Clinical Scientist Ultrasound

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We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions.

Facilitates and develops the relationship with the medical/scientific community including physicians and medical centers.

TheClinical Science Liaison will have responsibility to clinical and academic collaborations within the Clinical Science and Collaborations segment of the Ultrasound Organization.Research is focused upon driving evidence generation from collaborations, clinical trials, and enhancing partnerships with external key thought leaders and luminaries.

This is a role well suited to an ambitious professional, looking for the next step in their career.

As aClinical Science Liaison, you will be responsible for:

Research and Development:



* Scientific expertise for developing research collaborations.


* Remain current with published literature and clinical results for strategic purposes.


* Promote continuous dialogue with collaborators to identify opportunities for collaboration on research topics and to translate these into project proposals.


* Provide scientific feedback and advice to internal and external partners regarding our technologies.


* Work directly with collaboration partners and research staff at luminary academic institutes.


* Compile data and write project results, while performing statistical analysis and using statistics to develop study endpoints, sample size, etc.


* Provide oversight of investigator-initiated research studies.

Collaboration Management:



* Contribute to study development and start-up process including reviewing protocols, drafting of IRB packages, consent forms, designing and/or reviewing CRFs, writing collaboration contracts, executing collaboration contracts, preparing volunteer Informed Consent forms, developing study documents, organizing, and presenting at investigator meetings, while working with management on monitoring strategy.


* Negotiating and finalizing contracts for execution with support from legal, regulatory and compliance.


* Ensure that all study related documents are tracked, filed and reviewed, and complete according to SOPs, regulatory requirements and protocol.


* Administrative and logistical tasks, including tracking, collecting, distributing, and filing study documentation.


* Ensure collaborations are on track for site initiation, subject recruitment and enrollment, as well as close-out.


* Clinical trial execution and monitoring.


* Work with management team to define timelines of milestones, deliverables and data.


* Design reports and metrics that are useful management tools for projects.


* Adapt to collaboration archiving to...