Becton, Dickinson and Company

Associate Clinical Project Manager

Becton, Dickinson and Company • $70K — $95K *
Tempe, AZ 85281In-Person
Pharmaceuticals & Biotech
Less than 5 years of experience
2 weeks ago
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in life sciences (MA/MS preferred)
  • 3+ years of clinical research experience in medical device, pharmaceutical, or biotechnology sectors
  • Knowledge of domestic and international clinical research regulations and guidelines
  • Proficiency in Microsoft Suite tools (Outlook, Word, Excel, PowerPoint)
  • Strong knowledge of clinical study processes and systems (eTMF, CTMS, CDMS)
  • Effective interpersonal and communication skills
  • Capability to manage multiple tasks and prioritize effectively

Responsibilities

  • Manage quality and compliance of clinical projects according to regulations and standards
  • Plan and strategize clinical strategies with cross-functional teams
  • Demonstrate understanding of therapeutic areas and competitive landscapes
  • Oversee planning and execution of clinical projects to meet timelines and budget
  • Develop Clinical Investigation Plans and essential clinical study documents
  • Manage clinical study budgets and financial reviews
  • Interact with investigational sites and external partners to ensure project success

Benefits

  • Health, dental, and vision insurance
  • Retirement savings plans with company match
  • Paid time off and holidays
  • Professional development opportunities
  • Flexible work arrangements
Full Job Description
Job Description

Job Responsibilities: (Primary Duties, Roles, and/or Authorities)

Under direct manager supervision, the Associate Clinical Project Manager will:

  • Manage the quality and compliance of assigned clinical project(s) ensuring that they meet the highest standards for scientific quality, integrity and ethics and are conducted in accordance with BD global clinical procedures, study protocols, GCP and all applicable regulations.


  • Plan and strategize with other business unit cross functional team members (R&D, Marketing, Quality, and other business partners) to define, implement and execute clinical strategies in support of business objectives.


  • Demonstrate a comprehensive understanding of the therapeutic areas and competitive landscapes for assigned clinical project(s).


  • Oversee the planning and execution of assigned clinical projects to ensure that deliverables are completed on time and within budget. Develop and manage metric reporting tools as needed to track project timelines and deliverables. Provide regular and ad hoc reporting of metrics to Clinical Affairs leadership.


  • Manage activities related to clinical strategy and study design, global applications, submissions, and product launches for assigned clinical project(s) as the clinical subject matter expert.


  • Develop Clinical Investigation Plans (CIPs), Informed Consent Forms (ICFs), Investigator's Brochure's (IBs), Clinical Study Management Plans, Study Process Risk Assessments, Regulatory Management Plans, Case Report Forms (CRFs), Clinical Product Management Plans, Clinical Investigation Reports (CIRs) and other essential clinical study documents.


  • Review and provide input on the development of other essential clinical study documents related to clinical data management, clinical statistics, site management & monitoring, clinical safety management, clinical product management and clinical supplier management.


  • Develop and manage clinical study budgets and monthly financial reviews, including invoice review/approval and accruals for assigned clinical project(s).


  • Manage compliance for required reporting, including but not limited to IDE annual reports, clinicaltrials.gov, and overseas notified bodies/competent authorities.


  • Perform study and/or site-level audits of the Trial Master File (TMF) to ensure that study files are current, accurate, complete and audit-ready.


  • Oversee study and site-level management of the Clinical Trial Management System (CTMS) to ensure that study and site details are current, accurate and complete.


  • Interact with and/or oversee interactions with investigational sites, vendors, key opinion leaders (KOLs) and consultants.


  • Manage external contractors/suppliers for assigned clinical project(s) to ensure that deliverables are completed on-time, within budget, and are consistent with the scope of work.


  • Coach and ensure successful and effective relationships between study teams and investigational site personnel.


  • Provide critical thinking and leadership support for issue escalation related to clinical study activities. Interact with investigational sites, vendors, and other functional areas for issues, as needed. Proactively identify issues and create mitigation strategies in collaboration with Clinical Affairs leadership.


  • Provide support for internal or external audits/inspections and ensure resolution of audit/inspection findings related to assigned clinical projects.


  • Conduct Site Management & Monitoring, Clinical Product Management and Clinical Field support activities/visits, as needed.


  • Conduct, attend, or support training and observational activities, as needed, for study team members.


Education and Experience:

  • Bachelor's Degree (BS/BA) in life sciences (MA/MS preferred)


  • 3+ years of experience in clinical research (medical device, pharmaceutical and/or biotechnology)


Knowledge and Skills:

Required Qualifications:

  • Knowledge of domestic and international clinical research regulations and guidelines, Good Clinical Practice (GCP) and current industry practices related to the conduct of clinical studies


  • Proficiency with Microsoft Suite tools (Outlook, Word, Excel, PowerPoint, OneNote, To-Do, SharePoint, etc.)


  • Strong knowledge of clinical study processes and systems (eTMF, CTMS and CDMS)


  • Strong interpersonal and communication (oral and written) skills


  • Strong organizational skills, attention to detail, critical thinking and analytical skills


  • Able to manage and delegate multiple tasks and prioritize importance of tasks/projects


  • Ability to understand and interpret technical, scientific, and clinical information as it applies to product approval activities


  • Ability to lead teams to translate issues into actions, make decisions and influence outcomes


  • Ability to travel up to 40% (or more during peak times)


Preferred Qualifications:

  • Prior experience with clinical studies related to peripheral vascular diseases, end-stage kidney disease and/or oncology


  • Prior experience managing clinical projects (strongly preferred)


  • Experience with medical device studies (strongly preferred)


  • Prior experience with site management & monitoring


  • Prior experience with Veeva Vault Clinical Suite (CTMS, CDMS and eTMF)


  • Professional certification through one or more relevant associations (e.g., ACRP, SOCRA, etc.)


Physical Demands: (if applicable)

While performing the duties of this job, the employee is regularly required to stand, walk, sit, use sight, and use hands to manipulate, handle or feel objects, tools, controls, and office equipment. The employee frequently is required to verbally communicate with other associates. The employee is occasionally required to reach with hands and arms and stoop, kneel or crouch.

Work Environment: (if applicable)

While performing the duties of this job, the employee may be in an open cubicle environment. Candidate must be able to work in a team-oriented, fast-paced environment.

Primary Work Location
USA AZ - Tempe Headquarters

Additional Locations

Work Shift

About Becton, Dickinson and Company

BD is a global technology company that provides diagnostics and technologies for frontliners. Through their solutions and services, they assist scientists in detecting diseases and advanced researchers' on developing diagnoses and therapeutics. BD was established in 1897 by Farleigh Dickinson and Maxwell Becton in East Rutherford, New Jersey.

Becton, Dickinson and Company Careers

Join the innovative world of Becton, Dickinson and Company (BD), a global medical technology company that is actively seeking driven, dedicated professionals to join our team. At BD, we are committed to advancing the world of health by improving medical discovery, diagnostics, and the delivery of care. This commitment provides the foundation for a workplace where you can engage in meaningful work and where job opportunities abound.

Work You’ll Do

At BD, you will be part of a culture that values diversity, leadership, and innovation. Our team members are empowered to lead and inspire from day one. Join us and contribute to our mission of advancing the world of health through your professional skills and personal passion.

Transform Your Career

BD offers a unique position in the marketplace that combines industry expertise, leadership in medical innovation, and a collaborative culture to help you grow your career. Whether you are looking for an entry-level position or a more senior role, we provide the tools and support for your professional growth through comprehensive training and development programs.

Innovative Work Environment

Our team at BD is composed of more than 65,000 associates across the globe. These dedicated professionals work at the intersection of technology and healthcare, where they drive innovation and ensure that we stay ahead in a rapidly evolving industry. By joining BD, you will work alongside some of the brightest minds in the industry.

Internship and Employment Opportunities

Start your career with BD through our internship programs or dive straight into a full-time position. We offer a range of opportunities that allow you to explore different areas of our business and find a path that aligns with your career goals. Our hiring process is designed to be transparent and engaging, ensuring that all candidates—whether submitting a resume for an internship or a senior position—feel valued and informed.

Benefits and Culture

BD is proud to offer competitive benefits that support the health, well-being, and financial security of our employees and their families. From comprehensive health insurance to employee wellness programs and flexible working arrangements, we prioritize the well-being of our team members. Our inclusive culture encourages networking, continuous learning, and the sharing of ideas in a diverse and welcoming environment.

Join Our Team

Explore the job opportunities at BD and discover how your expertise can help shape the future of healthcare. Search open positions that match your skills and interests. We look for passionate, curious, creative, and solution-driven team players.

Stay Connected

Keep up to date with career tips, insider perspectives, and industry-leading insights you can put to use today—all from the people who work here. Personalize your subscription to receive job alerts, latest news, and insider tips tailored to your preferences. See what exciting and rewarding opportunities await at Becton, Dickinson and Company.

Explore Careers at BD

Whether you're preparing for your first interview or looking to advance into a leadership role, BD offers career paths that foster continuous growth and innovation. Join us in our mission to improve medical outcomes and enhance patient care worldwide.

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At Becton, Dickinson and Company, we are more than just a company; we are a community that is dedicated to making a difference in the lives of people all around the world.
Learn more about Becton, Dickinson and Company
Size
75,000 employees
Market Cap
$72 billion
Industry
Healthcare
Net Income
$1.6 billion
Founded
1897
5 Year Trend
+9.3%
Revenue
$18.2 billion
NASDAQ
BDX
* Ladders Estimates

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