Associate Global Trial Director

329155BR
Oct 06, 2021
USA

Job Description

With over 400 active trials in 5 hub countries, Novartis GDO Trial Management feels privileged to bring together and manage all aspects of clinical trial operations reaching around 50 000 patients worldwide.

We are a proactive learning organization and we place a lot of emphasis on collaboration and individual development. As part of this we are very committed to evaluating the latest digital technologies, always looking to transform trials and improve lives.

TM is in search of those who are passionate about applying their experience to reimagine clinical trial operations and ultimately improve the lives of our team, our organization and our patients.
We are Novartis. Join us and help us reimagine medicine.

As the leader of the cross-functional clinical trial team, leads planning and management of the assigned clinical trials end-to-end to achieve Oncology Medical Affairs (OMA), Global Medical Affairs (GMA), GMA Franchise, Global Clinical Team (GCT) and Clinical Trial Team (CTT) objectives. Oversight of budget and resource allocation within assigned trial. Drives operational excellence through process improvement and knowledge sharing across trials within disease area. Enables an empowered organization that can navigate in a matrix environment and adjust quickly to business needs. Point of escalation for resolution of trial management operational issues within assigned trial(s)

1. Lead and manage the global cross-functional CTT to ensure deliverables are met within the established timelines, budget and quality/compliance standards; accountable for representation at all internal meetings related to clinical trials; chair the routine CTT meetings, report study progress and issues/resolution plan at the Global Clinical Team (GCT). Core member of the GCT.
2. Lead the development of global clinical trial protocol(s) by translating the approved trial concept sheet(s) into efficient, high quality, executable clinical protocols: • Responsible for integrating and authoring clinical trial protocol(s) and related documents (e.g. informed consent) in collaboration with the Global Medical Director, the CTT members and the Novartis Country Pharma Organizations (CPOs) • Submit clinical trial protocol(s) to internal review board for approval; • Lead the development of scientific trial related documents (e.g. charters, scientific training material) with input of the of the Global Medical Director, and other line functions (e.g. data management, statistical analysis, etc.) as needed • Organize and participate in trial advisory committees (e.g. Data Monitoring Committee, Steering Committee). • Collaborate with the Global Medical Directors and Advisors of the major Novartis local medical organizations to ensure country feedback is adequately integrated into protocol.
3. Trial planning, execution and close-out: • Ensure trial feasibility and site selection process. Where applicable in collaboration with Trial Monitoring organization. • Ensure all required documentation is provided to each participating country for Health Authority (HA) and/or Institutional Review Board (IRB)/Institutional Ethics Committee (IEC) submissions •
Conduct investigator meetings/trainings in collaboration with the Novartis CPOs. Provide study specific training for Novartis CPOs and Regions

Diversity & Inclusion / EEO

The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.

Minimum Requirements

The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.
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Global Drug Development
GDO GDD
USA
East Hanover, NJ
Research & Development
Full Time
Regular
No
329155BR

Associate Global Trial Director

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