Clinical Scientist - Structural Heart Disease
Siemens Medical Solutions USA, Inc.

Issaquah, Washington

Posted in Health and Safety

$118.00 per hour


This job has expired.

Job Info


Do you want to join us in helping to fight the world's most threatening diseases and enabling access to care for more people around the world? At Siemens Healthineers, we pioneer breakthroughs in healthcare. For everyone. Everywhere.

At Siemens Healthineers, We offer you a flexible and dynamic environment with opportunities to go beyond your comfort zone in order to grow personally and professionally. Sound interesting? Then come and join our global team as a Clinical Scientist - Structural Heart Disease .

Our global team: We are a team of more than 68,000 highly dedicated employees across more than 70 countries passionately pushing the boundaries of what's possible in healthcare to help improve people's lives around the world. As a leader in the industry, we aspire to create better outcomes and experiences for patients no matter where they live or what health issues they are facing. Our portfolio, spanning from in-vitro and in-vivo diagnostics to image-guided therapy and innovative cancer care, is crucial for clinical decision-making and treatment pathways.

Our culture: We are part of an incredible community of scientists, clinicians, developers, researchers, professionals, and skilled specialists pushing the boundaries of what's possible, to improve people's lives around the world. We embrace a culture of inclusivity in which the power and potential of every individual can be unleashed. We spark ideas that lead to positive impact and continued success. Check our Careers Site at https://www.siemens-healthineers.com/en-us/careers .

The Clinical Scientist - Structural Heart Disease will have responsibility to clinical and academic collaborations within the Cardiology Scientific Division 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 a Clinical Scientist - Structural Heart Disease , 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 tools and work with cross-functional teams and tools to ensure payment of milestones and deliverables.
  • Monitor activities at clinical study sites to ensure adherence to GCP, ICH, SOPs, FDA guidelines, study protocols, and internal collaboration controls including compliance.
Your Qualifications:
  • Ph.D. or M.D. or higher degree in Cardiology, Imaging, or related disciplines.
  • Expertise in structural heart disease, interventional procedures and imaging.
  • 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.
Your Attributes and Skills:
  • Ability to work in a fast-paced industry environment with deadlines and deliverables.
  • 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).
  • Responsible for multiple projects and must work both independently and in a team environment.
  • Detail-oriented with excellent organizational abilities, written and oral communication and presentation skills.
  • Excellent team player with team building skills.
  • Strong customer focus and collaborative.
  • Ability to independently define and meet project requirements.
  • Willing & able to travel, as required (up to 60%).
The pay range for this position is $118,00 - $130,000 annually; however, base pay offered may vary depending on job-related knowledge, skills, and experience. The annual incentive target is 8% of base pay. Siemens Healthineers offers a variety of health and wellness benefits including paid time off and holiday pay. Details regarding our benefits can be found here: https://benefitsatshs.com/index.html .

This information is provided per the required state Equal Pay Act. Base pay information is based on market location. Applicants should apply via Siemens Healthineers external or internal careers site.

At Siemens Healthineers, we value those who dedicate their energy and passion to a greater cause. Our people make us unique as an employer in the med-tech industry. What unites and motivates our global team is the inspiration of our common purpose: To innovate for healthcare, building on our remarkable legacy of pioneering ideas that translate into even better healthcare products and services. We recognize that taking ownership of our work allows both us and the company to grow. We offer you a flexible and dynamic environment and the space to move beyond your comfort zone to grow both personally and professionally.

If you want to join us in transforming the way healthcare is delivered, visit our career site at https://jobs.siemens-healthineers.com/careers

If you wish to find out more about the specific division before applying, please visit: https://usa.healthcare.siemens.com/about .

Beware of Job Scams

Please beware of potentially fraudulent job postings or suspicious recruiting activity by persons that are currently posing as Siemens Healthineers recruiters/employees. These scammers may attempt to collect your confidential personal or financial information. If you are concerned that an offer of employment with Siemens Healthineers might be a scam or that the recruiter is not legitimate, please verify by searching for the posting on the Career site: https://jobs.siemens-healthineers.com/careers

"Successful candidate must be able to work with controlled technology in accordance with US export control law." "It is Siemens Healthineers' policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations."

As an equal-opportunity employer we are happy to consider applications from individuals with disabilities.

Equal Employment Opportunity Statement
Siemens is an Equal Opportunity and Affirmative Action Employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to their race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability unrelated to ability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, gender expression, gender identity, transgender, sex stereotyping, order of protection status, protected veteran or military status, or an unfavorable discharge from military service, and other categories protected by federal, state or local law.

EEO is the Law
Applicants and employees are protected under Federal law from discrimination. To learn more, Click here .

Pay Transparency Non-Discrimination Provision
Siemens follows Executive Order 11246, including the Pay Transparency Nondiscrimination Provision. To learn more, Click here .

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California residents have the right to receive additional notices about their personal information. To learn more, click here .


This job has expired.

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