Clinical Scientist Ultrasound

About the role

Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. 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.

Responsibilities

• 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.
• 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.
• Negotiate and finalize 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.
• Administer 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.
• Execute and monitor clinical trials.
• 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 tools and work with cross-functional teams and tools to ensure payment of milestones and deliverables.
• Maintain oversight of activities at clinical study sites to ensure adherence to GCP, ICH, SOPs, FDA guidelines, study protocols, and internal collaboration controls including compliance.

Qualifications

• Ph.D. or other doctorate degree in Cardiology, Imaging, epidemiology or related disciplines +3 years of relevant experience; master’s degree
• Expertise in Imaging
• Expertise in imaging, cardiology, radiology, procedures
• 5+ years of experience in working with clinical research experience in med tech industry, health care or pharmaceutical.
• At least 4+ years of clinical monitoring experience or clinical trial experience.
• Experience in working with clinical and academic research environments.
• In-depth knowledge of clinical trials and the critical elements for success in clinical trials.
• Knowledge of medical terminology, as well as knowledge of clinical research and scientific principles.

Skills

• Ability to create databases of study variables, organize data, perform statistical analyses, and chart data.
• Demonstrated expertise with Microsoft Word, Excel, database, spreadsheet, PowerPoint, Power BI and analytical software (i.e. SPSS).
• Responsibility to multiple projects and must work both independently and in a team environment.
• Strong customer focus and collaborative.
• Willing & able to travel, as required (up to 60%).

Benefits

• Medical insurance
• Dental insurance
• Vision insurance
• 401(k) retirement plan
• Life insurance
• Long-term and short-term disability insurance
• Paid parking/public transportation
• Paid time off
• Paid sick and safe time

Pay

The Base Pay Range For This Position Is $185,340 - $254,848 Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate.

Schedule

Not specified.