Principal Clinical Research Associate

🕒 May 12

🦀 Maryland – Remote

🦀 Maryland – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🔬 Research Analyst

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BD

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1897

⚕️ Healthcare Insurance

💊 Pharmaceuticals

🔬 Science

💰 $24M Grant on 2020-07

Healthcare Insurance • Pharmaceuticals • Science

BD (Becton, Dickinson and Company) is a global medical technology company dedicated to advancing the world of health. It focuses on developing innovative technologies, services, and solutions to improve safety and efficiency in healthcare. BD offers a wide range of products including medication management solutions, surgical solutions, cervical cancer screening, drug delivery systems, and laboratory services. The company is also involved in infection risk management and provides advanced clinical insights to enhance patient outcomes. With a commitment to global health sustainability and social investing, BD is a leader in healthcare technology and services worldwide.

📋 Description

• Serve as Lead CRA for assigned complex clinical studies, providing expert oversight of site selection, initiation, monitoring, and close‑out activities • Actively participate in site feasibility assessments and site selection processes • Ensure study conduct is executed according to the clinical protocol, regulatory requirements, IRB/EC requirements, and company SOPs • Prioritize patient safety, ensuring informed consent and study procedures are performed accurately and ethically • Review and report AEs/SAEs and protocol deviations in accordance with regulatory and company requirements • Maintain complete, accurate, and audit‑ready regulatory documentation and TMFs in accordance with ALCOA principles • Monitor site inventory of investigational products and study supplies • Proactively identify, communicate, and manage study risks and issues to ensure operational continuity and compliance • Author, review, and approve Monitoring Plans, study source documents, monitoring tools, and site‑facing training materials • Perform SDR/SDV per monitoring plans and document monitoring activities through timely, high‑quality trip reports • Support interviewing, hiring, onboarding, and training of CRA staff • Present confidently and contribute to extended functional and study team meetings, providing clear updates on site status, risks, and issues

🎯 Requirements

• Bachelor’s degree or higher in a healthcare or science‑related field • Minimum of five (5) years of field‑based CRA experience in the medical device and/or pharmaceutical industry • Experience across multiple phases of clinical research and product development • Experience with IVD and/or POC studies strongly preferred • Laboratory experience in molecular biology, microbiology, or blood culture is highly desirable • Strong understanding of clinical trial operations, monitoring practices, investigational product management, and data management • Thorough knowledge of domestic and international clinical research regulations, including ICH GCP, FDA CFR, ISO, and HIPAA • Proficiency with Veeva Vault CTMS and CDMS required • Excellent written and verbal English communication skills, including medical terminology • Strong presentation, organizational, time‑management, and prioritization skills • Technically savvy with the ability to leverage technology to drive efficiency and performance • Ability to work independently with minimal supervision in a fast‑paced environment

🏖️ Benefits

• Comprehensive Total Rewards program • Competitive package of compensation and benefits programs