Job Description
<b>Job Description Summary</b>The ideal location for this role is East Hanover, NJ but remote work may be possible (there may be some restrictions based on legal entity). Please note that this role would not provide relocation as a result. If associate is remote, all home office expenses and any travel/lodging to East Hanover, NJ for periodic live meetings will be at the employee's expense. The expectation of working hours and travel (domestic and/or international) will be defined by the hiring manager. This position will require 10% travel.The Vendor Program Strategy Director (VPSD) acts as the Business Partner for all vendor activities with the Clinical Operational Program Head (COPH). The VPSD, in collaboration with the COPH, Portfolio Innovation Director (PID), the ERMT and Procurement defines the program vendor strategy end-to-end. The VPSD is accountable at program level for the vendor delivery across the clinical study lifecycle from study start-up, recruitment, maintenance and closeout in accordance with GCP, ICH, SOP's, and regulations#LI-HybrdKey Responsibilities:<br>End-to-end accountability for all supplier related activities at a program level across GDD Portfolio<br>Manages a program view of supplier performance relative to the defined strategy<br>Defines and aligns program strategies in close collaboration with Alliance Lead, ERMT, PID and Procurement<br>In collaboration with Vendor Alliance Leads, reviews geographic scope of global vendors and drives local vendor service delivery discussions with country representatives in case of gaps<br>Understands upcoming portfolio demand within Program through COPH role (new trials, new program, BR transition, BD&L, research collaboration) and pushes information to Vendor organization<br>Understands and translates new service needs, in advance, and engages with Vendor Alliance Lead for vendors to be identified, qualified, and contracted to support future Programs/Trials<br>Engages with Head Vendor Alliances to understand the latest in category strategy, supplier performance, supplier innovation <br>Enables early engagement with suppliers during protocol development & feasibility stage<br> <b>Job Description</b><b>Essential Requirements:</b><ul><li>Advanced degree in science or business with equivalent experience Strongly Preferred</li><li>10+ years relevant industry experience, including expertise in clinical operations leadership of multidisciplinary teams, experience management outsourced trial activities at an operational and strategic level Strongly Preferred.</li><li>Demonstrated executive leadership in developing and managing external and internal strategic relationships</li><li>Experience with clinical processes and associated supplier services, with excellent understanding of trial management, trial monitoring and overall integration of clinical data system and processes</li><li>Strong technical and problem solving skills Excellent understanding of clinical trial methodology, GCP and medical terminology</li><li>Excellent understanding of clinical development, quality & regulatory standards and policies relevant to defined services</li></ul>Novartis Compensation and Benefit Summary: The pay range for this position at commencement of employment is expected to be between $176,400 and $327,600/year; however, while salary ranges are effective from 1/1/25 through 12/31/25, fluctuations in the job market may necessitate adjustments to pay ranges during this period. Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills, and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as