A career is an ongoing journey of discovery: our 51,000 people are shaping how the world lives, works and plays through next generation advancements in healthcare, life science and performance materials. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others.
Would you like to be at the forefront of making amazing things happen for patients all over the world?
The Principal Clinical Research Manager role we have available at our company is an enviable position within which an individual can lead and impact some of the most important clinical studies taking place for our patients both now an in the future.
In the Principle CRM role, you will be accountable for all aspects for the management of local and/or regional company sponsored studies, as well as Global Phase IV studies, including study plans, timelines, resources, allocation and management of product (re-) supply, problem identification and resolution, status reports and budget to ensure timely delivery of completed study reports to the project teams .
You will be accountable for the oversight of IST/ISS granted by the company, including the support of the set-up and operational assessment of investigator-sponsor, tracking performance and payments according approved plan, managing product supply, if applicable, coordinating internal review of final report
You will manage independent consultants including CROs, clinicians, independent CRAs, or statisticians when required by the project including selection, coordination of project specific training, and payment.
You may be responsible for performance management of the assigned team.
You will provide an interface with the local Medical Affairs organization and ensuring alignment on trial strategy.
Who you are:
- a Medical and/or Life Sciences degree, with extensive experience in clinical research in a CRO, pharma or biotech company, preferably in a managerial position
- Good country-specific knowledge and experience in clinical trial management and conduct
- Good knowledge of ICH GCP and applicable local regulations and requirements
- Demonstrated good organizational ability: time management, prioritization, able to handle and oversee multiple tasks simultaneously, demonstrated good interpersonal skills including good people management skills
- Fluency in English (oral and written)
We are a company committed to investing in and developing our employees, the career prospects within this role are quite broad and will depend on the individual’s aspirations and their desire to challenge themselves.
What we offer: We empower you to fulfil your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life!
Curious? Apply and find more information at https://jobs.vibrantm.com