BD
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.
Senior Clinical Research Associate
🕒 2 days ago
📊 Check your resume score for this job
Improve your chances of getting an interview by checking your resume score before you apply.
BD
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
• Independently build and maintain successful working relationships with internal partners and site staff • Acts as the primary liaison between BD and the investigational site • Perform all types of monitoring visits • Conducts source document verification per plan • Routinely performs site document reviews to ensure compliance with applicable regulations and standards • Review/report AE/SAEs and protocol deviations per industry and BD standards • Maintain audit-ready regulatory files for assigned site(s)/project(s) • Produce proficient and timely documentation of monitoring activities/visits • Collaborate with the studies cross-functional team members and actively participate in meetings
🎯 Requirements
• Bachelor’s Degree or higher in a healthcare or science related field AND 2+ years of relevant clinical research experience is required • Good Clinical Practices (GCP) certification from an accredited program is required • Fluent knowledge of spoken and written English language, including medical terminology • Proficiency in EDC, CTMS, and eTMF systems required • Understanding of clinical study management processes and systems, including monitoring, investigational product handling, data management, etc.
🏖️ Benefits
• Health insurance • 401(k) matching • Professional development opportunities • Paid time off
Apply NowSimilar Jobs
🕒 3 days ago
Research Analyst contributing to Child Care Aware of America’s state licensing and quality rating projects. Involves data collection, analysis, and relationship development with stakeholders.
🕒 3 days ago
Senior Clinical Research Associate managing research activities at clinical study sites. Involved in all study stages, ensuring compliance and site training while based in the United States.
🕒 3 days ago
Senior Clinical Research Associate managing clinical research activities across diverse therapeutic areas. Collaborating with teams to ensure compliance and support clinical studies effectively.
🕒 3 days ago
Clinical Research Associate managing clinical studies for Worldwide Clinical Trials. Collaborating with diverse teams to drive scientific breakthroughs in various therapeutic areas.
🕒 3 days ago
Senior Clinical Research Associate managing the research activities at sites for Worldwide Clinical Trials. Collaborating across diverse therapeutic areas and ensuring study compliance and success.
