Novartis
Associate Director, Clinical Trial Acceleration
This job is now closed
Job Description
- Req#: 392748BR
Bringing life-changing medicines to millions of people, Novartis sits at the intersection of cutting-edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a diverse learning suite of thousands of programs & an in-house marketplace for rotations & project work. With strong medicines pipeline our current transformation will not just deliver growth for our business but continue to allow us to bring innovative medicines to patients quickly.
Location: The ideal location for this role is East Hanover, NJ site 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 specific NJ site 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 some travel.
About the Role:
Supports the ED/Head, Clinical Sciences, Trial Acceleration and Scientific Alliances with departmental initiatives and the planning, coordination, management, reporting and prioritization of USMA trial acceleration activities.
Key Responsibilities:
•Support Head, Clinical Sciences, Trial Acceleration and Scientific Alliances in the full oversight and management of US trial acceleration activities including facilitate strategic workstreams as required
•Organize key strategic meetings including US Medical Office and others to bring leaders of relevant line functions together to accelerate US trials recruitment, site engagement and satisfaction.
•Develop trackers/dashboards/study profiles for successful monitoring of KPIs related to key US priority trials and research activities
•Support review of trial feasibility results, align with CRMD head and recommend endorsement of allocation proposal of joint GCO/CD/Medical team to TA Head/US CMO
•Partner across functions in the implementation of innovative, transformative, and sustainable solutions to accelerate data generation activities.
•Understand trial acceleration framework and prioritization and assist teams with relevant questions
•Support the development, update and presentation of training materials related to Trial acceleration and Excellence activities.
•Support other clinical sciences, trial acceleration and scientific alliances activities as needed.About the company
At Novartis, we are reimagining medicine to improve and extend people’s lives. We are working hard to produce breakthroughs and address unmet needs for patients with devastating diseases, including genetic disorders and certain deadly cancers. Learn mo...
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