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Becton Dickinson

Global medical devices, lab equipment supplier

Medical Affairs Senior Manager

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeFranklin Lakes, NJ, USA$172k - $275.2k /yr

About the Job

Requirements

  • Be a licensed healthcare practitioner, such as a registered nurse, physician assistant, or nurse practitioner.
  • Have a minimum bachelor's degree in a science-related field.
  • Have a minimum of 5 years of experience in human clinical trials.
  • Have a minimum of 5 years of experience in program management activities and people management.
  • Have excellent communication and presentation skills and be able to interact productively with internal and external customers.
  • Be able to anticipate and resolve problems.
  • Be able to lead cross-functional efforts and teams.
  • Be able to work independently and collaboratively within a team.
  • Be able to write clearly and analytically.
  • Be fluent in English.
  • Be onsite daily in Franklin Lakes, New Jersey.

Responsibilities

  • Provide leadership and assistance to EP ASCP and ASVP staff and allied associates on matters pertaining to the Programs’ services, policies, procedures, and staff, as directed by the VP, EP.
  • Hire, evaluate, and manage EP associates, contractors, and/or vendor personnel who engage in Program activities, as assigned.
  • Work alongside the Director, EP to support global or regional locations or Business Units that wish to expand Program activities in existing or new locations.
  • Handle all submissions and communications with the ASCP Institutional Review Board and Ethics Committee.
  • Provide monitoring expertise to the project team and effectively manage assigned clinical sites and projects.
  • Oversee and ensure site staff execute protocols according to plan and comply with regulatory requirements and standards, including Good Clinical Practice and ISO, Institutional Review Board and Ethics Committee policies and procedures, and BD established standards.
  • Prioritize subject safety and ensure informed consent procedures are carried out and documented properly.
  • Maintain complete, audit-ready regulatory files for assigned sites and projects that comply with company and industry parameters, such as ALCOA.

Desired Qualifications

  • Experience in Good Clinical Practice is preferred.
  • A minimum of 3 years of experience in site monitoring is preferred.
  • Certifications in clinical trial management from recognized training entities are a plus.

About the Company

Becton Dickinson

Global medical devices, lab equipment supplier

BD (Becton, Dickinson and Company) is a global medical technology company that designs, manufactures, and sells medical devices, laboratory equipment, and related services for hospitals, labs, clinicians, and biopharma partners. It operates in four segments: Medical Essentials (medication delivery and specimen management devices), Connected Care (medication management and advanced patient monitoring systems), BioPharma Systems (drug delivery systems for pharmaceutical partners), and Interventional (surgical, endovascular, urological, and critical care products). In addition to devices, BD offers connected software, analytics, clinical education, customer portals, and service programs to support its products. The company’s goal is to help healthcare providers improve patient outcomes by enabling safer and more efficient delivery of care through integrated devices, data, and services across the health ecosystem.

Company size
10,001+
Company stage
IPO
Headquarters
Franklin Lakes, NJ
Founded
1961

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