Remote-Eligible Senior CRA for Complex Trials

BD

Alabama

On-site

USD 90,000 - 120,000

Full time

14 days+
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Job summary

BD is seeking an experienced Senior Clinical Research Associate (Sr. CRA) to manage site monitoring and relationships across multiple clinical studies.

The role emphasizes high-quality study execution, GCP adherence, regulatory compliance, and mentoring of junior CRAs within a fast-paced environment. Responsibilities include site management, monitoring, and documentation using Veeva Vault CTMS/CDMS, while collaborating with internal teams and CROs to ensure successful study delivery.

Qualifications

  • Bachelor’s degree or higher in a healthcare or science-related field.
  • 3 years of field-based CRA experience in the medical device and/or pharmaceutical industry.
  • Thorough knowledge of domestic and international clinical research regulations (ICH GCP, FDA CFR, ISO, HIPAA).

Responsibilities

  • Serve as CRA for assigned complex clinical studies, including site selection, initiation, monitoring, and close-out activities (on-site, virtual, remote).
  • Participate in site feasibility assessments and site selection processes.
  • Ensure study conduct adheres to protocol, regulatory requirements, IRB/EC requirements, and company SOPs.
  • Prioritize patient safety and ensure informed consent is obtained and study procedures are performed ethically.

Skills

CRA experience
Regulatory knowledge
Cross-functional collaboration

Education

Bachelor’s degree or higher in healthcare/science

Tools

Veeva Vault CTMS/CDMS

Job description

BD is seeking an experienced Senior Clinical Research Associate (Sr. CRA) to manage site monitoring and relationships across multiple clinical studies.

The role emphasizes high-quality study execution, GCP adherence, regulatory compliance, and mentoring of junior CRAs within a fast-paced environment. Responsibilities include site management, monitoring, and documentation using Veeva Vault CTMS/CDMS, while collaborating with internal teams and CROs to ensure successful study delivery.

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