Becton, Dickinson and Company

Clinical Research Associate

Becton, Dickinson and Company$75K — $121K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in healthcare, life sciences, or related field
  • Working knowledge of clinical trial processes and data management
  • Familiarity with ICH-GCP, FDA regulations, ISO standards, and HIPAA requirements
  • 2 years of relevant clinical research experience preferred
  • Experience with electronic data capture and clinical trial management systems

Responsibilities

  • Manage and monitor clinical sites for compliance and quality
  • Conduct various monitoring activities through onsite and remote visits
  • Perform source data review and verification as required
  • Develop understanding of study protocols and investigational products
  • Prepare monitoring reports and maintain Trial Master Files
  • Identify and resolve study-related risks and compliance concerns
  • Support site initiation processes and training for site staff

Benefits

  • Opportunity for early-career professionals to gain hands-on experience
  • Collaboration with experienced clinical operations leaders
  • Flexible remote or hybrid work environment
  • 40% travel opportunity broadening professional exposure
  • Focus on professional growth in monitoring expertise
Full Job Description
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.


Primary Work Location
USA MD - Sparks - 7 Loveton Circle

Salary Range Information
$75,800.00 - $121,300.00 USD Annual

About Becton, Dickinson and Company

BD is a global technology company that provides diagnostics and technologies for frontliners. Through their solutions and services, they assist scientists in detecting diseases and advanced researchers' on developing diagnoses and therapeutics. BD was established in 1897 by Farleigh Dickinson and Maxwell Becton in East Rutherford, New Jersey.

Becton, Dickinson and Company Careers

Join the innovative world of Becton, Dickinson and Company (BD), a global medical technology company that is actively seeking driven, dedicated professionals to join our team. At BD, we are committed to advancing the world of health by improving medical discovery, diagnostics, and the delivery of care. This commitment provides the foundation for a workplace where you can engage in meaningful work and where job opportunities abound.

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At BD, you will be part of a culture that values diversity, leadership, and innovation. Our team members are empowered to lead and inspire from day one. Join us and contribute to our mission of advancing the world of health through your professional skills and personal passion.

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Our team at BD is composed of more than 65,000 associates across the globe. These dedicated professionals work at the intersection of technology and healthcare, where they drive innovation and ensure that we stay ahead in a rapidly evolving industry. By joining BD, you will work alongside some of the brightest minds in the industry.

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Start your career with BD through our internship programs or dive straight into a full-time position. We offer a range of opportunities that allow you to explore different areas of our business and find a path that aligns with your career goals. Our hiring process is designed to be transparent and engaging, ensuring that all candidates—whether submitting a resume for an internship or a senior position—feel valued and informed.

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BD is proud to offer competitive benefits that support the health, well-being, and financial security of our employees and their families. From comprehensive health insurance to employee wellness programs and flexible working arrangements, we prioritize the well-being of our team members. Our inclusive culture encourages networking, continuous learning, and the sharing of ideas in a diverse and welcoming environment.

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Learn more about Becton, Dickinson and Company
Size
75,000 employees
Market Cap
$72 billion
Industry
Net Income
$1.6 billion
Founded
1897
5 Year Trend
+9.3%
Revenue
$18.2 billion
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