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Medical Director

Remote: 
Full Remote
Contract: 
Salary: 
265 - 285K yearly
Experience: 
Mid-level (2-5 years)
Work from: 

Offer summary

Qualifications:

Physician or Board-certified Clinical Pathologist, 3+ years of clinical/laboratory experience in Hematology, Chemistry, Immunoassays, Strong presentation skills and collaboration.

Key responsabilities:

  • Provide medical consultation for risk assessments.
  • Review and update risk assessment documents.
  • Support pre/post-market regulatory activities.
  • Represent the company in regulatory discussions.
  • Assist in training for consultants and internal teams.
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Molecular Devices Biotech: Biology + Technology Large https://www.moleculardevices.com/
1001 - 5000 Employees
See more Molecular Devices 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 Medical Director, Scientific and Medical Affairs position for Beckman Coulter Diagnostics is responsible for partnering with business stakeholders in the laboratory diagnostics community and providing medical/clinical input into Safety, New product development and pre/post-market risk management.

This position is part of the Medical and Scientific Affairs team located in US 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.

You will be a part of the Medical and Scientific Affairs team and report to the Senior Director, Medical and Scientific Affairs. 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:

  • Provide and ensure timely medical and clinical consultation and review for pre/post-market risk assessments, medical review, and reporting of adverse events.
  • Review and comment on medical risk assessments for complaints; sign-off on reportability of Medical Device Reports (MDR)
  • Review, update and create risk assessment documents related to potential product specific malfunctions
  • Identify and report any quality or compliance concerns and provide clinical input and support to taking immediate corrective action as needed.
  • 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.
  • Assist in the planning and provision of training for external medical/scientific consultants, speakers and internal teams as needed.

·        

The essential requirements of the job include:

  • Physician Or Board-certified Clinical Pathologist, Or Clinical/Anatomic Pathologist (by training or education) with relevant professional experience.
  • 3+ years of clinical/laboratory experience in Hematology, Chemistry, and Immunoassays post training.
  • Demonstrated presentation skills to multiple audiences, and strong collaborator.

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

  • Experience in clinical laboratory operations and/or in vitro diagnostics industries desirable.
  • 2+ years of practice or industry experience post training.
  • 2+ years of clinical/laboratory experience in Flow Cytometry post training.
  • Experience in clinical laboratory operations and/or in vitro diagnostics industries desirable.
  • 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 $265K - $285K. 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: Mid-level (2-5 years)
Industry :
Biotech: Biology + Technology
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Collaboration

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