Expert Clinical Manager (CM) - NOVJP00026340 (m/f)

Basel  ‐ Onsite
This project has been archived and is not accepting more applications.
Browse open projects on our job board.

Description


  • You will work in one of the biggest and most successful pharmaceutical companies worldwide
  • You will work at the Headquarter on the Novartis Campus in Basel
  • Novartis' strategy is to use science-based innovation to deliver better patient outcomes in growing areas of healthcare

Expert Clinical Manager (CM) - NOVJP (m/f)

Reference: -en
Start: 06/18
Duration: 12 MM++

Main tasks:
  • Contribute to all operational trial deliverables, under the oversight of the (Associate) Global Trial Director, according to timelines, budget, operational procedures, quality /compliance and performance standards
  • Support the Global Trial Director with the development, management and tracking of the trial level life cycle budget incl forecast, and annual cost targets
  • Core member of the global cross-functional Clinical Trial Team (CTT); participate and report study progress and issues/resolution plan at the CTT meeting; write CTT meeting minutes; can deputize for the (Associate) Global Trial Director to chair and facilitate CTT meetings. Organize and chair trial sub teams within the scope of his/her delegated responsibilities. Extended member of the Global Clinical Team (GCT)
  • As member of the CTT, contribute to defining the data review plan; participate in data review as specified in the Data Review Plan
  • Contribute to talent development through active participation in onboarding and training activities. May participate in GDO Trial
  • Management initiatives and working groups
  • Responsible for education, implementation and compliance to standards (SOPs) and best practices for trial management within assigned clinical trial(s) and within clinical program(s) and franchise, including sharing lessons learned


Main qualifications
  • Involvement in cross-functional, multicultural and international clinical trials; demonstrated capabilities in supporting operational aspects of clinical trial related activities
  • Excellent communication, organization and tracking skills. Strong operational skills and demonstrated ability to meet timelines
  • Proven ability to work either independently or in a team setting, to meet goals by managing compliance, budget and timelines
  • Proven networking skills and ability to share knowledge and experience amongst colleagues
  • Knowledge of Good Clinical Practice; comprehensive knowledge of clinical trial design; understanding of the overall drug development process
  • Basic knowledge of appropriate therapeutic area


Main advantages:
  • May lead specific aspects of global clinical trial(s)
  • Core member of the Clinical Trial Team, deputy for the (Associate) Global Trial Director
  • Contributes to operational excellence through process improvement and knowledge sharing
  • Gaining work experience in one of the biggest pharmaceutical companies worldwide



About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
Start date
06/18
Duration
12 MM++
(extension possible)
From
Hays AG
Published at
19.05.2018
Contact person:
Kerstin Werner
Project ID:
1557804
Contract type
Freelance
To apply to this project you must log in.
Register