About the role
- Work closely with cross-functional teams to develop post market clinical evidence generation strategies
- Facilitate clinical evidence reviews with cross functional team
- Develop and write high quality Post-market Clinical Follow-up (PMCF) plans and reports
- Support development and drafting of clinical study protocols, registry plans, epidemiology studies
- Review summaries of clinical evidence and PMCF strategies
- Foster relationships with surgeons, hospitals and research teams
- Develop strong collaborative relationships with the study core team
- Partner with the Contracts and Payments team to ensure timely execution of all study agreements
- Support clinical scientific discussions with internal stakeholders
- Contribute to appropriate interpretation and dissemination of all evidence generated
- Develop a strong understanding of the orthopedic device product portfolio
Requirements
- A Master’s degree in Biological Science or related discipline
- Minimum of 4 years’ experience in the medical device industry or healthcare field
- Advanced technical writing skills
- Clinical expertise in the medical device sector
- Proven experience in conducting clinical studies, registries particularly in the field of orthopaedics
- Strong project management skills required
- Excellent communication skills
- Flexible working environment
- Professional development opportunities
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical evidence generationtechnical writingclinical study protocolsregistry plansepidemiology studiesPost-market Clinical Follow-up (PMCF)clinical studiesorthopaedics
Soft skills
collaborationrelationship buildingproject managementcommunication
Certifications
Master’s degree in Biological Science