Sr. Clinical Research Associate

BD; Alabama; On-site; USD 90,000 - 120,000; Full time

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

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.

Summary

Job Description

The Senior Clinical Research Associate (Sr. CRA) is an experienced clinical operations professional responsible for managing site monitoring and relationship activities across multiple clinical studies. This role serves as a key resource to study teams, ensuring high-quality study execution, adherence to Good Clinical Practice (GCP), regulatory requirements, and company standards. The Sr. CRA provides guidance to less experienced CRAs, supports investigator sites, proactively identifies and resolves operational issues, and contributes to the successful delivery of clinical study objectives.

The Sr. CRA will practice excellent written and verbal communication skills, including medical terminology. In this role the candidate will display strong presentation, organizational, time‑management, and prioritization skills. Being technically savvy with the ability to leverage technology to drive efficiency and performance while working independently with minimal supervision in a fast‑paced environment will be key.

Responsibilities

Study & Site Management

• Serve as CRA for assigned complex clinical studies, providing expert oversight of site selection, initiation, monitoring, and close‑out activities (on‑site, virtual, remote).


• Actively participate in site feasibility assessments and site selection processes.


• Ensure study conduct is executed according to the clinical protocol, regulatory requirements (GCP, FDA, ISO), 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.

Monitoring & Documentation

• 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.


• Ensure compliance with company travel and expense policies.

Leadership & Mentorship

• Provide mentoring, training, and functional oversight of CRAs, including contingent (contract) CRAs.


• Lead or review functional job aids and training materials.


• Present confidently and contribute to extended functional and study team meetings, providing clear updates on site status, risks, and issues.

Systems & Collaboration

• Utilize and maintain accurate study data in clinical systems, including Veeva Vault CTMS and CDMS.


• Work cross‑functionally with internal teams and CROs to ensure high‑quality study execution and oversight.


• Build and maintain effective working relationships with investigator sites and internal stakeholders.

Minimum Qualifications

• Bachelor’s degree or higher in a healthcare or science‑related field. (Alternate education levels may be considered based on experience and business need)


• 3 years of field‑based CRA experience in the medical device and/or pharmaceutical industry.


• 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.

Preferred Knowledge & Skills

• Experience with IVD and/or POC studies.


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


• Proficiency with Veeva Vault CTMS and CDMS

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 visit https://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.

Required Skills

Optional Skills

Primary Work Location

USA MD - Sparks - 7 Loveton Circle

Additional Locations

Work Shift

NA (United States of America)

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.

Salary Range Information