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Job Summary
The position will be responsible for managing all clinical research activities performed by the site in compliance with ICH/GCP and country regulations, BD policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of the Sr. CRA, the person will ensure timely and high quality execution and completion of all assigned studies including:

• Monitoring and conducting site visits as per study protocol and local regulatory requirements
• Obtaining informed consent from participants
• Conducting clinical trial conduct according to ICH/GCP and country regulations, BD SOPs, Local Laws & Regulations, Quality Standards and adverse event reporting requirements internally and externally
• Supporting audit/inspection activities as needed
• Submitting case report forms (CRF) electronically or manually
• Communicating with Investigators as needed
• Maintaining accurate and complete documentation
• Working effectively with other roles in the study such as but not limited to CRM, CTC, TA Headquaters, vendors and partners

Responsibilities

• Develop strong relationships with investigators and build trust by operating with integrity, honesty, and openness
• Manage resources (e.g., supplies, equipment, etc.) at sites where necessary
• Identify, attract, recruit, and retain investigators and sites that meet protocol criteria and are capable of fulfilling the required patient enrollment
• Work collaboratively with CRMs and Clinical Trial Coordinators (CTCs) to identify and assess sites and determine site readiness
• Determine site start-up timing based on site readiness and availability of materials/supplies
• Ensure timelines and key milestones are met
• Evaluate site performance and develop strategies for improvement
• Resolve site performance issues and escalate as appropriate
• Identify opportunities for improvement and communicate them to management
• Interact professionally with all external customers (e.g., sites, investigators, vendors, partners)
• Collaborate with internal stakeholders to develop skills and competencies of direct reports

Qualifications
Minimum Requirements:

• Bachelor's degree in Science, Biology, Pharmacy or related field preferred
• 5 years of relevant experience in clinical research
• Experience in clinical trial planning, management and metrics
• Knowledge of Good Documentation Practices
• Ability to work independently and as part of a team
• Strong organizational skills and attention to detail
• Excellent interpersonal, verbal and written communication skills
• Skilled in computer applications (Microsoft Office Suite)

Preferred Qualifications:

• Project Management experience
• Site Management experience
• Team Leadership experience
• CRA Certification

At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.

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 https://bd.com/careers

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.

Required Skills

Optional Skills

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Primary Work Location

USA MD - Sparks - 7 Loveton Circle

Additional Locations

Work Shift

At BD, we are strongly committed to investing in our associates-their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You.

Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates' progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed. The salary or hourly rate offered to a successful candidate is based on experience, education, skills, and any step rate pay system of the actual work location, as applicable to the role or position. Salary or hourly pay ranges may vary for Field-based and Remote roles.

Salary Range Information