Clinical Project Manager

Clinical Project Manager

Nestle

Lausanne, Switzerland

To complete our Clinical Operations team, we are currently looking for a Clinical Project Manager. In this role, you will 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.

Key responsibilities

  • Provide critical reviews and inputs of clinical operational aspects for development of Clinical Substantiation Plan and Protocol Outline;
  • Contribute to the study and/or site budget development, protocol outline development (i.e. ensure operational aspects are realistic and feasible) Case Report Form development and Informed Consent Form template development;
  • Assess & pronounce on clinical site(s) & staff's suitability to conduct the protocol;
  • Supervise the Core Team (CRO) responsible of the day to day operations by leading & coordinating the activities of cross-functional operational teams and communication with internal & external trial stakeholders;
  • Monitor the big picture dynamics influencing the project progress, manages the risks and recommend corrective actions to improve efficiency and remove obstacles;
  • Track & manage study contracts to provide timely and accurate forecast into financial management systems and so delivering study to agreed budget;
  • Ensure alignment between the Clinical Development Lead and Clinical Trial Team by acting as Single Point of contact and bridge between the Business, the CRO, the Clinical Development Lead to maintain efficient communication flow;
  • Contribute to the strategy of the Clinical Operations Group by identifying areas of improvement for increasing efficiency, innovations (Clinical research beyond the traditional approach, external alliances…).

Required Profile

  • Confirmed experience in Pharma/CRO industry with at least 7 years’ background in Clinical Project Management;
  • Exposure to risk assessment, implementation of mitigation plans and continuous review and adjust plans as required;
  • Ability to manage and coach CRAs and other clinical trial personnel, as well as training and supervision of Junior colleague’s work;
  • Capable to manage budget and contracts;
  • Fluent in written and spoken English, French or any other language is required.

Show us that you are capable to manage Clinical Trials from end to end. Your clinical research organizational and negotiating skills are important. Your entrepreneur mindset and your convincing skills is what set you apart from other candidates.

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© EuroJobsites 2019

EuroJobsites is a UK registered company number: 4694396 VAT number: GB 880 9055 04

Registered address: EuroJobsites Ltd, Unit 8, Kingsmill Business Park, Kingston Upon Thames, London, KT1 3GZ, United Kingdom

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