SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Medical Devices organisation, based in Vlaams-Brabant Belgium.

The Company

The client is a subsidiary of a global pharmaceutical company that focuses on the surgical medical devices.

Role Description

You will be responsible for clinical trial management within the Clinical R&D Operations CoE, as well as fostering strong, productive relationships with colleagues across the organization.

Responsibilities

- Serve as a Clinical Trials Manager within the Clinical R&D Operations CoE group to execute company sponsored clinical trials for the Medical Device Franchises
- Manage all operational activities of assigned clinical trials/programs within the Clinical R&D Operations group
- Serves as a member of the clinical trial/study/program core team and may serve as the back-up liaison to the Clinical R&D Franchise and Clinical R&D BSDM for projects/trials/programs under his/her responsibility
- Provide internal communication of important clinical data and events. Functions as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders
- Plan, track and manage assigned projects budgets to ensure adherence to business plans
- Support the implementation of new clinical systems/processes, and provide support for publications, as needed.
- Manage resources assigned to designated clinical studies to provide quality deliverables while maintaining optimal efficiency

Requirements

- Education: Masters or equivalent required. Preferably in Life Science, Nursing or Biological Science.
- Experience: 8 -10 years of relevant experience or equivalent required.
- Minimum of 2 years people management.
- Significant previous experience in clinical project leadership across multiple studies/programs required.
- Experience with budget planning, tracking and control required.
- Relevant industry certifications preferred
- Clinical/medical background a plus.

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Windimi Post.