SPINEART is a privately held medical device company based in Geneva, Switzerland, focused on simplifying the surgical act by designing, developing, and promoting safe and efficient solutions to spine surgeons, operating room teams, and patients.

Selling in over 60 countries, Spineart is a pioneer in its field, having introduced unique technologies in the fields of Minimally Invasive Surgery, Motion Preservation, Fusion, Biologics and Fracture Treatment.

Spineart markets a complete portfolio combining traceable barcoded sterile packed implants with compact instrument sets, thus proudly promoting greater safety, cost-efficiency, and compliance at the hospital.

Our success also depends on our team’s value. The human being is at the centre of our concerns. We pay special attention to our recruitment to make Spineart a great place to work.

For us, soft skills are as important as hard skills. What we expect from our employees is nothing short of real team spirit, mutual assistance, and self-transcendence.

Our philosophy: Quality, Innovation, Simplicity

Our values: Respect, Integrity, Solution oriented

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.

8 months fixed term contract

(August 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

Job Types: 100%, Fixed term
Contract length: 8 months

Schedule:

• Day shift
• Monday to Friday

Work Location: Hybrid remote in 1228 Plan-les-Ouates, GE

Expected Start Date: 02/06/2025