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Becton Dickinson logo

Senior Clinical Project Manager

Becton Dickinson

Senior Clinical Project Manager

Becton Dickinson logo

Becton Dickinson

full-time

Posted: November 17, 2025

Number of Vacancies: 1

Job Description

Job Description Summary

You will lead the planning, execution, and completion of clinical studies for BD Biosciences, ensuring all activities meet regulatory and quality standards. You will guide studies from initial concept through closeout, collaborating with medical, scientific, and operational teams. The role requires overseeing study design, site activities, budgets, and compliance with Good Clinical Practices and regional regulations. In this role, you can expect to travel up to 30% of the time. The remaining work hours will be spent onsite in Limerick, with one day per week working from home.

OUR VISION FOR BDB AT BD
BD Biosciences (BDB) is a leading provider of high-quality flow cytometry and single-cell genomics solutions, scientific research and clinical laboratories. Here, we are leading the way by developing the best technologies that have the ability to look closer at the details of cells and diseases.

Job Description

We are the makers of possible

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.

Why join us?

A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.

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.

Become a maker of possible with us!

Main responsibilities will include:

  • Lead clinical trials from planning through completion, ensuring adherence to study timelines and quality standards.
  • Prepare and review key study documents, including protocols, consent forms, investigator brochures, and training materials.
  • Manage relationships with study sites, external laboratories, and service providers, ensuring smooth study conduct.
  • Monitor study progress, budgets, and resources, adapting plans to meet study complexity and milestones.
  • Define and track key study metrics and ensure study data is collected and reported accurately.
  • Conduct site visits as required, oversee staff training, and support study audits.
  • Identify potential risks to study timelines and outcomes and implement mitigation plans.
  • Mentor less experienced team members and support cross-functional collaboration.

About you:

  • Bachelor’s or master’s degree in biological sciences, biomedical engineering, or related field; advanced degrees preferred.
  • Minimum five years of experience in medical device clinical development, with direct experience managing clinical studies.
  • Strong understanding of regulatory requirements, GCP, IVDR, and GDPR.
  • Experience with BD Biosciences flow cytometry systems and reagents preferred.
  • Excellent verbal and written communication skills, able to prepare and review complex documents.
  • Proficiency in MS Office and familiarity with clinical trial databases and flow cytometry software is a plus.
  • We welcome applications from senior professionals in Clinical Laboratories or Clinical Research Organizations, even if they have no prior industry experience.

Click on apply if this sounds like you!

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.

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.

To learn more about BD visit: https://bd.com/careers

Required Skills

Optional Skills

.

Primary Work Location

IRL Limerick - Castletroy

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 determined by their experience, education, and skills, as well as the labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location.

Salary Range Information

€73,500.00 - €125,000.00 EUR Annual

Locations

  • Limerick, Limerick, Ireland

Salary

Estimated Salary Rangemedium confidence

75,000 - 110,000 EUR / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • proficiency in MS Officeintermediate
  • familiarity with clinical trial databasesintermediate
  • familiarity with flow cytometry softwareintermediate
  • Excellent verbal and written communication skillsintermediate
  • Strong understanding of regulatory requirementsintermediate
  • direct experience managing clinical studiesintermediate

Required Qualifications

  • Bachelor’s or master’s degree in biological sciences, biomedical engineering, or related field; advanced degrees preferred. (degree in master)
  • Minimum five years of experience in medical device clinical development, with direct experience managing clinical studies. (experience)
  • Strong understanding of regulatory requirements, GCP, IVDR, and GDPR. (experience)
  • Experience with BD Biosciences flow cytometry systems and reagents preferred. (experience)
  • Excellent verbal and written communication skills, able to prepare and review complex documents. (experience)
  • Proficiency in MS Office and familiarity with clinical trial databases and flow cytometry software is a plus. (experience)
  • We welcome applications from senior professionals in Clinical Laboratories or Clinical Research Organizations, even if they have no prior industry experience. (experience)

Preferred Qualifications

  • advanced degrees preferred. (degree)
  • Experience with BD Biosciences flow cytometry systems and reagents preferred. (experience)
  • Proficiency in MS Office and familiarity with clinical trial databases and flow cytometry software is a plus. (experience)

Responsibilities

  • Lead clinical trials from planning through completion, ensuring adherence to study timelines and quality standards.
  • Prepare and review key study documents, including protocols, consent forms, investigator brochures, and training materials.
  • Manage relationships with study sites, external laboratories, and service providers, ensuring smooth study conduct.
  • Monitor study progress, budgets, and resources, adapting plans to meet study complexity and milestones.
  • Define and track key study metrics and ensure study data is collected and reported accurately.
  • Conduct site visits as required, oversee staff training, and support study audits.
  • Identify potential risks to study timelines and outcomes and implement mitigation plans.
  • Mentor less experienced team members and support cross-functional collaboration.

Benefits

  • general: A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture.
  • general: You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.
  • general: At BD, you’ll discover a culture in which you can learn, grow and thrive.
  • general: And find satisfaction in doing your part to make the world a better place.
  • general: 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.
  • general: 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.

Travel Requirements

0%

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Becton Dickinson logo

Senior Clinical Project Manager

Becton Dickinson

Senior Clinical Project Manager

Becton Dickinson logo

Becton Dickinson

full-time

Posted: November 17, 2025

Number of Vacancies: 1

Job Description

Job Description Summary

You will lead the planning, execution, and completion of clinical studies for BD Biosciences, ensuring all activities meet regulatory and quality standards. You will guide studies from initial concept through closeout, collaborating with medical, scientific, and operational teams. The role requires overseeing study design, site activities, budgets, and compliance with Good Clinical Practices and regional regulations. In this role, you can expect to travel up to 30% of the time. The remaining work hours will be spent onsite in Limerick, with one day per week working from home.

OUR VISION FOR BDB AT BD
BD Biosciences (BDB) is a leading provider of high-quality flow cytometry and single-cell genomics solutions, scientific research and clinical laboratories. Here, we are leading the way by developing the best technologies that have the ability to look closer at the details of cells and diseases.

Job Description

We are the makers of possible

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.

Why join us?

A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.

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.

Become a maker of possible with us!

Main responsibilities will include:

  • Lead clinical trials from planning through completion, ensuring adherence to study timelines and quality standards.
  • Prepare and review key study documents, including protocols, consent forms, investigator brochures, and training materials.
  • Manage relationships with study sites, external laboratories, and service providers, ensuring smooth study conduct.
  • Monitor study progress, budgets, and resources, adapting plans to meet study complexity and milestones.
  • Define and track key study metrics and ensure study data is collected and reported accurately.
  • Conduct site visits as required, oversee staff training, and support study audits.
  • Identify potential risks to study timelines and outcomes and implement mitigation plans.
  • Mentor less experienced team members and support cross-functional collaboration.

About you:

  • Bachelor’s or master’s degree in biological sciences, biomedical engineering, or related field; advanced degrees preferred.
  • Minimum five years of experience in medical device clinical development, with direct experience managing clinical studies.
  • Strong understanding of regulatory requirements, GCP, IVDR, and GDPR.
  • Experience with BD Biosciences flow cytometry systems and reagents preferred.
  • Excellent verbal and written communication skills, able to prepare and review complex documents.
  • Proficiency in MS Office and familiarity with clinical trial databases and flow cytometry software is a plus.
  • We welcome applications from senior professionals in Clinical Laboratories or Clinical Research Organizations, even if they have no prior industry experience.

Click on apply if this sounds like you!

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.

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.

To learn more about BD visit: https://bd.com/careers

Required Skills

Optional Skills

.

Primary Work Location

IRL Limerick - Castletroy

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 determined by their experience, education, and skills, as well as the labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location.

Salary Range Information

€73,500.00 - €125,000.00 EUR Annual

Locations

  • Limerick, Limerick, Ireland

Salary

Estimated Salary Rangemedium confidence

75,000 - 110,000 EUR / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • proficiency in MS Officeintermediate
  • familiarity with clinical trial databasesintermediate
  • familiarity with flow cytometry softwareintermediate
  • Excellent verbal and written communication skillsintermediate
  • Strong understanding of regulatory requirementsintermediate
  • direct experience managing clinical studiesintermediate

Required Qualifications

  • Bachelor’s or master’s degree in biological sciences, biomedical engineering, or related field; advanced degrees preferred. (degree in master)
  • Minimum five years of experience in medical device clinical development, with direct experience managing clinical studies. (experience)
  • Strong understanding of regulatory requirements, GCP, IVDR, and GDPR. (experience)
  • Experience with BD Biosciences flow cytometry systems and reagents preferred. (experience)
  • Excellent verbal and written communication skills, able to prepare and review complex documents. (experience)
  • Proficiency in MS Office and familiarity with clinical trial databases and flow cytometry software is a plus. (experience)
  • We welcome applications from senior professionals in Clinical Laboratories or Clinical Research Organizations, even if they have no prior industry experience. (experience)

Preferred Qualifications

  • advanced degrees preferred. (degree)
  • Experience with BD Biosciences flow cytometry systems and reagents preferred. (experience)
  • Proficiency in MS Office and familiarity with clinical trial databases and flow cytometry software is a plus. (experience)

Responsibilities

  • Lead clinical trials from planning through completion, ensuring adherence to study timelines and quality standards.
  • Prepare and review key study documents, including protocols, consent forms, investigator brochures, and training materials.
  • Manage relationships with study sites, external laboratories, and service providers, ensuring smooth study conduct.
  • Monitor study progress, budgets, and resources, adapting plans to meet study complexity and milestones.
  • Define and track key study metrics and ensure study data is collected and reported accurately.
  • Conduct site visits as required, oversee staff training, and support study audits.
  • Identify potential risks to study timelines and outcomes and implement mitigation plans.
  • Mentor less experienced team members and support cross-functional collaboration.

Benefits

  • general: A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture.
  • general: You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.
  • general: At BD, you’ll discover a culture in which you can learn, grow and thrive.
  • general: And find satisfaction in doing your part to make the world a better place.
  • general: 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.
  • general: 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.

Travel Requirements

0%

Target Your Resume for "Senior Clinical Project Manager" , Becton Dickinson

Get personalized recommendations to optimize your resume specifically for Senior Clinical Project Manager. Takes only 15 seconds!

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Experience alignment suggestions

Check Your ATS Score for "Senior Clinical Project Manager" , Becton Dickinson

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Tags & Categories

BiosciencesBiosciences

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