Senior Clinical Project Manager
Nestlé
Switzerland-VD-Lausanne
vor 4 Tg.

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Job Description - (18000140)

Job Description

Senior Clinical Project Manager(

Job Number : 18000140)

Description

Senior Clinical Project Manager More people who think like you and less who think like everyone else Nestlé Research Center, Lausanne, Switzerland Undefined period of time contract, act rate 100% Over the last 5 years, the 600-

staff NRC has published around 1000 scientific publications in peer review journals and files about 80 patents every year.

The NRC also has around 100 research collaborations with universities or research institutes around the world. The NRC is organized with three large research institutes for Nutritional Science, Materials Science and Food Safety & Analytical Science.

Research Units focusing on Clinical Development, and PetCare, complement these major Institutes. The NRC plays an important role in providing the science behind healthier products (learn more about the NRC at www.

research.nestle.com). The Clinical Development Unit provides the expertise, resources and facilities to design clinical studies and execute these throughout the work.

Yet, a successful clinical journey, leading to meaningful scientific evidence, is impossible without tight teamwork between Nestlé business partner, internal R&D entities, research sites and service providers.

The CDU is committed to apply flexible and tailored approaches, while complying with regulatory, ethical requirements and quality standards.

Demonstrating result focus and strong initiative , you will be fully accountable for all operational and strategic aspects of study conduct, for the flawless, efficient and smooth execution of the Clinical trial while complying with internal Standard Operating Procedures, applicable laws and ICH Good Clinical Practice.

Manages high complex or high risk end-to-end clinical trials and broad knowledge in operations, R&D and business. Key responsibilities

  • Provides critical reviews and inputs of clinical operational aspects for development of Clinical Substantiation
  • Provides realistic timelines, states practical and valid operational models
  • Provides strategic and tactical guidance in risk management taking into account the business interests
  • Identification of project and clinical trial risks and the development and implementation of the mitigations for these risks
  • Contributes to the study protocol outline, study set up
  • Assesses & pronounces on clinical site(s) & staff's suitability to conduct the protocol.
  • Secures stakeholders agreement with the assessment outcomes.
  • Take daily decisions in the best interest of the business and supervises the CPM responsible of the day to day operations if applicable.
  • Ensures that the trial is progressing according to Clinical Development Unit (CDU) quality standards
  • Manages the risks and recommend corrective actions to improve efficiency and remove obstacles.
  • Reporting on budget to concerned SBU or business Project Manager.
  • Acts as Single Point of contact and bridge between the Business and CDU to maintain efficient communication flow on both sides
  • Contributes to the strategy of the Clinical Management Group by identifying areas of improvement for increasing efficiency, innovations
  • Required profile

  • Minimum of 7+ years clinical project management experience in Food / Pharma / CRO industry
  • Proven experience in leading & coordinating the activities of cross-functional operational teams and communication with internal & external trial stakeholders
  • Experience of working with clinical sites to execute protocols
  • Experience of risk assessment, implementation of mitigation plans and continuous review and adjust to plans as required
  • Co-ordination of investigational product preparation, logistics and management of supply throughout trial as well as management of biological sample logistics
  • Preparing and / or reviewing essential trial documents, maintenance of Trial Master Files and managing EC approval process
  • Training and supervision of junior colleague's work
  • Fluent in English, other European languages will be considered an asset
  • Show us that you have a creative and collaborative mindset and you are able to propose new and innovative ideas. Your strong interpersonal skills with the ability to build and enhance relationships with CRO study teams is what will set you apart among the other candidates.

    Your flexibility to handle a variety of tasks and shift priorities as necessary and your ability to work as an effective team member in a virtual environment will contribute to your and our success.

    If you are dedicated to apply scientific knowledge and demonstrate an excellent scientific communication, and you want to make a difference to our performance, please apply in English at : The Nestlé Group is the world’s largest food and beverage company with 89,5 billion Swiss Francs in sales in 2016.

    It is present in 191 countries around the world, has 418 factories and its 328,000 employees are committed to Nestlé’s purpose of enhancing quality of life and contributing to a healthier future.

    Nestlé offers a wide portfolio of products and services for people and their pets throughout their lives. Its more than 2000 brands range from global icons like Nescafé or Nespresso to local favourites.

    Company performance is driven by its Nutrition, Health and Wellness strategy. Nestlé is based in the Swiss town of Vevey where it was founded more than 150 years ago.

    Learn more about our Group and reasons to join us on .

    Job Posting

    Feb 12, 2018, 7 : 59 : 26 AM

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