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Senior Director of Medical Safety and Compliance

extra holidays - extra parental leave
Remote: 
Full Remote
Contract: 
Salary: 
300 - 330K yearly
Experience: 
Senior (5-10 years)
Work from: 

Offer summary

Qualifications:

Physician (MD or equivalent), 6+ years of clinical experience, 5+ years leading Medical teams, Bachelor’s degree with 20+ years experience OR Masters/Doctoral degree with 18+ years experience.

Key responsabilities:

  • Lead and manage the Medical Safety Compliance team.
  • Ensure timely medical and clinical consultation for assessments.
  • Manage cross-functional interactions for compliance strategies.
  • Support pre/post-market activities and strategic planning.
  • Represent the company in regulatory discussions.
Beckman Coulter Diagnostics logo
Beckman Coulter Diagnostics XLarge https://www.beckmancoulter.com/
10001 Employees
See more Beckman Coulter Diagnostics offers

Job description

At first glance, you’ll see that for more than 80 years we’ve been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We’re building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and you’ll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful.

Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we’re working at the pace of change to improve patient lives with diagnostic tools that address the world’s biggest health challenges.

The Senior Director of Medical Safety and Compliance will lead the Medical Safety & Compliance team, ensuring that Medical & Scientific Affairs are strategically positioned to provide timely medical and clinical consultation and review for pre- and post-market risk assessments, medical review, and adverse event reporting. This role is crucial in maintaining high standards of medical safety, compliance, and regulatory adherence at Beckman Coulter Diagnostics. Additionally, the role involves significant cross-functional interactions, coordination with quality and regulatory teams, oversight of external safety boards as needed, and a focus on team training, development, and leadership.

This position is part of the Medical and Scientific Affairs team located in US reporting to the Chief Medical Officer and will be a fully remote position. The Medical and Scientific Affairs team strives to provide medical and scientific expertise that drives innovation and clinical adoption of BecDx solutions that improve patient care.

If you thrive in a role utilizing your clinical/medical knowledge helping patients and want to work to build a world-class Medical Affairs organization—read on!

In this role, you will have the opportunity to:

  • Lead and manage the Medical Safety & Compliance team, fostering a culture of excellence and continuous improvement ensuring timely and accurate medical and clinical consultation and review for pre/post-market risk assessments, medical review, and reporting of adverse events.
  • Develop and maintain structures, process and procedure for effective medical risk assessments and all other medical safety activities
  • Manage cross-functional interactions to ensure integration of medical safety and compliance strategies with other departments (quality, regulatory, R&D, and others)
  • Support pre/post-market activities including design specifications, regulatory submissions, and review of marketing and promotional materials.
  • Provide medical/technical input to the strategic planning process for clinical innovation/new product development.
  • Represent the Company in discussions with regulatory agencies about clinical/medical matters relating to existing and future products. 
  • Lead and oversee external expert advisory boards to ensure comprehensive safety and compliance oversight.

The essential requirements of the job include:

  • Physician (MD or equivalent)
  • 6+ years of clinical experience
  • 5+years leading Medical teams
  • Experience with Regulatory Authority presentations is preferred, and strong collaborator.
  • Bachelor’s degree with 20+ years experience OR Masters/Doctoral degree with 18+ years exp.

It would be a plus if you also possess previous experience in:

  • Experience in clinical laboratory operations and/or in vitro diagnostics industries desirable.
  • Board Certification (if US) preferred; Medical specialization preferred
  • Experience or training in adverse event reporting, risk assessments, and/or regulatory submissions desirable.

At Beckman Coulter Diagnostics we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Beckman Coulter Diagnostics can provide.

The salary range for this role is $300K - $330K. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. We may ultimately pay more or less than the posted range. This range may be modified in the future.

This job is also eligible for bonus/incentive pay.

We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.

At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.

Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

The EEO posters are available here.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistance@danaher.com to request accommodation.

Required profile

Experience

Level of experience: Senior (5-10 years)
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Verbal Communication Skills
  • Team Leadership
  • Collaboration
  • Strategic Planning

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