Position Summary This Clinical Specialist I is an entry-level position within STERIS Procedural GI’s Clinical team that focuses on new product efforts, which may include sourced, acquired or internally developed products…
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$80k–$103k/yr
Full-time
bachelor degree
Paid Time Off, Healthcare, Dental, Vision, Long Term Disability, Short Term Disability
Posted 26d ago
~40 hrs/week
Responsibilities
Provide clinical expertise and collect Voice of Customer feedback to support the development and validation of new GI Endoscopy products. Collaborate with cross-functional teams to ensure patient safety and clinical accuracy in product design and marketing materials.
Requirements
Requires a Bachelor's degree and a Registered Nurse certification with at least 5 years of hands-on GI endoscopy experience. Must have experience assisting in therapeutic endoscopy procedures and the ability to travel 10-20%.
Full job description
Position Summary
This Clinical Specialist I is an entry-level position within STERIS Procedural GI’s Clinical team that focuses on new product efforts, which may include sourced, acquired or internally developed products. This individual will provide clinical expertise, support market research in the form of Voice of Customer and execute product evaluation activities for new products. The Clinical Specialist I will become familiar with the process of New Product Development, as well as for Third Party product introductions and contribute deliverables as required under FDA Design Controls or otherwise. Prototype validation testing with the use of simulated models is a key function of this role. This position is cross functional in nature and the individual must be able to work on teams with a variety of business functions, keeping patient safety and clinical outcomes at the forefront of many decisions.
Location: Greater Cleveland, OH area
Work model: Hybrid, this position will require time working in the Mentor, OH office. Typically 2–3 days onsite (Tue–Thu preferred)
Travel: Approximately 10-20% travel required
What You'll do as a Clinical Specialist
Collects Voice of Customer feedback from doctors and nurses within the GI Endoscopy field regarding existing and new product development projects. Voice of Customer can include feedback on prototypes, explanation of user needs relative to a particular device or procedure, competitive device preferences, etc. It can be gathered in person, virtually, through conferences, literature, etc. Presents the Voice of Customer collected and provides clinical and patient-centered input to assigned Cross Functional Team.
Collaborates with multiple functional roles throughout the product development process, providing Clinical perspective and personal expertise in GI Endoscopy, until the product is released to the market for sale.
Exhibits working knowledge of both the various product development processes and FDA Design Controls relevant to this role.
Supports projects throughout the Stage Gate process by providing clinical input and deliverables (such as contributions to Risk Analysis (DFMEAs), development of Instructions for Use, contributions to Clinical Evaluation Reports and Literature Search Reports, Design Validation Plans, etc., as needed.
Conducts verification testing on new products and competitive products.
Supports Hands-On Workshops and Key Opinion Leader development initiatives to support commercial training and acceptance of products.
Delivers Contact Hour presentations to provide CE credits.
Reviews and contributes to marketing collateral (brochures, videos, quick reference guides, article summaries, etc.) for clinical accuracy.
Provides general endoscopy support and education, as needed.
The Experience, Skills and Abilities Needed
Required
Bachelor’s Degree required
Registered Nurse with minimum of 5 years hands on GI endoscopy experience
Ability to travel
Preferred
Hands on experience assisting in Therapeutic Endoscopy procedures
Surgical or pulmonary experience is desireable
Skills
Decision making
Solution-oriented and collaborative
Positive attitude
Excellent oral and written communications skills
Ability to multitask
Ability to work within a cross functional team and consider multiple viewpoints
Basic computer skills (Microsoft Office, online literature searches)
What STERIS Offers
We value our employees and are committed to providing a comprehensive benefits package that supports your health, well-being and financial future.
Here is a brief overview of what we offer:
Market Competitive Pay
Extensive Paid Time Off and (9) added Holidays
Excellent Healthcare, Dental and Vision Benefits
Long/Short Term Disability Coverage
401(k) with a company match
Maternity and Paternity Leave
Additional add-on benefits/discounts for programs such as Pet Insurance
Tuition Reimbursement and continued education programs
Excellent opportunities for advancement in a stable long-term career
#LI-SA2
#ZRSA-1
#LI-Hybrid
Pay range for this opportunity is $79,687.50 - $103,125.00. This position is eligible for bonus participation.
Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc.
STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: STERIS Benefits
Open until position is filled.
STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare and life sciences products and services around the globe. For more information, visit www.steris.com.
If you need assistance completing the application process, please call 1 (440) 392.7047. This contact information is for accommodation inquiries only and cannot be used to check application status.
STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.
The full affirmative action program, absent the data metrics required by § 60-741.44(k), shall be available to all employees and applicants for employment for inspection upon request. The program may be obtained at your location’s HR Office during normal business hours.
Related keywords
GI EndoscopyFDA Design ControlsVoice Of CustomerNew Product DevelopmentDFMEAClinical Evaluation ReportsDesign ValidationTherapeutic EndoscopyPrototype ValidationStage Gate ProcessInstructions For UseMedical DevicesPatient SafetyClinical OutcomesBench TestingAnimal Lab Testing
US Endoscopy is a new product development company, focusing on device design and manufacturing in the gastrointestinal endoscopy and urology markets. With the guidance and direction of luminary physicians and nurses worldwide, US Endoscopy focuses on the most urgently needed solutions, ultimately providing better, more enhanced product options for clinicians. US Endoscopy was founded in 1991, with headquarters in Mentor, Ohio. For more information on US Endoscopy, visit www.usendoscopy.com.
Offices: 5976 Heisley Road, Mentor, OH 44060, US
medical device manufacturingElectronicsHealth CareHardwareManufacturing
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