Clinical Research Associate II – Neuro & Immunology

🔥 0 minutes ago

🏄 California – Remote

🏄 California – Remote

💵 $84.5k - $162k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🔬 Research Analyst

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AbbVie

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 2013

💊 Pharmaceuticals

🧬 Biotechnology

⚕️ Healthcare Insurance

Pharmaceuticals • Biotechnology • Healthcare Insurance

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

• Considered as the primary point of contact for the investigative site. • Aligns, trains and motivates the site staff and principal investigator on the goals of the clinical trial program. • Conducts site evaluation, site training, routine, and site closure monitoring activities with compliance to the protocol. • Advanced understanding of site engagement and ability to customize site engagement strategy for assigned studies. • Gather local/site insights and utilize site engagement tools to report/track progress and measure impact of that strategy. • Evaluate and ensure effective recruitment and retention techniques/plans based on patient disease journey. • Develop solid knowledge of therapeutic area, asset, and clinical landscape to enable successful patient recruitment. • Ensure quality of data submitted from study sites and assure timely submission of data, including appropriate reporting.

🎯 Requirements

• Appropriate tertiary qualification in health related disciplines (Medical, Scientific, Nursing) preferred. • Minimum of 1 year of clinically related experience, of which a period of 6 months is required in clinical research monitoring of investigational drug or device trials. • Familiarity with risk‐based monitoring approach, onsite and offsite monitoring. • Advanced knowledge of existing and emerging local regulatory and legal requirements, ICH/GCP Guidelines and applicable policies. • Strong cross-functional collaboration skills among internal and external stakeholders. • Strong planning and organizational skills with the ability to work effectively and efficiently in a dynamic environment. • Advanced ability to leverage technology, tools and resources for customer-centric support. • Strong interpersonal skills with excellent written, verbal, active listening, and presentation skills. • Ability to use functional expertise with appropriate guidance and apply good judgment to address clinical site issues. • Self-motivated individual focused on delivering timely and quality outcomes in a fast-paced environment.

🏖️ Benefits

• Paid time off (vacation, holidays, sick) • Medical/dental/vision insurance • 401(k) to eligible employees • Eligible to participate in short-term incentive programs