- Ensure timely execution of assigned clinical review activities through efficient and effective use of internal resources and systems, as well as external parties
- Writing literature review plans and literature review reports and conducting or supervising literature reviews, assessments and analyses
- Act as scientific advisor and reviewer for publications on performance and safety of DORC products
- (Co-)author publications on behalf of DORC
- (Co-)author clinical evaluation plans and reports
- Preparation of post-market clinical follow-up (PMCF) plans and reports
- Timely escalation and resolution of quality or compliance issues
- Minimum of a bachelor's degree in a medical, biomedical or medical technology field, or completed training as an optometrist or orthoptist
- At least 2 years' experience in a similar role
- Familiar with clinical evaluation requirements and able to translate these into pragmatic guidelines for the organisation
- Sufficient knowledge of statistics to assess data analysis and statistical methodology in scientific publications for scientific validity
- Ability to perform multiple tasks simultaneously and manage projects methodically based on business priorities and available resources
- Ability to critically assess publications and documentation for scientific reliability
- Experience in conducting science-based literature reviews
- Self-motivated and able to work independently in a geographically separated, multinational and multifunctional team environment
- Experience in technical and scientific writing
- Effective collaboration within a diverse network of strong personalities
- Open to improvement opportunities and change to strive for world-class compliance performance
- Ability to think creatively and proactively identify alternative solutions to problems
- High ethical standards and personal integrity
- Good communication and interpersonal skills
- Fluent in English (both written and oral)
- Advanced level in Microsoft Office suite applications
Does working for you mean working together? Realising surgical devices together that help to make people see again? With a hands-on and both legs on the ground mentality? Do you want to work for an organisation where you get freedom and responsibility? Where you are fully stimulated to come up with new ideas? And where innovation, quality and technology are woven into the DNA? Then DORC is the place for you.
Would you like to know more about working at DORC? Then read on here.
What does DORC have to offer you?
At DORC, you play at top level. It is therefore only logical that we reward you as a top player. You can expect the following:
- 27 holidays for a 40-hour full-time job
- 8% holiday pay
- 13th month
- Bonus scheme
- A full-time salary between € 4,250 and € 5,320 gross per month. That's above average, but that's what you're worth!
- A travel allowance of €0.23/km
- The ability to work up to 50% from home if that suits
- And a non-contributory pension, which means you will receive a substantially higher net salary
What else can you expect from us? Every opportunity to learn and grow. Your own laptop and smartphone. And a fantastic company restaurant full of delicious, fresh products.
Did you know ...?
DORC, short for Dutch Ophthalmic Research Center, manufactures equipment, instruments and liquids used in eye surgery.
DORC is a ZEISS company, an internationally leading technology enterprise that develops, manufactures and sells highly innovative products and solutions in a variety of business fields, such as medical technology. As a company wholly owned by a foundation, ZEISS is rooted in and committed to responsibility in all its activities.
Will you be our new Clinical Evaluation Officer?
Are you up for this? Then apply directly via the red button! Do you still have questions? Then contact Monique Meiling our Global Recruiter: m.meiling@dorcglobal.com.