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Global Trial Manager
View: 262
Update day: 26-03-2024
Location: Boudry Neuchâtel NE
Category: R & D IT - Software
Industry: Pharmaceuticals
Position: Associate
Job type: Full-time
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Job content
At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.Responsibilities involve a combination of execution and oversight, dependent on the sourcing model, to ensure deliverables and may include, but are not limited to, the following
Project Management
- Drives study execution utilizing available performance metrics and quality indicators (e.g. CTMS, eTMF reports, RBM reports), and study milestones and drivers.
- Develops, manages, and maintains study deliverables (i.e. timelines, study plans, etc.) through collaboration with internal and external stakeholders using data and strong interpersonal influencing skills to make robust data driven decisions.
- Insourced Studies Provides strategic input into Study Team – e.g., on study documents.
- Outsourced Studies Reviews/approves functional plans; Provides information to the CRO and reviews CRO deliverables.
- Proactively develops/maintains collaborative relationships with internal partners/stakeholders across the multidisciplinary teams.
- Creates realistic plans that clearly define goals, milestones, responsibilities, and results.
- Maintains focus on strategic objectives while accomplishing operational goals.
Experience Requirements
- Minimum 4 years of demonstrated project management experience of which at least 2 should have been in the pharmaceutical or healthcare industry.
- Experience in leading global clinical trials and multi-functional teams.
- Demonstrated project management and organizational skills with strong presentation and communication abilities.
- Experience with electronic quality, compliance and CTMS systems. Experience in managing CROs is a plus.
- Risk management experience preferred.
- Clinical trial project management skills
- Financial budgeting and forecasting skills are a plus.
- In depth knowledge of ICH/GCP, regulatory guidelines/directives, and drug development and clinical research processes.
- Proven success in using oral/written communication skills to influence, inform, or guide others.
- Computer skills - Microsoft applications including (but not limited to), Word and Excel and PowerPoint
- Proficiency in study tools including electronic system skills – e.g. CTMS/eTMF.
- Understands interdependencies, links possible solutions, and escalates issues with proposed solutions to appropriate people.
- Reacts with a sense of urgency and responds appropriately.
- Critical thinking skills for problem solving and the lateral and strategic thinking capacity to drive the study(ies).
- Adaptable and flexible—willing/able to adjust to multiple demands and shifting priorities
- Ability to effectively lead a cross-functional team in a matrix environment.
- Fosters a continuous learning mindset.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.
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Deadline: 10-05-2024
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