Clinical Research Associate

🔥 7 minutes ago

🏄 California – Remote

🏄 California – Remote

💵 $61.3k - $122.7k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 0%

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Abbott

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1888

🏥 Healthcare

⚕️ Healthcare Insurance

🧬 Biotechnology

Healthcare • Healthcare Insurance • Biotechnology

Abbott is a global healthcare company committed to advancing medical technologies and improving lives around the world. It offers a broad range of leading products in diagnostics, medical devices, nutrition, and branded generic medicines. Abbott's innovations such as the FreeStyle Libre glucose monitoring systems and BinaxNOW rapid antigen tests are transforming diabetes management and COVID-19 response. Through its partnerships and initiatives, Abbott aims to foster health equity, improve access to healthcare, and address critical health challenges like malnutrition and infectious diseases. Abbott is also dedicated to sustainability and social responsibility, striving to make life-changing technologies accessible and affordable.

📋 Description

• Support clinical trial sites from study start-up through closeout • Ensure studies comply with protocols, regulatory requirements, and company procedures • Conduct site qualification, initiation, monitoring, and closeout visits • Train and support investigators, study coordinators, and site staff • Monitor protocol compliance, data quality, and Good Clinical Practice requirements • Review source documents and verify clinical study data accuracy and completeness • Ensure only eligible participants are enrolled • Manage and maintain study and regulatory documentation • Monitor investigational product accountability and inventory • Review adverse event reporting for accuracy and compliance • Assess site performance, including patient recruitment and retention • Prepare monitoring reports and communicate findings, risks, and corrective actions • Build relationships with clinical research sites and internal stakeholders • Develop knowledge of applicable clinical research regulations and study types • Manage assigned tasks and timelines and contribute to study success under general supervision • Report to the Clinical Manager and partner with Clinical Project Teams and Operations leadership

🎯 Requirements

• Bachelor's degree in life sciences or clinical research, or equivalent combination of education and work experience • Minimum 1 year of clinical research experience • Detail-oriented and efficient in time management • Excellent written and verbal communication, organizational, and presentation skills • Ability to work effectively with others • Self-directed and able to work in a fast-paced and constantly changing environment • Ability to multitask, prioritize, and manage time efficiently • Proficient computer skills, including Microsoft Office Suite (Word, Excel, Outlook, etc.) • Ability to travel 40% / travel listed as 50% of the time • Ability to work in a regulated quality environment • Ability to work with human blood or other potentially infectious materials and infectious organisms or known infectious materials • Ability to lift, carry, push, or pull weights over 20 pounds/9 kilos on a regular/daily basis

🏖️ Benefits

• Career development with an international company • Free medical coverage eligibility through the Health Investment Plan (HIP) PPO medical plan in the next calendar year • Retirement savings plan with a high employer contribution • Tuition reimbursement • Freedom 2 Save student debt program • FreeU education benefit toward a bachelor’s degree • Diverse career opportunities • Health and wellness benefits