Clinical Research Associate I – Neurology

🔥 13 hours ago

🏄 California – Remote

🏄 California – 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%

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.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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 supporting excellence in clinical research • Partner with investigators and site staff to support effective clinical-trial engagements • Serve as the primary point of contact for investigative sites • Provide information on clinical trials and connect stakeholders with investigative sites • Align, train, and motivate site staff and principal investigators under supervision • Conduct site evaluation, training, routine monitoring, and site-closure activities under supervision • Ensure compliance with protocols, monitoring plans, regulations, GCPs, ICH Guidelines, SOPs, and quality standards • Customize site-engagement strategies for assigned studies under supervision • Gather local and site insights and use CRM tools to track progress and measure impact • Connect study protocols, scientific principles, and clinical-trial requirements to day-to-day execution • Evaluate and support patient recruitment and retention plans • Develop therapeutic-area, asset, clinical-landscape, and patient-journey knowledge • Conduct continuous risk assessment with the Central Monitoring team • Resolve site risk signals and address clinical-site issues • Implement preventative and corrective action plans to mitigate risk and promote compliance • Identify, evaluate, and recommend investigators and sites under supervision • 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

🎯 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 • Knowledge of local regulatory and legal requirements, ICH/GCP Guidelines, and applicable policies • Ability to work collaboratively and cross-functionally • Planning and organizational skills • Ability to work effectively in a dynamic environment with competing projects and deadlines • Ability to leverage technology, tools, and resources • Critical-thinking and good-judgment skills • Strong written, verbal, active listening, and presentation skills • Ability to establish and leverage site relationships and trusted partnerships • Ability to act with integrity in accordance with AbbVie’s code of business conduct and leadership values • Self-motivated and focused on delivering timely, quality outcomes • Work authorization in the United States is implied by the US-based role and applicant provisions

🏖️ Benefits

• Paid time off (vacation, holidays, sick) • Medical, dental, and vision insurance • 401(k) • Short-term incentive programs • Equal opportunity employer • Reasonable accommodations for applicants • Veterans and disability-inclusive employment practices