Job Description

Job Description

We are the makers of possible

BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics, and the delivery of care. The company develops innovative technology, services and solutions that help advance both clinical therapy for patients and clinical process for health care providers. BD has 70,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.

BD Surgery aims to increase physician satisfaction and to assist hospital and surgery centers to improve outcomes and lower cost with a product portfolio that aligns with the patient’s needs. The business unit focus on preoperative and intraoperative solutions including patient preoperative skin prep, intraoperative irrigation, hemostatic agents and sealants, as well as hernia repair mesh and fixation systems.

The Senior Clinical Research Associate (CRA) will act as a liaison between BD (the study Sponsor) and the sites/clinics that conduct their assigned clinical studies. Focused primarily on ensuring data quality and regulatory compliance, the CRA will work closely with the Principal Investigator and their staff at their assigned clinical study sites. The Senior CRA will identify and/or resolve data queries and will ensure identification and reporting of safety events and/or device deficiencies. Requiring little supervision, the Senior CRA will review site files and processes to ensure that applicable regulations are being followed. They will actively participate in site identification and qualification activities. Assigned studies tend to be larger, more complex studies used to support device registrations.

Responsibilities include, but are not limited to:

• Independently build and maintain successful working relationships with internal partners and site staff (e.g., Principal Investigators, Study Coordinators)
• Acts as the primary liaison between BD and the investigational site
• Perform all types of monitoring visits (i.e., on-site, virtual/remote, in-house) including Pre-Study (Qualification), Site Initiation, Interim, and Close-Out, according to plan
• Conducts source document verification per plan
• Routinely performs site document reviews to ensure compliance with applicable regulations and standards (e.g., GCP/ISO, IRB/EC policies and procedures
• Site interactions involve prioritization of subject safety including appropriately administered informed consent
• Review/report AE/SAEs and protocol deviations per industry and BD standards
• Maintain audit-ready regulatory files for assigned site(s)/project(s) that align with company and industry parameters
• Maintain all project supporting systems, e.g. CTMS, EDC, eTMF, etc
• Produce proficient and timely documentation of monitoring activities/visits (e.g., timely and complete trip reports, contact records, etc. within company-specified quality standards)
• Collaborate with the studies cross-functional team members and actively participate in meetings
• Assist in development and delivery of site-facing presentation materials for Investigator Meetings, Initiation visits, etc.
• Make sure site staff are adequately trained in all project-related requirements and tasks
• Support audit activities, as appropriate
• Ensure site(s) maintains an acceptable inventory of clinical supplies and associated documentation

EDUCATION AND EXPERIENCE

• Bachelor’s Degree or higher in a healthcare or science related field. Consideration of a candidate with any alternate level of education will be case-dependent based on experience and positional need
• Good Clinical Practices (GCP) certification from an accredited program is required
• 2+ years of relevant clinical research experience as a field-based CRA is required; medical device experience is preferred

KNOWLEDGE AND SKILLS

• Fluent knowledge of spoken and written English language, including medical terminology
• Superior written and verbal communication skills
• Proficiency in presentation preparation and delivery
• Technical savviness with an ability to understand the impact technology has on increasing effectiveness and performance
• Previous experience with EDC, CTMS and eTMF systems required
• Understanding of clinical study management processes and systems, including monitoring, investigational product handling, data management, etc.
• Understanding of domestic and international clinical research guidelines, e.g. ICH GCP, FDA CFR, ISO, HIPAA
• Ability to work in and promote team cohesiveness in a virtual/remote environment
• Exhibit flexible organizational change approaches with a growth mindset
• Demonstrated ability to prioritize multiple tasks with challenging timelines and results
• Ability to master understanding of the disease state and product(s) under investigation

For certain roles at BD, employment is contingent upon the Company’s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD’s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.

Why Join Us?

A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It’s also a place where we help each other be great, we do what’s right, we hold each other accountable, and learn and improve every day.

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 health. At BD, you’ll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place.

To learn more about BD visit 

Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of 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, or any other protected status.

Primary Work Location

USA NJ - Franklin Lakes

Additional Locations

Work Shift

NA (United States of America)

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