Clinical Research Associate

We are the people who give possibilities purpose

BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.

Job Description

Summary:

The Clinical Research Associate (CRA) is responsible for the management and monitoring of assigned clinical research studies and investigative sites. This role ensures studies are conducted in compliance with Good Clinical Practice (GCP), applicable regulatory requirements, company policies, and established quality standards.

The CRA will collaborate closely with cross-functional teams and study sites to support the successful execution of clinical research activities. This position offers an excellent opportunity for early-career clinical research professionals to develop monitoring expertise through hands-on site management, study oversight, and collaboration with experienced clinical operations leaders. This role requires approximately 40% travel.

The CRA will have strong organizational, communication, and site management skills and the ability to manage multiple priorities and meet competing deadlines in a fast-paced environment. They will work independently while fostering teamwork in a remote or hybrid environment.

Responsibilities

• Manage and monitor assigned clinical sites and studies to ensure compliance, quality, and operational success.

• Conduct monitoring activities, including qualification, initiation, routine monitoring, and closeout visits through onsite, remote, virtual, or in-house methods.

• Perform source data review (SDR) and source data verification (SDV) according to study requirements.

• Develop a comprehensive understanding of study protocols, investigational products, instructions for use (IFU), and related study documentation.

• Review and contribute to monitoring plans, study source documents, and other study-related materials.

• Ensure sites conduct clinical studies in compliance with protocol requirements, GCP, ISO standards, regulatory requirements, and IRB/EC policies.

• Prioritize patient safety and verify proper informed consent procedures are followed and documented.

• Support site feasibility assessments and site selection activities.

• Prepare timely, accurate, and high-quality monitoring reports, visit documentation, and communication records.

• Facilitate site initiation visits and support the development and delivery of site-facing training and presentation materials.

• Identify, communicate, and help resolve study risks, issues, and compliance concerns.

• Participate in study team meetings and provide regular updates regarding site status, performance, risks, and progress.

• Maintain Trial Master Files (TMF) and ensure timely site closeout activities.

Required Qualifications

• Bachelor's degree or higher in healthcare, life sciences, or related scientific discipline.

• Working knowledge of clinical trial processes, monitoring activities, data management, and investigational product handling.

• Knowledge of applicable regulations and guidelines, including ICH-GCP, FDA regulations, ISO standards, and HIPAA requirements.

Preferred Qualifications & Skills

• 2 years of Clinical Research Associate experience, Clinical Research Coordinator experience, or relevant laboratory experience supporting clinical research, diagnostics, biotechnology, medical device, or pharmaceutical studies.

• Experience supporting diagnostic, in vitro diagnostic (IVD), point-of-care (POC), molecular biology, microbiology, or laboratory-based clinical studies.

• Laboratory experience in molecular biology, microbiology, or blood culture testing.

• Experience working with electronic data capture (EDC), clinical trial management systems (CTMS), and electronic Trial Master File (eTMF) platforms.

• Experience with Veeva Vault TMF and/or Veeva CDMS platforms.

What Makes You Successful

• Strong attention to detail and commitment to quality.

• Ability to build relationships with investigative sites and internal stakeholders.

• Excellent organizational and time-management skills.

• Strong written and verbal communication skills.

• Adaptability and willingness to learn in a fast-paced clinical research environment.

Why Join Us?

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive.

We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.

To learn more about BD visithttps://bd.com/careers.

Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.

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At BD, we reward, support and develop our associates through our comprehensive Total Rewards program. We are committed to attracting and retaining high quality talent by providing reward and recognition opportunities that promote a performance-based culture, as well as a competitive package of compensation and benefits programs. You can learn more on our career site under " Our Commitment to You."

Our salary or hourly rate ranges reward associates fairly and competitively. We regularly review these ranges and factors, such as location, contribute to the range displayed.

Our pay is based on the role and the necessary skills and education to perform it successfully. The salary or hourly rate offered is determined by the role's specific requirements, including any applicable step rate pay system at the work location. Salary or hourly pay ranges are influenced by labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location which may also affect the workplace arrangement of the role.

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