Summer Intern - Clinical Science

Job description

·  Job facts

In this role, you will review, analyze, and summarize scientific literature and clinical data to generate clinical evidence documentation for compliance with the European Regulation on in vitro diagnostic medical devices (IVDR).

·  Conducts scientific literature reviews, objectively evaluates data, and prepares documentation (eg, scientific validity reports and clinical performance reports) for in vitro diagnostic products.
·  Demonstrates understanding of intended uses of IVDs and their application in clinical practice and applies this understanding to critical review of data and preparation of reports.
·  Ensures high quality documentation with regard to scientific content, organization, clarity, accuracy, format, consistency, and adherence to regulatory and internal guidelines.
·  Works with a cross-functional team (eg, Regulatory Affairs, Development, Medical Office, Quality, Marketing) to ensure timely completion and approval of clinical evidence documentation for Technical Files.

Education/Experience/Skills:

·  Bachelor's in the biomedical or life sciences; Master's, enrolled in PhD or PharmD preferred; oncology experience a plus
·  Experience writing scientific manuscripts, book chapters, review articles
·  Knowledge of literature databases and search methods
·  Excellent verbal and written communication skills
·  Self-motivated, proactive learner

Program Requirements:

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Currently enrolled in an accredited college/university during program calendar year 2020

· 
Completed at least 2 years of college/university to be eligible for the program.

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Must have a ≥3.0 GPA

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Minimum availability of 12 weeks (Required start on or before program Welcome Reception and end date on or after SummerEnd Poster Symposium).

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Previous experience in the job duties listed, either through course work or industry/academia

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Participation in student organizations and/or other leadership experience

What the Intern will Learn:

·  Gain knowledge about requirements of the European In Vitro Diagnostic Regulation (IVDR)
·  Gain knowledge about Ventana's products and how they are used by pathologists
·  Gain experience writing scientific validity and/or clinical performance reports

·  Who we are

Ventana Medical Systems, Inc. (Ventana), a member of the Roche Group, innovates and manufactures instruments and reagents that automate tissue processing and slide staining for cancer diagnostics. Our integrated staining, workflow management and digital pathology solutions optimize laboratory efficiency to reduce errors and support diagnosis for pathology professionals. Together with Roche, Ventana is driving personalized healthcare through accelerated drug discovery and companion diagnostics.

Roche is an equal opportunity employer and strictly prohibits unlawful discrimination based upon an individual's race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other characteristic protected by law.