Major Accountabilities

Regulatory Strategy and Implementation

• Supports the diagnostics regulatory strategy for precision IVDs and CDx (e.g. US, EU, Japan, China).

• With support of the RA TA and Diagnostics Lead, responsible for submissions in the premarket as well as post-market space including investigational Device Exemptions (IDE), Significant Risk Determinations, Performance Study Applications (PsA) and pre-market authorization submissions

• With oversight of the RA TA and Diagnostics Lead, works to ensure diagnostic regulatory input for early development and late- stage programs is incorporated into the overall drug development strategy to ensure regulatory requirements pertaining to IVD, CDx and LDT regulations are met

• As needed, partner with RA country organizations to align on local regulatory requirements for precision IVDs and CDx and deliver timely submissions as appropriate including annual reports and notifications

• Facilitates preparation, filing, finalization of briefing books including coordination and planning for pre-Submission or other meetings with HAs related to precision diagnostics and CDx development. Participation in HA meetings as appropriate

• Develops, manages, and implements plans for timely response to HA requests and coordinates of any applicable follow-up activities.

• Member of RA subteam and Biomarker Development Subteam (BDST) as appropriate

Training and Compliance

Support compliance activities for Novartis clinical trials as they relate to global regulations on precision diagnostics and CDx, such as European IVDR Help ensure regulatory compliance of Partner companies for CDx development and IVD deliverables related to our portfolio, as appropriate and elevate to RA Diagnostic Lead where appropriate Support roll-out of new procedures, SOPs and working practices and training related to IVD and CDx development.

Performance Indicators

Successful implementation of regulatory diagnostics strategies with timely submissions for precision IVDs and CDx Full compliance with IVD and LDT rules for our clinical trials Identification of precision IVD and CDx needs for Novartis programs Strong partnership with RA Diagnostics Team members and the RA community Adherence to Novartis Policies and guidelines.

Experiences & Skills

•  Minimum 2-4 years of experience in the pharmaceutical industry with relevant experience related to diagnostics, IVD or CDx development
• Science based BS or MS with requisite experience and demonstrated capability.   Advanced degree (MS, Ph D, PharmD) considered a plus.
• Demonstrated   experience   of successful contributions to a IVD/CDx regulatory project(s) and/or submission
• Experience in the diagnostic, IVD and/or CDx industry
• Understanding of IDE, MAA, NDA/BLA, 510(k), PMA submission(s)
• Understanding of assay validation and CLIA
• Understanding of clinical trials
• Strong interpersonal, communication and negotiation skills

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Commitment to Diversity & Inclusion:

Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve.

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