Do you want to work for an innovative specialist spinal implant company and play a pivotal role in advancing medical research?
If yes, come to join our clinical studies team as Clinical Project Manager to cover a maternity leave.
9 months fixed term contract
(June 2025- March 2026)
Main Mission:
The Clinical Project Manager is responsible for managing clinical studies on Spineart products from study set up to study closure, ensuring high quality and integrity of data, and compliance with relevant SOPs, regulatory requirements, timelines and within budget.
Your daily responsibilities will include:
- Develops and manages clinical study plan and study budget.
- Coordinates the study protocol and key study document development, and study reports as needed.
- Ensures effective communication of study status to all stakeholders.
- Leads study project team meetings, ensures gaps, risks, actions and decisions documented and communicated.
- Oversees site selection
- Conducts or oversees site initiation, monitoring and site closure and maintains regular and effective communication with sites.
- Ensures quality control of study documents and maintains study quality metrics.
- Trains and oversees monitors (CRAs) and the timeliness and quality of their work.
- Oversees study 3rd party suppliers (CRO, image analysis, others).
Your profile:
- Qualifications within Biological Science, Pharmacy, Medicine or Nursing.
- Minimum 5 years of recent experience as autonomous Clinical Study Manager.
- Clinical study management within medical device industry, class II & III medical devices or spine surgery would be an advantage.
- Very good communication, motivational, organisational skills.
- Fluency in English and French with excellent study document writing skills. Both will be daily working langage.
We look forward to receiving your application at
https://spineart.bamboohr.com/careers/76?source=aWQ9MTE%3D