Expert Global trial manger

322828BR
Jul 07, 2021
India

Job Description

With over 400 active trials in 5 hub countries, Novartis GDO Trial Management is committed to delivering end-to-end support to make the clinical trial process more efficient and patient-friendly. We bring together and manage all aspects of clinical trial operations to meet milestones in terms of quality, cost, and delivery time in order to better serve our patients. We develop strategies to optimally deploy resources as well as manage performance, budgets, and contractors. TM is a proactive learning organization focused on collaboration and individual development to foster a synergistic environment. We rise to meet the challenges of the future by utilizing the latest digital technologies and data while optimizing risk 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 patients.

Your responsibilities include, but are not limited to:

• Contributes, with appropriate oversight, to all aspects of global clinical trial(s) to deliver study outcomes within schedule, budget, quality/compliance and performance standards.
• May lead specific aspects of global clinical trial(s). Core member of the Clinical Trial Team, Contributes to operational excellence through process improvement and knowledge sharing
• Contributes to all operational trial deliverables, according to timelines, budget, operational procedures, and quality /compliance and performance standards.
• Conduct study start -up activities such as overseeing protocol development, CRF development, Informed Consent Form development.
• May identify new sites for clinical trials; analyze capability and make recommendation for trial inclusion.
• Ensuring proper handling of all study close out activities including but not limited to site close out, final drug accountability and audit readiness of Trial Master File documentation.
• Responsible for education, implementation and compliance to standards (SOPs) and best practices for clinical operations within assigned clinical trial(s) and within clinical program(s), including sharing lessons learned.

Minimum Requirements

• Timely, efficient and quality execution of assigned trials and trial related activities within budget, and in compliance with quality standards.
• Proactive operational planning with effective contingency and risk mitigation plans.
• Adherence to Novartis policy and guidelines and external regulations
• Operations Management and Execution
• Project Management Financial Management
• Collaborating across boundaries

WHY NOVARTIS
769 million lives were touched by Novartis medicines in 2020, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives.
We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working.
We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!
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.
Join our Novartis Network : If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network
Global Drug Development
GDO GDD
India
Hyderabad, AP
Research & Development
Full Time
Regular
No
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322828BR

Expert Global trial manger

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