Danaher Corporation Clinical Project Manager in San Diego, California
Wondering what’s within Beckman Coulter Diagnostics? Take a closer look.
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 Clinical Project Manager for Beckman Coulter Diagnostics is responsible for developing and managing the clinical studies required to validate new immunoassays to support medical decisions relating to Host Response to Infection.
This position is part of the Clinical Affairs Department located in Chaska, MN and remote. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time.
You will be a part of the Clinical Affairs Team and report to the Senior Manager of Clinical Affairs responsible for In-Vitro Diagnostic Clinical Research. If you thrive in an innovative, dynamic role and want to work to build a world-class Clinical organization—read on.
In this role, you will have the opportunity to:
Design and lead clinical research focused on host response to infection including clinical evidence planning and study design.
Develop clinical strategy, protocol design, case report form and informed consent design.
Manage clinical study timelines, resource demand and budget for the project.
Develop internal and external partnerships to ensure stakeholder satisfaction.
Support good clinical practice and scientific integrity concepts.
Proactively identify and resolve business challenges and/or regulatory issues.
The essential requirements of the job include:
Bachelor’s Degree in field with 9+ years of experience or a master’s degree with 7+ years of experience or PhD/MD degree with 4+ years of experience
Experience designing sponsored clinical studies for in vitro diagnostic (IVD), pharmaceutical, or medical device.
Advanced knowledge of Good Clinical Practice and global IVD medical device
Experience developing regulatory strategy as it relates to clinical study design and negotiating with regulatory agencies as a subject matter expert.
It would be a plus if you also possess previous experience in:
Project Managment Professional (PMP)
Experience with Host Response to Infection Research.
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 annual salary range for this role is $120 - $150 K. 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.
When you join us, you’ll also be joining Danaher’s global organization, where 80,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System (https://www.danaher.com/how-we-work/danaher-business-system) tools and the stability of a tested organization.
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 (https://www.dol.gov/agencies/ofccp/posters) .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 firstname.lastname@example.org to request accommodation. If you’ve ever wondered what’s within you, there’s no better time to find out.