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Global Study Manager - Geneva
View: 161
Update day: 26-03-2024
Category: R & D IT - Software
Industry: Biotechnology Hospital & Health Care Pharmaceuticals
Position: Associate
Job type: Full-time
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Job content
Job DescriptionJob Overview:
- Are you an experienced Project Manager looking for your next challenge?
- Do you want to work for a global organisation with un-paralleled career development opportunities?
- Do you want to work for a company that helps build a healthier and safer world?
Job Responsibilities Include
As a key member of the Project Management department, you will be managing a portfolio of global, high complexity clinical studies. As such, your main responsibilities will entail:
- Being the key contact between our clients (pharmaceutical companies), the various departments within our Central Laboratory organization, other Covance business units and external vendors
- Providing project management oversight for your portfolio of studies, focusing on key client deliverables through budget, risk, and milestone management
- Ensuring successful interactions between the clients and the extended Covance study management team you are collaborating with (e.g. Study Design Lead and Regional Study Coordinators)
- Reviewing the study protocol to ensure quality implementation and successful delivery of client specifics and requirements
- Being accountable for the implementation, monitoring and reporting of performance metrics
- Ensuring that all customer expectations are documented and acted upon in compliance with regulatory requirements
- Working with appropriate internal and external personnel to understand the culture and pipeline of assigned clients
- A strong and experienced project management team who will contribute to and support your personal and professional development
- A competitive salary together with a comprehensive benefits package including health and pension
- Unsurpassed career development opportunities supported by exceptional people from across the globe with an energizing purpose
BSc or Master degree in life science or equivalent
Experience
- 2- 5 years’ experience in managing projects in pharma industry or in a CRO, preferably in clinical trials.
- Demonstrated leadership skills
- Proven ability to negotiate and collaborate to deliver effectively
- Great customer service skills
- Ability to make difficult decisions and act efficiently in an environment with dynamic timelines
- Dedicated to a culture of quality and continuous improvement
- Strong communication skills
- Fluent in English
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Deadline: 10-05-2024
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