Ability to understand and apply scientific concepts to clinical-trial conduct • Knowledge of local regulatory and legal requirements, ICH/GCP Guidelines, and applicable policies • Ability to work collaboratively and cross-functionally • Planning and organizational skills for a dynamic environment with competing projects and deadlines • Ability to leverage technology, tools, and resources for customer-centric site support • Ability to apply functional expertise, critical thinking, and good judgment to clinical-site issues • Strong written, verbal, active-listening, and presentation skills • Ability to establish and leverage site relationships through engagement, motivation, and training • Integrity consistent with AbbVie’s code of business conduct and leadership values • Self-motivated and focused on timely, quality outcomes • Willingness and ability to travel 75% of the time • Candidates from the Southwest, Southeast, and Northeast regions and near a major airport strongly preferred

🏖️ Benefits

• Paid time off (vacation, holidays, sick) • Medical, dental, and vision insurance • 401(k) • Eligibility to participate in short-term incentive programs • Remote work • Equal opportunity employer • Reasonable accommodation for US & Puerto Rico applicants