Clinical Specialist (Medical Device)

TurkuCompetitiveHybrid0 applicants

About this role

Bonalive Oy

As the world seeks answers to the growing threat of antibiotic resistance, Bonalive represents a new standard in patient care. Evolving at the intersection of technology and human biology, our Smart Healing™ technologies reduce antibiotic treatments and enable a better quality of life for patients. Smart Healing™ encompasses our commitment to our customers. It defines everything we do, in providing patients and surgeons well-proven and safe bone regenerative products in orthopedics, trauma, spine, septic bone and ear surgery. Bonalive is a smart biomaterials company transforming the future of healthcare. With one of the most evidence-based technologies in the industry, we are creating a smarter future for healthcare. Bonalive is an ISO 13485:2016 certified, Class III medical device company, headquartered in Turku, Finland. www.bonalive.com

Clinical Specialist

Turku, Finland

We are looking for a Clinical Specialist to strengthen Bonalive’s clinical and scientific support capabilities in an international and growing medical device environment.

The role combines clinical affairs work, scientific support and clinical project coordination to support the safe and effective use of Bonalive products. The position works closely with QA/RA, Commercial, MC&E, R&D, distributors, healthcare professionals and clinical partners globally.

The position is primarily based at Bonalive’s Turku headquarters.

During the onboarding phase, work is carried out on-site.  After that, hybrid work is possible (up to 2 days per week).

Key responsibilities:

Support indication managers in validating clinical claims

Review clinical literature and support literature searches

Identify clinical evidence gaps together with internal stakeholders

Support evidence-based communication and scientific messaging

Compile and support clinical case reports and clinical documentation

Coordinate clinical projects and related follow-up activities

Responsibilities

  • Support indication managers in validating clinical claims
  • Review clinical literature and support literature searches
  • Identify clinical evidence gaps together with internal stakeholders

Requirements

  • Support evidence-based communication and scientific messaging
  • Compile and support clinical case reports and clinical documentation
  • Coordinate clinical projects and related follow-up activities

EU Requirements

Job Details

Posted13 June 2026
Closes13 July 2026
Work ModeHybrid

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