Danaher Corporation
External Research & Publications Manager
Danaher Corporation, Brea, California, United States, 92631
External Research & Publications Manager in Brea, California
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. The External Research & Publication Manager for Beckman Coulter Diagnostics is responsible for managing podium and publication activities related to clinical studies as well as external research proposals from the Global Beckman Coulter organization. This position is part of the Clinical Compliance team located in Chaska MN and will be onsite in Chaska or Miami FL. You will report to the Director of Clinical Compliance responsible for research proposals and publications. If you thrive in a fast-paced role and want to work to build a world-class Global Clinical Affairs organization—read on. In this role, you will have the opportunity to: Develop and implement strategies for the dissemination of clinical research findings through podium presentations and peer-reviewed publications. Coordinate with internal and external stakeholders to prepare abstracts, manuscripts, posters, and presentations. Lead and manage the Investigator Sponsored Research (ISR) program, including the review and approval of proposals, budgets, and study protocols. Collaborate with external investigators and internal proposal champions to ensure alignment with company objectives and regulatory requirements. Work closely with cross-functional teams, including Medical Affairs, Regulatory Affairs, and Marketing, to ensure cohesive and strategic communication of research findings. Ensure all ISR and publication activities adhere to Good Clinical Practice (GCP), International Council for Harmonization (ICH) guidelines, and other relevant regulatory standards. The essential requirements of the job include: Bachelor’s degree in a relevant scientific or medical discipline plus 14+ years of experience. Minimum of 5 years of experience in clinical research, with at least 3 years demonstrated experience in managing ISR and scientific communications. Strong understanding of regulatory requirements and industry standards for clinical research and scientific communications. Excellent project management skills, with the ability to manage multiple projects simultaneously. Exceptional written and verbal communication skills, with the ability to present complex scientific information clearly and concisely. It would be a plus if you also possess previous experience in: Advanced degree (PhD, MD, PharmD, or equivalent) preferred. Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology.
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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. The External Research & Publication Manager for Beckman Coulter Diagnostics is responsible for managing podium and publication activities related to clinical studies as well as external research proposals from the Global Beckman Coulter organization. This position is part of the Clinical Compliance team located in Chaska MN and will be onsite in Chaska or Miami FL. You will report to the Director of Clinical Compliance responsible for research proposals and publications. If you thrive in a fast-paced role and want to work to build a world-class Global Clinical Affairs organization—read on. In this role, you will have the opportunity to: Develop and implement strategies for the dissemination of clinical research findings through podium presentations and peer-reviewed publications. Coordinate with internal and external stakeholders to prepare abstracts, manuscripts, posters, and presentations. Lead and manage the Investigator Sponsored Research (ISR) program, including the review and approval of proposals, budgets, and study protocols. Collaborate with external investigators and internal proposal champions to ensure alignment with company objectives and regulatory requirements. Work closely with cross-functional teams, including Medical Affairs, Regulatory Affairs, and Marketing, to ensure cohesive and strategic communication of research findings. Ensure all ISR and publication activities adhere to Good Clinical Practice (GCP), International Council for Harmonization (ICH) guidelines, and other relevant regulatory standards. The essential requirements of the job include: Bachelor’s degree in a relevant scientific or medical discipline plus 14+ years of experience. Minimum of 5 years of experience in clinical research, with at least 3 years demonstrated experience in managing ISR and scientific communications. Strong understanding of regulatory requirements and industry standards for clinical research and scientific communications. Excellent project management skills, with the ability to manage multiple projects simultaneously. Exceptional written and verbal communication skills, with the ability to present complex scientific information clearly and concisely. It would be a plus if you also possess previous experience in: Advanced degree (PhD, MD, PharmD, or equivalent) preferred. Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology.
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