Yacht Life Sciences has a vacancy for a Clinical Registry Specialist at our client, a global biotechnological company.
As a Clinical Registry Specialist you are a member of the enterprise wide Clinical Registry team and can support pharma, consumer and/or medical devices operating companies with their clinical trial data disclosure obligations. The team, located in the US, Europe and Asia (third party), is responsible for ensuring that accurate, validated and consistent clinical trial data is posted on clinical trial registries worldwide.
As a Clinical Registry Specialist, you:
Non Technical Skills and Additional Details:
You must be strong multitasker, used to a complex, non-standard work environment whilst maintaining highest admin record standards for 'reproducibility' of trials. We are open to candidates with the right background (CTA-GTM/Regulatory Submission experience) and skill-set.
Technology experience and skills:
This concerns a secondment contract via Yacht for 1 year. Full-time (40h) is strongly preferred, working 32 or 36 hours per week can be discussed. We will offer a competitive benefits package in line with the seniority of the position (salary between 3000 and 4000 euro gross per 4-week period). You will become a member of a strong professional network who shares your education, ambitions and competencies. This will enable you to interact with your colleagues and become a member of the YACHT network, which stretches the Life Science industry. You will be challenged by your peers and will be able to follow courses and training via our Yacht Academy and keep your knowledge and skills up-to-date: boosting your career through personal and scientific growth.